Class 11 Chemistry Competency Based Question Bank With Answer Key & Structured Explanation 4 Chemical Bonding and Molecular Structure Questions
Class 11 Chemistry Competency Based Question Bank With Answer Key & Structured Explanation 4 Chemical Bonding and Molecular Structure Questions
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a) b) c) d)
a) b) c) d)
can be assigned to
a) O2 b) O+2 c) O−2 d) O2−
2
60. Some of the properties of the two species, NO− +
3 and H3 O are described below. Which one of them is
correct?
a) Dissimilar in hybridization for the central atom with different structure
b) Isostructural with same hybridization for the central atom
c) Isostructural with different hybridization for the central atom
d) Similar is hybridization for the central atom with different structure
61. 6, 6
a) 6, 6 b) 6, 6 c) 6, 6 d) 6, 6
62. Greater the dipole moment:
a) Greater is the ionic nature
b) Lesser the polarity
c) Smaller the ionic nature
d) None of these
63. H−B−H bond angle in BH4− is:
a) 180 b) 120 c) 109 d) 90
64. Which of the following molecular orbitals has two nodal planes?
a) 𝜎2𝑝𝑥 b) 𝜋2𝑝𝑦 c) 𝜋 ∗ 2𝑝𝑦 d) 𝜎 ∗ 2𝑝𝑥
65. The common feature among the species CN− , CO and NO+ are:
a) Bond order three and b) Bond order three and c) Bond order two and π- d) Isoelectronic and weak
isoelectronic weak field ligands acceptors field ligands
66. Hydrogen bonding is maximum in
a) C2 H5 OH b) CH3 OCH3 c) (CH3 )2 C = O d) CH3 CHO
67. The O—H bond distance in water molecule is:
a) 1.0Å b) 1.33 Å c) 0.96 Å d) 1.45 Å
68. 2+
O2 has a bond order of
a) 1 b) 2 c) 3 d) 4
69. Which among the following molecules/ ions is diamagnetic?
a) Super oxide ion
b) Oxygen
c) Carbon molecule
d) Unipositive ion of N2 molecule
70. The enolic form of acetone contains
a) 9 sigma bonds, 1 pi bond and two lone pairs
b) 8 sigma bonds, 2 pi bond and two lone pairs
c) 10 sigma bonds, 1 pi bond and one lone pairs
d) 9 sigma bonds, 2 pi bond and one lone pairs
71. Which of the following are isoelectronic and isostructural?
NO− 2− −
3 , CO3 , ClO3 , SO3
a) NO− 3 , CO3
2−
b) SO3 , NO−
3 c) ClO− 2−
3 , CO3 d) CO2−3 , SO3
72. Which of the following is paramagnetic with bond order 0.5?
a) F2 b) H2+ c) N2 d) O−2
73. Water has high heat of vaporization due to:
a) Covalent bonding b) H-bonding c) Ionic bonding d) None of these
74. The C – H bond distance is the longest in
a) C2 H6 b) C2 H2 c) C2 H2 Br2 d) C2 H4
75. If the electronegativity difference between two atoms 𝐴 and 𝐵 is 2.0, then the percentage of covalent
character in the molecule is
a) 54% b) 46% c) 23% d) 72%
−
76. Structure of ICl2 is:
a) Trigonal
b) Octahedral
c) Square planar
d) Distorted trigonal pyramidal
77. Polar covalent compounds are soluble in:
a) Polar solvents b) Non-polar solvents c) Concentrated acids d) All solvents
−
78. N2 Ois isoelectronic to CO2 and N3 . Which of the following is the structure of N2 O?
a) b) N − O − N c) N − O − N d)
a) 1 b) 2 c) 3 d) 1/3
117. A compound contains X, Y and Z atoms. The oxidation states of X, Y and Z are +2, +2 and -2 respectively.
The possible formula of the compound is
a) 𝑋𝑌𝑍2 b) 𝑌2 (𝑋𝑍3 )2 c) 𝑋3 (𝑌4 𝑍)2 d) 𝑋3 (𝑌𝑍4 )3
118. Which one of the following is a non-polar molecule?
a) CCl4 b) CHCl3 c) CH2 Cl2 d) CH3 Cl
119. Which one of the following has the regular tetrahedral structure?
(Atomic numbers B = 5, S = 16, Ni = 28, Xe = 54)
a) XeF4 b) SF4 c) BF4− d) [Ni(CN)3 ]2−
120. If the dipole moment of toluene and nitro-benzene are 0.43 D and 3.93 D, then what is the expected dipole
moment of p-nitro toluene?
a) 3.50 D b) 2.18 D c) 4.36 D d) 5.30 D
121. Which of the following is most stable?
a) Pb2+ b) Ge2+ c) Si2+ d) Sn2+
122. In which of the following compound 𝑠𝑝2 hybridisation is absent?
a) CH2 = CH − CH = CH2 b) CH ≡ C − CH2 − CH3
c) CH2 − CH = CH2 d) CH2 = CH − CH2 − CH3
123. Which one of the following pairs of species has the same bond order:
a) NO+ and CN+ b) CN− and NO+ c) CN− and CN + d) O−2 and CN
−
a) b)
c) d)
a) 𝑠𝑝 b) 𝑠𝑝 2 c) 𝑠𝑝3 d) 𝑑𝑠𝑝2
134. Electron deficient species are known as:
a) Lewis acids b) Hydrophilic c) Nucleophiles d) Lewis bases
135. The molecule having three folds of axis of symmetry is:
a) NH3 b) PCl5 c) SO2 d) CO2
136. The structure of ICl−
2 is:
a) Trigonal
b) Octahedral
c) Square planar
d) Distorted trigonal bipyramid
137. Among the following the molecule with the highest dipole moment is
a) CH3 Cl b) CH2 Cl2 c) CHCl3 d) CCl4
138. Which of the following isnot isostructural with SiCl4 ?
a) PO3−
4 b) NH4+ c) SCl4 d) SO2−
4
139. A molecule which cannot exist theoretically is:
a) SF4 b) OF2 c) OF4 d) O2 F2
140. An atom 𝑋 has three valence electrons and atom 𝑌 has six valence electrons. The compound formed
between them will have the formula
a) 𝑋2 𝑌6 b) 𝑋𝑌2 c) 𝑋2 𝑌3 d) 𝑋3 𝑌2
141. Which one is polar molecule among the following?
a) CH4 b) CCl4 c) CO2 d) H2 O
142. Shape of molecules is decided by:
a) Sigma bond
b) π-bond
c) Both sigma and π-bonds
d) Neither sigma nor π-bonds
143. The shape of carbon dioxide is
a) Pyramidal b) Tetrahedral c) Planar d) linear
144. The correct ionic radii order is:
a) N3− > O2− > F − > 𝑁a+ > 𝑀g 2+ > 𝐴l3+
b) N3− > Na+ > O2− > F − > 𝑀g 2+ > 𝐴l3+
c) Na+ > O2− > N3− > F − > 𝑀g 2+ > 𝐴l3+
d) O2− > F − > 𝑁a+ > N3− > 𝑀g 2+ > 𝐴l3+
145. Which is not linear?
a) CO2 b) HCN c) C2 H2 d) H2 O
146. Hybridisation of oxygen in diethyl ether is
a) Sp b) 𝑠𝑝 2 c) 𝑠𝑝3 d) 𝑠𝑝3 𝑑
147. What is the effect of more electronegative atom on the strength of ionic bond?
a) Increases b) Decreases c) Remains the same d) None of these
148. Which of the following two are isostructural?
a) XeF2 , IF2− b) NH3 , BF3 c) CO2− 2−
3 , SO3 d) PCl5 , ICl5
149. NF3 is:
a) Non-polar compound
b) Electrovalent compound
c) Having low value of dipole moment than NH3
d) Having more dipole moment than NH3
150. Molecular size of ICl and Br2 is nearly same, but boiling point of ICl is about 40C higher than Br2 . This
might be due to:
a) I—Cl bond is stronger than Br—Br bond
b) Ionisation energy of I < ionisation energy of Br
c) ICl is polar where as Br2 is non-polar
d) The size of I > size of Br
151. Which molecule is linear?
a) H2 S b) NO2 c) ClO2 d) CO2
152. Which of the following shows minimum melting point?
a) Naphthalene b) Diamond c) NaCl d) Mn
153. Which of the following does not have a lone pair on the central atom?
a) NH3 b) PH3 c) BF3 d) PCl3
154. Molecular orbital theory was given by
a) Kossel b) Mosley c) Mulliken d) Werner
155. NH3 has a net dipole moment, but boron trifluoride (BF3 ) has zero dipole moment, because:
a) B is less electronegative than N
b) F is more electronegative than H
c) BF3 is pyramidal while NH3 is planar
d) NH3 is pyramidal while BF3 is trigonal planar
156. Proton plays an important role in…bonding.
a) Electrovalent b) Hydrogen c) Covalent d) Coordinate
157. Which represents a collection of isoelectronic species?
a) Be, Al3+ , Cl− b) Ca2+ , Cs+ , Br c) Na+ , Ca2+ , Mg 2+ d) N3− , F − , Na+
158. An electrovalent compound does not exhibit space isomerism due to:
a) Presence of ions
b) High melting point
c) Strong electrostatic forces between constituent ions
d) Non-directional nature of electrovalent bond
159. In which molecule Sulphur atom is not 𝑠𝑝3-hybridized?
a) SO2−4 b) SF4 c) SF2 d) None of these
160. In which one of the following species, the central atom has the type of hybridization which is not the same
as that present in other three?
a) SF4 b) I3− c) SbCl2−
5 d) PCl5
161. The radii of F, F , O and O are in the order of:
− 2−
a) O2− > F − > 𝐹 > 𝑂 b) F − > O2− > 𝐹 > 𝑂 c) O2− > 𝑂 > F − > 𝐹 d) O2− > F − > 𝑂 > 𝐹
162. The correct order of decreasing second ionisation enthalpy of Ti(22), V(23), Cr(24) and Mn(25) is:
a) V > 𝑀𝑛 > 𝐶𝑟 > 𝑇𝑖 b) Mn > 𝐶𝑟 > 𝑇𝑖 > 𝑉 c) Ti > 𝑉 > 𝐶𝑟 > 𝑀𝑛 d) Cr > 𝑀𝑛 > 𝑉 > 𝑇𝑖
163. How many 𝜎 and 𝜋-bonds are present in given compound?
Ph − CH = C − C2 H5
|
CH3
a) 19 𝜎 and 4 𝜋 − bonds b) 22 𝜎 and 4 𝜋 − bonds
c) 25 𝜎 and 4 𝜋 − bonds d) 26 𝜎 and 4 𝜋 − bonds
164. C − Cl bond is stronger than C – Ibond, because
a) C − Cl bond is more ionic than C – I b) C − Cl bond is polar covalent bond
c) C − Cl bond is more covalent than C – I d) C − Cl bond length is longer than C – I
165. The ICl molecule is:
a) Purely covalent
b) Purely electrovalent
c) Polar with negative end on chlorine
d) Polar with negative end on iodine
166. Which of the following silver salts is insoluble in water?
a) AgClO4 b) Ag 2 SO4 c) AgF d) AgNO3
167. Silicon has 4 electrons in the outermost orbit. In forming the bond:
a) It gains electrons b) It losses electrons c) It shares electrons d) None of these
168. The shape of gaseous SnCl2 is
a) Tetrahedral b) Linear c) Angular d) 𝑇-shape
169. Chlorine atom tends to acquire the structure of:
a) He b) Ne c) Ar d) Kr
170. The d – orbital involved in 𝑠𝑝3 d – hybridisation is
a) 𝑑𝑥 2−𝑦2 b) 𝑑𝑥𝑦 c) 𝑑𝑧 2 d) 𝑑𝑧𝑥
+
171. When O2 is converted into O2 ;
a) Both paramagnetic character and bond order increase
b) Bond order decreases
c) Paramagnetic character increases
d) Paramagnetic character decreases and the bond order increases
172. Intramolecular hydrogen bond is present in
a) Water b) o-nitrophenol c) p-nitrophenol d) methylamine
173. A pair of compounds which have odd electrons in the group NO, CO, ClO2 , N2 Os , SO2 and O2are
a) NO and ClO2 b) COI and SO2 c) ClO2 and CO d) SO2 andO3
174. According to VSEPR theory the repulsion between different pair (lone or bond) of electrons obey the order
a) lpbplplpbpbp b) lpbpbpbplplp
c) lplplpbpbpbp d) bpbplplplpbp
175. The bond between two identical non-metal atoms has a pair of electrons:
a) Unequally shared between the two
b) Equally shared between the two
c) Transferred fully from one atom to another
d) None of the above
176. The bond angle in AsH3 is greater than that in
a) NH3 b) H2 O c) BCl3 d) None of these
177. The correct order of increasing electropositive character among Cu, Fe and Mg is:
a) Cu ≈ Fe < 𝑀𝑔 b) Fe < 𝐶𝑢 < 𝑀𝑔 c) Fe < 𝑀𝑔 < 𝐶𝑢 d) Cu < 𝐹𝑒 < 𝑀𝑔
178. H—O—H bond angle in H2 O is 104.5 and not 10928′ because of:
a) High electronegativity of oxygen
b) Bond pair-bond pair repulsion
c) Lone pair-lone pair repulsion
d) Lone pair-bond pair repulsion
179. The bond order in O+ 2 is equal to bond order in:
+
a) N2 b) CN− c) CO d) NO+
180. The electron affinity for inert gases is likely to be:
a) High b) Small c) Zero d) Positive
181. The true statements from the following are
1.PH5 and BiCl5 do not exist
2.𝑝𝜋 − 𝑑𝜋 bond is present in SO2
3.Electrons travel at the speed of light
4.SeF4 and CH4 have same shape
5.I3+ has bent geometry
a) 1,3 b) 1,2,5 c) 1,3,5 d) 1,2,4
182. 1,3-butadiene has:
a) 6σ and 2π-bonds b) 2σ and 2π-bonds c) 9σ and 2π-bonds d) 6σ and 2π-bonds
183. The bond between atoms of two elements of atomic number 37 and 53 is:
a) Covalent b) Ionic c) Coordinate d) Metallic
184. In methane the bond angle is
a) 180° b) 90° c) 109° d) 120°
185. One would expect the elemental form of Cs at room temperature to be:
a) A network solid b) A metallic solid c) Non-polar liquid d) An ionic liquid
186. Which of the following is false?
a) Glycerol has strong hydrogen bonding
b) Glycol is a poisonous alcohols
c) Waxes are esters of higher alcohols with higher acids
d) Alkyl halides have higher b.p. than corresponding alcohols
187. Ionic radii are:
1
a) ∝
effective nuclear charge
1
b) ∝ (
effective nuclear charge)2
c) ∝ effective nuclear charge
d) ∝ (effective nuclear charge)2
188. Which of the following statements is incorrect?
a) He2 does not exist because its bond order is zero
b) O2 , O− +
2 and O2 are all paramagnetic
c) Any two atomic orbitals can combine to form two molecular orbitals
d) 𝜋(2𝑝𝑥 ) and 𝜋(2𝑝𝑦 )are degenerate molecular orbitals
189. Which of the following pairs will from the most stable ionic bond?
a) Na and Cl b) Mg and F c) Li and F d) Na and F
190. Among NaF, NaCl NaBr and NaI, the NaF has highest melting point because:
a) It has maximum ionic character
b) It has minimum ionic character
c) It has associated molecules
d) It has least molecular weight
191. The planar structure of BF3 can be explained by the fact that BF3 is
a) sp hybridized b) 𝑠𝑝 2 hybridised c) 𝑠𝑝3 hybridised d) 𝑠𝑝3 𝑑hybridized
192. The correct order of bond order value among the following is
(i) NO− (ii) NO+
(iii)NO (iv) NO2+
2−
(v) NO
a) (i) < (iv) < (iii) < (ii) < (𝑣) b) (iv) = (ii) < (i) < (v) < (𝑖𝑖𝑖)
c) (v) < (i) < (iv) = (iii) < (𝑖𝑖) d) (ii) < (iii) < (iv) < (i) < (𝑣)
193. The bond between chlorine and bromine in BrCl3 is:
a) Ionic
b) Non-polar
c) Polar with negative end on Br −
d) Polar with negative end on Cl−
194. Which of the following has regular tetrahedral shape?
a) [Ni(CN)4 ]2− b) SF4 c) [BF4 ]− d) XeF4
195. Which of the following will have large dipole moment?
a) b) c) d)
a) O2− −
2 > O2 > O2 > O2
+
b) O+ −
2 > O2 > O2 > O2
2−
c) O2 > O− 2−
2 > O2 > O2
+
d) O− 2− +
2 > O2 > O2 > O2
222. The shape of XeF4 molecule and hybridisation of xenon in it are
a) Tetrahedral and 𝑠𝑝3 b) Square planar and 𝑑𝑠𝑝2
c) Square planar and 𝑠𝑝3 𝑑2 d) Octahedral and 𝑠𝑝3 𝑑2
−
223. In H2 ion, the bond order is:
a) Zero b) 1/2 c) -1/2 d) 1
224. H-bonding is not present in:
a) Glycerine b) Water c) H2 S d) HF
225. In which of the following gaseous molecules, the ionic character of the covalent bond is greatest?
a) HCl b) HBr c) HI d) HF
226. The angle between the overlapping of one 𝑠-orbital and one 𝑝-orbital is:
a) 180 b) 120 c) 10928′ d) 12060′
227. How many bonds are there in?
a) 14 σ, 8π b) 18 σ, 8π c) 19 σ, 4π d) 14 σ, 2π
228. Which is the correct statement about σ and π molecular orbitals? Statements are
(i) π-bonding orbitals are ungerade
(ii) π-antibondingorbitals are ungerade
(iii) σ-antibondingorbitals are gerade
a) (i) only b) (ii) and (iii) only c) (iii) only d) (ii) only
229. Among the following statement, the correct statement about PH3 and NH3 is:
NH3 is a better electron donor because the lone pair of electron occupies spherical 𝑠-orbital and is less
a)
directional
PH is a better electron donor because the lone pair of electron occupies 𝑠𝑝3 -orbital and is more
b) 3
directional
NH3 is a better electron donor because the lone pair of electron occupies 𝑠𝑝3 -orbital and more
c)
directional
PH is a better electron donor because the lone pair of electron occupies spherical 𝑠-orbital and is less
d) 3
directional
230. Which is expected to have linear structure?
a) SO2 b) CO2 c) CO2−3 d) SO2−
4
231. The bond angle in PH3 is:
a) Much lesser than NH3 b) Equal to that in NH3 c) Much greater than in d) Slightly more than in
NH3 NH3
232. Carnallite in solution in water shows the properties of
a) K + , Mg 2+ , Cl− b) K + , Cl− , SO2−
4 , Br
−
c) K + , Mg 2+ , CO2− 3 d) K + , Mg 2+ , Cl− , Br −
233. A simple of a coordinate covalent bond is exhibited by
a) HCl b) NH3 c) C2 H2 d) H2 SO4
234. In the series ethane, ethylene and acetylene, the C—H bond energy is:
a) The same in all the three compounds
b) Greatest in ethane
c) Greatest in ehtylene
d) Greatest in acetylene
235. In which molecule the van der Waals’ force is likely to be the most important in determining the m.p. and
b.p.?
a) Br2 b) CO c) H2 S d) HCl
236. Identify the wrong statement in the following:
a) Atomic radius of the elements increases as one moves down the first group of the periodic table
b) Atomic radius of the elements decreases as one moves across from left to right in the 2nd period of the
periodic table
c) Amongst isoelectronic species, smaller the positive charge on the cation, smaller is the ionic radius
d) Amongst isoelectronic species, greater the negative charge on the anion, larger is the ionic radius
237. (I)1, 2-dihydroxy benzene
(II) 1, 3-dihydroxy benzene
(III) 1, 4-dihydroxy benzene
(IV) Hydroxy benzene
The increasing order of boiling points of above mentioned alcohols is
a) I < 𝐼𝐼 < 𝐼𝐼𝐼 < 𝐼𝑉 b) I < 𝐼𝐼 < 𝐼𝑉 < 𝐼𝐼𝐼
c) IV < 𝐼 < 𝐼𝐼 < 𝐼𝐼𝐼 d) IV < 𝐼𝐼 < 𝐼 < 𝐼𝐼𝐼
238. Dipole moment is shown by
a) cis- 1, 2-dichloro ethane b) trans-1, 2-dichloro ethane
c) trans-1 2-dichloro-2 peptene d) Both (a) and (c)
239. Compounds formed by 𝑠𝑝 𝑑 -hybridization will have configuration:
3 2
a) Square planar
b) Octahedral
c) Trigonal bipyramidal
d) Pentagonal bipyramidal
240. In which molecular are all atoms coplanar?
a) PF3 b) NH3 c) BF3 d) CH4
241. The AsF5 molecule is trigonal bipyramidal.The hybrid orbitals used by the As atoms for bonding are
a) 𝑑𝑥 2−𝑦2 , 𝑑𝑧 2 , 𝑠, 𝑃𝑥 , 𝑃𝑦 b) 𝑑𝑥𝑦 , 𝑠, 𝑃𝑥 , 𝑃𝑧 c) 𝑠, 𝑃𝑥 , 𝑃𝑦 , 𝑃𝑧 , 𝑑𝑧 2 d) 𝑑𝑥 2−𝑦2 , 𝑠, 𝑃𝑥 , 𝑃𝑦
+
242. The bond order of N2 is
a) 1.5 b) 3.0 c) 2.5 d) 2.0
243. CO2 is isostructural with
a) C2 H2 b) SnCI2 c) NO2 d) MgCI2
244. The compound with the maximum dipole moment among the following is:
a) 𝑝-dichlorobenzene b) 𝑚-dichlorobenzene c) 𝑜-dichlorobenzene d) Carbon tetrachloride
245. Which of the following bonds require the largest amount of energy to dissociate the bond concerned?
a) H—H bond in H2 b) C—H bond in CH4 c) N ≡ N bond in N2 d) O = O bond in O2
246. The sequence that correctly describes the relative bond strength pertaining to oxygen molecule and its
cation or anion is
a) O2− −
2 > O2 > O2 > O2
+
b) O2 > O+ −
2 > O2 > O2
2−
a) CO2 b) SO2 c) N2 O d) CO
263. The increasing order of the ionic radii of the given isoelectronic species is:
a) S2− , Cl− , Ca2+ , K + b) Ca2+ , K + , Cl− , S2− c) K + , S2− , Ca2+ , Cl− d) Cl− , Ca2+ , K + , S2−
264. Which cannot exist on the basis of M.O. theory?
a) C2 b) He+2 c) H2+ d) He2
265. Which of the following does not involve covalent bond?
a) PH3 b) CsF c) HCl d) H2 S
266. B10 C2 H12 is isoelectronic with
+
2−
a) B12 H12 b) B12 H12 c) B12 H12 d) B12 H122+
267. The electronegativity of A and B are 1.20 and 4.0 respectively. Therefore, ionic character in 𝐴 − 𝐵 bond
will be
a) 50% b) 43% c) 53.3% d) 72.23%
268. During the formation of a chemical bond
a) Electron-electron repulsion becomes more than b) Energy of the system does not change
the nucleus-electron repulsion attraction
c) Energy increases d) Energy decreases
269. The number of ions formed when a molecule of K 4 Fe(CN)6 dissociates is:
a) 4 b) 5 c) 6 d) 2
270. Pair of species having identical shapes for molecules is
a) CF4 , SF4 b) BF3 , PCl3 c) XeF2 , CO2 d) PF5 , IF7
271. An example of a polar covalent compound is
a) KCl b) NaCl c) CCl4 d) HCl
272. Which is not an exception to octet rule?
a) BF3 b) SnCl4 c) BeI2 d) ClO2
273. The molecules having dipole moment are:
a) 2, 2-dimethylpropane
b) 𝑇𝑟𝑎𝑛𝑠-3-hexene
c) 𝑇𝑟𝑎𝑛𝑠-2-pentene
d) 2, 2, 3, 3-tetramethylbutane
274. Which of the following species has a bond order other than 3?
a) CO b) CN− c) NO+ d) O+2
275. Which of the following is planar?
a) XeF2 b) XeO3 F c) XeO2 F2 d) XeF4
276. Among the following species, identify the pair having same bond order CN− , O− 2 , NO +
, CN +
a) CN− and O− 2 b) O−2 and NO
+
c) CN− and NO+ d) CN− and CN +
277. The bond angle and dipole moment of water respectively, are
a) 109.5°, 1.84 D b) 107.5°, 1.56 D c) 104.5°, 1.84 D d) 102.5°, 1.56 D
278. The correct order of increasing bond angles in the following species is:
a) Cl2 O < 𝐶𝑙O2 < 𝐶𝑙O− 2 b) ClO2 < 𝐶l2 O < 𝐶𝑙O− 2 c) Cl2 O < 𝐶𝑙O−2 < 𝐶𝑙O2 d) ClO− 2 < 𝐶l2 O < 𝐶𝑙O2
279. Which compound shows hydrogen bonding?
a) 𝑅CH2 NHCH3 b) 𝑅CH2 CHO c) C2 H6 d) HCl
280. Chlorine atom differs from chloride ion in the number of:
a) Protons
b) Neutrons
c) Electrons
d) Protons and electrons
281. What is the reason for unusual high b.p. of water?
a) Due to the presence of H + and OH − ions in water b) Due to dipole – dipole interactions
c) Due to London forces d) Strong London Forces
282. The increasing order of the first ionization enthalpies of the elements B, P, S and F (lower first) is:
a) F < 𝑆 < 𝑃 < 𝐵 b) P < 𝑆 < 𝐵 < 𝐹 c) B < 𝑃 < 𝑆 < 𝐹 d) B < 𝑆 < 𝑃 < 𝐹
283. The IP1 , IP2 , IP3 , IP4 , and IP5 of an element are 7.1, 14.3, 34.5, 46.8, 162.2 eV respectively. The element is
likely to be:
a) Na b) Si c) F d) Ca
284. Which of the following is paramagnetic?
a) B2 b) C2 c) N2 d) F2
285. Ionization potential of Na would be numerically the same as:
a) Electron affinity of Na+
b) Electronegativity of Na+
c) Electron affinity of He
d) Ionization potential of Mg
286. Which one of the following conversions involve change in both hybridisation and shape?
a) CH4 ⟶ C2 H6 b) NH3 ⟶ NH4+ c) BF3 ⟶ BF4− d) H2 O ⟶ H3 O+
287. According to MO theory,
a) O+2 is paramagnetic and bond order greater than O2
b) O+2 is paramagnetic and bond order less than O2
c) O+2 is diamagnetic and bond order is less than O2
d) O+2 is diamagnetic and bond order is more than O2
288. If the molecule of HCl were totally polar, the expected value of dipole moment is 6.12 D (dbye), but the
experimental value of dipole moment was 1.03 D. Calculate the percentage ionic character
a) 17 b) 83 c) 50 d) Zero
289. The order of first electron affinity of O, S and Se is:
a) O > 𝑆 > 𝑆𝑒 b) S > 𝑂 > 𝑆𝑒 c) Se > 𝑂 > 𝑆 d) Se > 𝑆 > 𝑂
290. The nodal plane in the 𝜋-bond of ethane is located in:
a) The molecular plane
b) A plane parallel to the molecular plane
c) A plane perpendicular to the molecular plane which bisects the carbon-carbon σ-bond at right angle
d) A plane perpendicular to the molecular plane which contains the carbon-carbon σ-bond
291. The correct electronegativity order is:
a) C, N, Si, P b) N, Si, C, P c) Si, P, C, N d) P, Si, N, C
292. The pair of species having identical shapes for molecules of both species is
a) CF4 , SF4 b) XeF2 , CO2 c) BF3 , PCl3 d) PF5 , IF5
293. Amongst the following, the molecule that is linear is
a) SO2 b) CO2 c) ClO2 d) NO2
294. Using MO theory predict which of the following species has the shortest bond length?
a) O2+
2 b) O+2 c) O−2 d) O2−
2
295. The hybridisation of carbon atom in benzene is?
a) 𝑠𝑝 b) 𝑠𝑝 2 c) 𝑠𝑝3 d) 𝑑𝑠𝑝2
296. Bond angle between two hybrid orbitals is 105. Hybrid character orbital is:
a) Between 20-21% b) Between 19-20% c) Between 21-22% d) Between 22-23%
297. KFcombines with HF to form KHF2. The compound contains the species:
a) K + , F − and H + b) K + , F − and HF c) K + and [HF2 ]− d) [KHF]+ and F −
298. 𝑜-hydroxy benzaldehyde, although contains enolic group but does not give test of group with FeCl3
because:
a) It is steam volatile
b) Of intermolecular H-bonding
c) Of intramolecular H-bonding
d) All of the above
299. Iron is tougher than sodium because:
a) Iron atom is smaller
b) Iron atoms are more closely packed
c) Metallic bonds are stronger in iron
d) None of the above
300. Correct order of bond angles in NH3 , PCl3 and BCl3 is
a) PCl3 > 𝑁H3 > 𝐵𝐶l3 b) NH3 > 𝐵𝐶l3 > 𝑃𝐶l3
c) NH3 > 𝑃𝐶l3 > 𝐵𝐶l3 d) BCl3 > 𝑁H3 > 𝑃𝐶l3
301. The number of π- bonds present in propyne is
a) 4 b) 1 c) 3 d) 2
302. A bond with maximum covalent character between non-metallic elements is formed:
a) Between identical atoms
b) Between chemically similar atoms
c) Between atoms of widely different electro-negativities
d) Between atoms of the same size
303. The compound in which underlined carbon uses only its 𝑠𝑝3 hybrid orbitals for bond formation is
a) CH3 COOH b) CH3 CONH2 c) CH3 CH2 OH d) CH2 CH = CH2
304. Consider the following compounds
(i) chloroethene (ii) benzene
(iii) 1, 3-butadiene (iv) 1,3,5 – hexatriene
All the carbon atoms are 𝑠𝑝2 hybridised in
a) (i), (iii), (iv) only b) (i), (ii) only c) (ii), (ii), (iv) only d) (i), (ii), (iii) and (iv)
305. When ionic compounds get dissolved in water:
a) They involve heat changes
b) Inter-ionic attraction is reduced
c) Ions show dipole-ion attraction with water molecules
d) All are correct
306. Pick the odd one out (The one having zero dipole moment):
a) NH3 b) H2 O c) BCl3 d) SO2
307. Which of the following shows minimum bond angle?
a) H2 O b) H2 Se c) H2 S d) H2 Te
308. Among the following isostructural compounds, identify the compound which has the highest lattice energy
a) LiF b) LiCl c) NaCl d) MgO
309. Which species is diamagnetic in nature?
a) He+ 2 b) H2 c) H2+ d) H2−
310. Which of the following compounds would have the highest boiling point?
a) CH3 CH2 CH2 CH3 b) CH3 NH2 c) CH3 OH d) CH2 F2
311. Hybridisation of central atom in NF3 is
a) 𝑠𝑝3 b) 𝑠𝑝 c) 𝑠𝑝2 d) 𝑑𝑠𝑝2
312. Which of the compounds has highest boiling point?
a) Acetone b) Diethyl ether c) Methanol d) Ethanol
313. The number and type of bonds between two carbon atoms in CaC2 are:
a) One sigma (σ) and one pi (π)-bond
b) One sigma (σ) and two pi (π)-bonds
c) One sigma (σ) and one and a half pi (π)-bond
d) One sigma (σ) bond
314. Which of the following hydrogen bonds are strongest in vapour phase?
a) HF---HF b) HF---HCl c) HCL---HCl d) HF---Hi
315. The bond angle and hybridization in ether (CH3 OCH3 ) is:
a) 106 ͦ 51′ , 𝑠𝑝3 b) 104 ͦ 31 ′ , 𝑠𝑝3 c) 110 ͦ , 𝑠𝑝3 d) None of these
316. Which has the highest bond energy?
a) Hydrogen bond b) Triple bond c) Double bond d) Single bond
317. Among the following compounds the one that is polar and has central atom with 𝑠𝑝 2 -hybridisation is:
a) H2 CO3 b) SiF4 c) BF3 d) HClO2
318. The incorrect statement among the following is:
a) The first ionization potential of Al is less than the first ionization potential of Mg
b) The second ionization potential of Mg is greater than the second ionization potential of Na
c) The first ionization potential of Na is less than the first ionization potential of Mg
d) The third ionization potential of Mg is greater than the third ionization potential of Al
319. The bond angle is smallest in
a) H2 O b) H2 S c) BeCl2 d) N2 O
320. The number of electrons in the valence shell of sulphur in SF6 is
a) 12 b) 10 c) 8 d) 11
321. Acetic acid exists as dimer in benzene due to:
a) Condensation reaction
b) Hydrogen bonding
c) Presence of carboxyl group
d) Presence of hydrogen atom at α-carbon
322. The correct order of hybridization of the central atom in the following species NH3 , [PtCl4 ]2− , PCl5 and
BCl3 is:
a) 𝑑𝑠𝑝 2 , 𝑑𝑠𝑝3 , 𝑠𝑝2 , 𝑠𝑝3 b) 𝑠𝑝 3 , 𝑑𝑠𝑝2 , 𝑑𝑠𝑝3 , 𝑠𝑝2 c) 𝑑𝑠𝑝2 , 𝑠𝑝2 , 𝑠𝑝3 , 𝑑𝑠𝑝3 d) 𝑑𝑠𝑝2 , 𝑠𝑝3 , 𝑠𝑝 2 , 𝑑𝑠𝑝3
323. Chemical bond formation takes place when?
a) Energy is absorbed
b) Forces of attraction overcome forces of repulsion
c) Forces of repulsion overcome forces of attraction
d) Forces of attraction are equal to forces of repulsion
324. NH3 has higher boiling point than expected, because:
a) With water it forms NH4 OH
b) It has strong intermolecular hydrogen bonds
c) It has strong intermolecular covalent bonds
d) Its density decreases in freezing
325. Which of the following represents the Lewis structure of N2 molecule?
a) b) c) d)
a) 3 b) 2 c) 3/2 d) 1
332. Which is likely to have the highest melting point?
a) He b) CsF c) NH3 d) CHCl3
333. Which of the following are not correct?
a) Lone pair of electrons present on central atom can give rise to dipole moment
b) Dipole moment is vector quantity
c) CO2 molecule has dipole moment
d) Difference in electronegativities of combining atoms can lead to dipole moment
334. In the formation of N2+ from N2 , the electron is lost from:
a) a σ-orbital b) a π-orbital c) a σ∗ -orbital d) a π∗ -orbital
335. Bond angle of 109°28′ is found in
a) NH3 b) H2 O c) d)
336. The half of the difference between the number of electrons in bonding molecular orbitals and antibonding
molecular orbitals is known as:
a) Bond order b) Proton order c) Molecular order d) Electron order
337. Which of the following set contains species having same angle around the central atom?
a) SF4 , CH4 , NH3 b) NF3 , BCl3 , NH3 c) BF3 , NF3 , AlCl3 d) BF3 , BCl3 , BBr3
338. At ordinary temperature and pressure, among halogens, the chlorine is a gas, bromine is a liquid and
iodine is a solid. This is because:
a) The specific heat is in the order Cl2 > 𝐵r2 > I2
b) Intermolecular forces among molecules of chlorine are the weakest and those in iodine are the
strongest
c) The order of density is I2 > 𝐵r2 > 𝐶l2
d) The order of stability is Cl2 > 𝐵r2 > I2
339. Which of the following has lowest bond angle?
a) BeF2 b) H2 O c) NH3 d) CH4
340. Which of the following has shortest carbon-carbon bond length?
a) C6 H6 b) C2 H6 c) C2 H4 d) C2 H2
341. Which one of the following constitutes a group of the isoelectronic species?
a) C22− , O−
2 , CO, NO b) NO+ , C22− , CN− , N2 c) CN− , N2 , O2− 2−
2 , CO3 d) N2 , O− +
2 , NO , CO
342. The 𝑠𝑝 3 𝑑2 hybridisation of central atom of a molecule would lead to
a) Square planar geometry
b) Tetrahedral geometry
c) Trigonalbipyramidal geometry
d) Octahedral geometry
343. Methanol and ethanol are miscible in water due to:
a) Covalent character
b) Hydrogen bonding character
c) Oxygen bonding character
d) None of the above
344. The shape of ClF3 is
a) Distorted T- shape b) Pyramidal c) Tetrahedral d) Trigonal planar
345. Which are true statements among the following?
(1) PH5 and BiCl5 does not exist
(2 ) 𝑝𝜋—𝑑𝜋 bonds are present in SO2
(3) Electrons travel with speed of light
(4) SeF4 and CH4 has same shape
(5) I3+ has bent geometry
a) 1, 3 b) 1, 2, 5 c) 1, 3, 5 d) 1, 2, 4
−
346. The actual geometry of NO2 is
a) Planar b) Linear c) V-shape d) Tetrahedral
347. Which has the lowest anion to cation size ratio?
a) LiF b) NaF c) CsI d) CsF
348. The energy change accompanying the process given below is,
Na+ (g) + Cl− (g) ⟶ NaCl(𝑠):
a) Hydration energy b) Ionization energy c) Electron affinity d) Lattice energy
349. Which of the following has covalent bond?
a) Na2 S b) AlCl3 c) NaH d) MgCl2
350. The correct order in which the O − O bond length increases in the following is
a) O2 < O3 < H2 O2 b) H2 O2 < O3 < O2 c) O3 < O2 < H2 O2 d) O2 < H2 O2 < O3
351. N2 is less reactive than CN due to
−
a) Difference in spin quantum number b) Presence of more electrons in orbitals
c) Absence of dipole moment d) None of the above
+
352. According to molecular orbital theory for O2 :
a) Bond order is less than O2 and O+ 2 is paramagnetic
b) Bond order is more than O2 and O+ 2 is paramagnetic
+
c) Bond order is less than O2 and O2 is diamagnetic
d) Bond order is more than O2 and O+ 2 is diamagnetic
353. As compared to covalent compounds, electrovalent compounds generally have:
a) Low melting points and low boiling points
b) High melting points and high boiling points
c) Low melting points and high boiling points
d) High melting points and low boiling points
354. Which is present in peroxides?
a) O2 b) O2− c) O2−
2 d) O−2
355. Two hybrid orbitals have a bond angle of 120°. The percentage of𝑠 character in the hybrid orbital is nearly
a) 25% b) 33% c) 50% d) 66%
356. Which molecule is T-shaped?
a) BeF2 b) BCl3 c) NH3 d) ClF3
357. Which of the following is paramagnetic?
a) O2 b) CN− c) CO d) NO+
358. Dipole moment is highest for:
a) CHCl3 b) CH4 c) CHF3 d) CCl4
359. Which will not conduct electricity?
a) Aqueous KOH solution b) Fused NaCl c) Graphite d) KCl in solid state
360. The ionization potential order for which set is correct?
a) Li > 𝐾 > 𝐶𝑠 b) B > 𝐿𝑖 > 𝐾 c) Cs > 𝐿𝑖 > 𝐵 d) Cs < 𝐿𝑖 < 𝐾
361. The bond that determines the secondary structure of a protein is:
a) Coordinate bond b) Covalent bond c) Hydrogen bond d) Ionic bond
362. Molecular orbital theory was developed mainly by
a) Pauling b) Mulliken c) Thomson d) Pauling and Slater
363. Which species has lone pair on central atom?
a) CCl4 b) CH4 c) NH4+ d) H2 O
364. In which of the following molecules/ions are all the bonds not equal?
a) SF4 b) SiF4 c) XeF4 d) BF4−
365. Super octet molecule is:
a) F3 Cl b) PCl3 c) NH3 d) None of these
366. The number of unpaired electrons in a paramagnetic diatomic molecule of an element with atomic number
16 is:
a) 4 b) 1 c) 2 d) 3
367. Which of the following statement is not correct?
a) Hybridisation is the mixing of atomic orbitals prior to their combining into molecular orbitals
b) 𝑠𝑝2 hybrid orbitals are formed from two 𝑝-atomic orbitals and one 𝑠-orbital
c) 𝑑2 𝑠𝑝3 hydride orbitals are directed towards the corners of a regular octahedron
d) 𝑑𝑠𝑝 3hybrid orbitals are all at 90° to one another
368. Which statement is correct?
a) Pi-bond always exists with sigma-bond
b) Pi-bond can exist independently
c) Sigma-bond is weaker than pi-bond
d) Pi-bond is less reactive than sigma-bond
369. Which of the following pair has same structure?
a) PCl5 and SF6 b) SO2 and NH3 c) PH3 and BCl3 d) NH4+ and SO2−4
370. Which of the following has dipole moment?
a) CO2 b) p-dichlorobenzene c) NH3 d) CH4
371. Which one of the following is highest melting halide?
a) AgCl b) AgBr c) AgF d) AgI
372. The hybridisation state of central atom in PCl5 is
a) 𝑠𝑝3 𝑑 b) 𝑠𝑝 3 𝑑2 c) 𝑠𝑝3 d) 𝑑2 𝑠𝑝3
373. The correct order of increasing bond angles in the following triatomic species is:
a) NO− 2 < 𝑁O2 < 𝑁O2
+
b) NO+ 2 < 𝑁O2 < 𝑁O2
−
c) NO+ −
2 < 𝑁O2 < 𝑁O2 d) NO− +
2 < 𝑁O2 < 𝑁O2
374. K + , Cl− , Ca2+ , S2− ions are isoelectronic. The decreasing order of their size is:
a) S2− > 𝐶l− > K + > 𝐶a2+
b) Ca2+ > K + > 𝐶l− > S2−
c) K + > 𝐶l− > 𝐶a2+ > S2−
d) Cl− > S2− > 𝐶a2+ > K +
375. As the 𝑠-character of hybridization orbitals increases, the bond angle:
a) Increases b) Decreases c) Does not change d) Becomes zero
376. AlCl3 is covalent while AlF3 is ionic. This fact can be justified on the basis of
a) Valence bond theory b) Crystal structure c) Lattice energy d) Fajan rule
377. Which one of the following is a correct set with respect to molecule, hybridisation and shape?
a) BeCl2 , 𝑠𝑝2 , linear b) BeCl2 , 𝑠𝑝2 , triangular planar
c) BCl3 , 𝑠𝑝2 , triangular planar d) BCl3 , 𝑠𝑝3 , tetrahedral
378. In BrF3 molecule, the lone pairs occupy equatorial positions to minimize
a) Lone pair – bond pair repulsion only
b) Bond pair – bond pair repulsion only
c) Lone pair – lone pair repulsion and lone pair – bond pair repulsion
d) Lone pair – lone pair repulsion only
379. The correct order of decreasing polarity is
a) HF > 𝑆O2 > H2 O > 𝑁H3 b) HF > H2 O > 𝑆O2 > 𝑁H3
c) HF > 𝑁H3 > 𝑆O2 > H2 O d) H2 O > 𝑁H3 > 𝑆O2 > 𝐻F
380. The process requiring the absorption of energy is:
a) F − F − b) H → H − c) Cl → Cl− d) O → O2−
381. In O− 2−
2 , O2 and O2 molecular species, the total number of antibonding electrons respectively are
a) 7 , 6, 8 b) 1, 0, 2 c) 6, 6, 6 d) 8, 6, 8
382. 𝑠𝑝 hybridisation is found in
3
a) (I)> (II)> (IV) > (III) b) (I)> (III)> (II) > (IV)
c) (II)> (I)> (III) > (IV) d) (III)> (I)> (IV) > (II)
a) b) c) d)
a) CO2 b) SO2 c) N2 O d) CO
517. A 𝑠𝑝 -hybrid orbital contains:
3
a) b) c) d)
559. For the four successive transition elements (Cr, Mn, Fe and Co), the stability of +2 oxidation state will be
there in which of the following order?
a) Cr > 𝑀𝑛 > 𝐶𝑜 > 𝐹𝑒
b) Mn > 𝐹𝑒 > 𝐶𝑟 > 𝐶𝑜
c) Fe > 𝑀𝑛 > 𝐶𝑜 > 𝐶𝑟
Co > 𝑀𝑛 > 𝐹𝑒 > 𝐶𝑟
d)
(At. no. Cr = 24, Mn = 25, Fe = 26, Co = 27)
560. In PO3−
4 , the formal charge on each on each oxygen atom and the P − O bond order respectively are
a) −0.75, 0.6 b) −0.75, 1.0 c) −0.75, 1.25 d) −3, 1.25
561. An element X has 3 electrons in 𝑝-orbitals and also belongs to III period. Its molecular formula should be:
a) 𝑋 b) 𝑋2 c) 𝑋4 d) 𝑋5
562. Elements having six electrons in its outermost orbit generally form:
a) Complex ion b) Negative ion c) Positive ion d) Zwitter ion
563. Oxygen is divalent, but sulphur exhibits variable valency of 2, 4 and 6, because:
a) Sulphur is less electronegative than oxygen
b) Sulphur is bigger atom than oxygen
c) Ionisation potential of sulphur is more than oxygen
d) Of the presence of 𝑑-orbitals in sulphur
564. Of the following sets which one does not contain isoelectronic species?
a) BO3− 2−
3 , CO3 , NO3
−
b) SO2− 2− −
3 , CO3 , NO3 c) CN− , N2 , C22− d) PO3− 2− −
4 , SO4 , ClO4
565. In which of the following, unpaired electrons are present?
KO2 , AlO−2 , BaO2 , NO2
+
+
a) NO2 , BaO2 b) KO2 , AlO−
2 c) Only KO2 d) Only BaO2
566. Which transition involves maximum amount of energy?
a) 𝑀− (g) ⟶ 𝑀 (g) + e
b) 𝑀− (g) ⟶ 𝑀 + (g) + 2e
c) 𝑀+ (g) ⟶ 𝑀2+ (g) + e
d) 𝑀2+ (g) ⟶ 𝑀3+ (g) + e
567. What is the nature of the bond between B and O in(C2 H5 )2 OBH3?
a) Covalent b) Coordinate covalent
c) Ionic bond d) Banana shaped bond
568. Which does not use 𝑠𝑝 -hybrid orbitals in its bonding?
3
a) b) c) d)
a) b) c) d)
620. In the following electron-dot structure, calculate the formal charge from left to right nitrogen atom;
d) O− 2−
2 < 𝑁𝑂 < C2 < 𝐻e2
+
a) b) c) d)
a) b) c)
685. The relationship between the dissociation energy and N2 and N2+ is
a) dissociation energy of N2 = dissociation energy ofN2+
b) dissociation energy of N2 can either be lower or higher than the dissociation energy of N2+
c) dissociation energy of N2 > dissociation energy ofN2+
d) dissociation energy of N2+ > dissociation energy ofN2
686. The bond angle in H2 S (for H—S—H)is:
a) Same as that of Cl—Be—Cl in BeCl2
b) Greater thanH—N—H bond angle in NH3
c) Greater than H—Se—H and less than H—O—H
d) Same as Cl—Sn— Cl in SnCl2
687. Which one among the following does not have the hydrogen bond?
a) Phenol b) Water c) Liquid NH3 d) Liquid HCl
688. Which of the following molecules/ions does not contain unpaired electrons.
a) O2−2 b) B2 c) N2+ d) O2
689. The C − O − H bond angle in ethanol is nearly
a) 90 b) 104 c) 120 d) 180
690. Which one of the following does not have 𝑠𝑝 hybridised carbon?
2
a) NO2 and NH3 b) BF3 and NO− 2 c) NH2− and H2 O d) BF3 and NH2−
702. Bond length decreases with:
a) Decrease in size of the atom
b) Increase in the number of bonds between the atoms
c) Decrease in bond order
d) Decrease in the number of bonds between the atoms
703. Which of the following molecules/ ions does not contain unpaired electrons?
a) O2−2 b) B2 c) N2+ d) O2
704. The structure of IF7 is
a) Square pyramid b) Trigonalbipyramid
c) Octahedral d) Pentagonal bipyramid
705. The species C2
a) Has one 𝜎 bond and one 𝜋 bond b) Has both 𝜋 bonds
c) Has both 𝜎 bonds d) Does not exist
706. In which of the following bond angle is maximum?
a) NH3 b) NH4+ c) PCl5 d) SCl2
707. Oxidising power of chlorine in aqueous solution can be determined by the parameters indicated below
1
1 ∆ ∆ ∆
2 diss𝐻° EA 𝐻° hyd 𝐻°
Cl2 (g) → Cl(g) → Cl− (g) → Cl− (𝑎𝑞)
2
1
The energy involved in the conversion of Cl2 (g) to Cl− (𝑎𝑞)(Using the data)
2
−1
∆diss𝐻° Cl = 240 kJmol
2
b) O− 2−
2 < 𝑁𝑂 < C2 < 𝐻e2
+
767. Which one of the following compounds has bond angle as nearly 90°?
a) NH3 b) H2 S c) H2 O d) CH4
768. The hybrid state of sulphur in SO3 molecule is
a) 𝑠𝑝3 𝑑 b) 𝑠𝑝 3 c) 𝑠𝑝3 𝑑2 d) 𝑠𝑝2
769. In which of the following pair both molecules do not possess same type of hybridisation?
a) CH4 and H2 O b) PCl5 and SF4 c) SF6 and XeF4 d) BCl3 and NCl3
770. Which is the most covalent?
a) C − F b) C − O c) C − S d) C − Br
771. The shape of NO− 3 is planar. It is formed by the overlapping of oxygen orbitals with … orbitals of nitrogen.
a) 𝑠𝑝 -hybridized
3
b) 𝑠𝑝 -hybridized
2
c) Three 𝑝-orbitals d) None of these
772. Which of the ions has the largest ionic radius?
a) Be2+ b) Mg 2+ c) Ca2+ d) Sr 2+
773. A 𝜎-bonded molecule 𝑀𝑋3 is T-shaped. The number non-bonding pairs of electron is
a) 0
b) 2
c) 1
d) Can be predicted only if atomic number of M is known
774. Which of the following is not isoelectronic?
a) NO− b) CN− c) N2 d) O2+
2
775. In which set of molecules are all the species paramagnetic?
a) B2 , O2, N2 b) B2 , O2 , NO c) B2 , F2 , O2 d) B2 , O2 , Li2
776. Which of the following has strongest hydrogen bonding?
a) Ethylamine b) Ammonia c) Ethyl Alcohol d) Diethyl ether
777. The bonds present in N2 O5 are:
a) Ionic
b) Covalent and coordinate
c) Covalent
d) Ionic and covalent
778. The angle between two covalent bonds is maximum in:
a) CH4 b) H2 O c) CO2 d) SO3
779. The pair having similar geometry is
a) PCl3 , NH4 b) BeCl2 , H2 O c) CH4 , CCl4 d) IF5 , PF5
780. In the electronic structure of acetic acid there are:
a) 16 shared and 8 unshared valency electrons
b) 8 shared and 16 unshared valency electrons
c) 12 shared and 12 unshared valency electrons
d) 18 shared and 6 unshared valency electrons
781. Increasing order (lower first) of size of the various hybridised orbitals is:
a) 𝑠𝑝, 𝑠𝑝2 , 𝑠𝑝3 b) 𝑠𝑝 3 , 𝑠𝑝2 , 𝑠𝑝 c) 𝑠𝑝2 , 𝑠𝑝3 , 𝑠𝑝 d) 𝑠𝑝2 , 𝑠𝑝, 𝑠𝑝3
782. Among the following, the compound that contains ionic, covalent and coordinate linkage is
a) NH3 b) NH4 Cl c) NaCl d) CaO
783. How many bridging oxygen atoms are present in P4 O10 ?
a) 6 b) 4 c) 2 d) 5
784. Consider the Born-Haber cycle for the formation of an ionic compound given below and identify the
compound (Z) formed.
∆𝐻1 ∆𝐻2
𝑀(𝑠) → 𝑀(g) → 𝑀+ (g) ∆𝐻5
[1 ∆𝐻3 ∆𝐻4 ]→ 𝑍
𝑋2 (g) → 𝑋(g) → 𝑋 − (g)
2
a) 𝑀+ 𝑋 − b) 𝑀+ 𝑋 − (𝑠) c) 𝑀𝑋 d) 𝑀+ 𝑋 − (g)
785. The bond length is maximum in:
a) H2 S b) HF c) H2 O d) Ice
786. N2 andO2 are converted into monocations, N2+ and O+ 2 respectively. Which of the following is wrong?
+ +
a) In N2 , N − N bond weakens b) In O2 ,the O − O bond order increases
+
c) In O2 , paramagnetism decreases d) N2+ become diamagnetic
787. The number of nodal planes present in σ∗ s-antibondingorbitals is
a) 1 b) 2 c) 0 d) 3
788. Which of the following has maximum number of lone pairs associated with Xe?
a) XeO3 b) XeF4 c) XeF6 d) XeF2
789. Which is most volatile compound?
a) HI b) HCl c) HBr d) HF
−
790. The calculated bond order in O2 ion is
a) 1 b) 1.5 c) 2 d) 2.5
791. A C ≡ C bond is:
a) Weaker than C=C bond
b) Weaker than C—C bond
c) Longer than C—C bond
d) Shorter than C=C bond
792. In which of the following pairs bond angle is 109 ͦ28′ ?
a) [NH4+ ], [BF4− ] b) [NH4+ ], [BF3 ] c) [NH3 ], [BF4− ] d) [NH3 ], [BF3 ]
793. Which of the following molecules has three-fold axis of symmetry?
a) NH3 b) C2 H4 c) CO2 d) SO2
794. In which of the following arrangements the sequence is not strictly according to the property written
against it?
a) HF < 𝐻𝐶𝑙 < 𝐻𝐵𝑟 < 𝐻𝐼 : increasing acid strength
b) NH3 < 𝑃H3 < 𝐴𝑠H3 < 𝑆𝑏H3 : increasing basic strength
c) B < 𝐶 < 𝑂 < 𝑁 : increasing first ionization enthalpy
d) CO2 < 𝑆𝑖O2 < 𝑆𝑛O2 < 𝑃𝑏O2 :increasing oxidising power
795. Which one of the following is paramagnetic?
a) N2 b) NO c) CO d) O3
796. Which of the following has largest ionic radius?
a) Na+ b) K + c) Li+ d) Cs+
797. Lattice energy of a solid increases if
a) Size of ions is small b) Charges of ions are small
c) Ions are neutral d) None of the above
798. Which one is most polar?
a) CCl4 b) CHCl3 c) CH3 Cl d) CH3 OH
799. The high boiling point of water is due to:
a) Weak dissociation of water molecules
b) Hydrogen bonding among water molecules
c) Its high specific heat
d) Its high dielectric constant
800. The states of hybridisation of boron and oxygen atoms in boric acid ( H3 BO3 ) are respectively
a) 𝑠𝑝2 and 𝑠𝑝2 b) 𝑠𝑝 2 and 𝑠𝑝3 c) 𝑠𝑝3 and 𝑠𝑝2 d) 𝑠𝑝3 and 𝑠𝑝3
801. In which pair of species, both species do have the similar geometry?
a) CO2 , SO2 b) NH3 , BH3 c) CO2− 2−
3 , SO3 d) SO2− −
4 , ClO4
802. Which of the following is largest ion?
a) Na+ b) Mg 2+ c) O2− d) F −
803. The electronic configuration of sodium and chlorine justifies:
a) Their physical state
b) Their reactivity
c) The formation of electrovalent compound NaCl
d) None of the above
804. 𝑠𝑝3 hybridisation is found in
a) b) c) ClO−
3 d) SO3
805. Glycerol is more viscous than ethanol due to
a) High molecular weight b) High boiling point
c) Many hydrogen bonds per molecule d) Fajan’s rule
806. In the case of alkali metals, the covalent character decreases in the order:
a) MI > 𝑀𝐵𝑟 > 𝑀𝐶𝑙 > 𝑀𝐹
b) MCl > 𝑀𝐼 > 𝑀𝐵𝑟 > 𝑀𝐹
c) MF > 𝑀𝐶𝑙 > 𝑀𝐵𝑟 > 𝑀𝐼
d) MF > 𝑀𝐶𝑙 > 𝑀𝐼 > 𝑀𝐵𝑟
807. Two nodal planes are present in
a) b) σ2𝑝𝑧 c) π2𝑝𝑥 d) π2𝑝𝑦
808. H – bond is not present in
a) Water b) Glycerol
c) Hydrogen fluoride d) Hydrogen sulphide
809. In which of the following pairs molecules have bond order three and are isoelectronic?
a) CN− , CO b) CO, O+
2 c) NO+ , CO+ d) CN− , O+
2
810. Which of the following halides has maximum melting point?
a) NaF b) NaCl c) NaBr d) NaI
811. Which atomic orbital is always involved in sigma bonding only?
a) 𝑠 b) 𝑝 c) 𝑑 d) 𝑓
812. Which of the following acts sometimes as a metal and sometimes as a non-metal?
a) Hg b) Cl c) K d) At
813. Amongst the following elements the configuration having the highest ionization energy is:
a) [Ne]3𝑠 2 3𝑝1 b) [Ne]3𝑠 2 3𝑝3 c) [Ne]3𝑠 2 3𝑝2 d) [Ar]3𝑑10 4𝑠 2 4𝑝3
814. Which of the following species exhibits the diamagnetic behaviour ?
a) O2−
2 b) O+ 2 c) O2 d) NO
815. Which is a good solvent for ionic and polar covalent compounds?
a) H2 O b) CH3 COOH c) CCl4 d) Liquid NH3
816. The following salt shows maximum covalent character
a) AlCl3 b) MgCl2 c) CsCl d) LaCl3
817. Each of the followings has non-zero dipole moment, except:
a) C6 H6 b) CO c) SO2 d) NH3
818. Bonded electron pairs present in octahedral SF6 molecule:
a) 3 b) 4 c) 6 d) 5
819. Resonance structures can be written for
a) O3 b) NH3 c) CH4 d) H2 O
820. Born-Haber cycle may be used to calculate
a) Electronegativity b) Mass number c) Oxidation number d) Electron affinity
821. The electronic structure of four elements 𝐴, 𝐵, 𝐶, 𝐷 are
(𝐴)1𝑠 2 (𝐵)1𝑠 2 , 2𝑠 2 , 2𝑝 2
(𝐶)1𝑠 2 , 2𝑠 2 , 2𝑝5 (𝐷)1𝑠 2 , 2𝑠 2 , 2𝑝6
The tendency to form electrovalent bond is largest in
a) 𝐴 b) 𝐵 c) 𝐶 d) 𝐷
822. In which element shielding effect is not possible?
a) H b) Be c) B d) N
− + +
823. The hybridisation of orbitals of N atom in NO3 , NO2 and NH4 are respectively:
a) 𝑠𝑝, 𝑠𝑝2 , 𝑠𝑝3 b) 𝑠𝑝 2 , 𝑠𝑝, 𝑠𝑝3 c) 𝑠𝑝, 𝑠𝑝3 , 𝑠𝑝2 d) 𝑠𝑝2 , 𝑠𝑝3 , 𝑠𝑝
824. Which of the following is isoelectronic with carbon atom?
a) Na+ b) Al3+ c) O2− d) N +
825. Which of the following statement is correct?
a) Polarization of an anion is maximum by high charged cation
b) Small sized cation minimises the polarization
c) A small anion brings about a large degree of polarisation
d) A small anion undergoes a high degree of polarization
826. Among LiCl, BeCl2 , BCl3 and CCl4 , the covalent bond character follows the order:
a) LiCl > 𝐵𝑒𝐶l2 > 𝐵𝐶l3 > 𝐶𝐶l4
b) LiCl < 𝐵𝑒𝐶l2 < 𝐵𝐶l3 < 𝐶𝐶l4
c) LiCl > 𝐵𝑒𝐶l2 > 𝐶𝐶l4 > 𝐵𝐶l3
d) LiCl < 𝐵𝑒𝐶l2 < 𝐵𝐶l3 > 𝐶𝐶l4
827. The value of bond order in nitrogen and oxygen molecule is:
a) 3, 2 b) 4, 2 c) 2, 3 d) 1, 2
828. Pauling received Nobel Prize for his work on:
a) Photosynthesis b) Atomic structure c) Chemical bonding d) Thermodynamics
829. With which of the given pairs CO2 resembles?
a) HgCl2 , C2 H2 b) C2 H2 , NO2 c) HgCl2 , SnCl4 d) N2 O, NO2
830. The enhanced force of cohesion in metals is due to:
a) The covalent linkages between atoms
b) The electrovalent linkages between atoms
c) The lack of exchange of valency electrons
d) The exchange energy of mobile electrons
831. Among H𝑋, the maximum dipole moment is of:
a) HF b) HCl c) HBr d) HI
832. Dative bond is present in:
a) SO3 b) NH3 c) BaCl2 d) BF3
833. In which of the following molecule, the central atom does not have 𝑠𝑝3 -hybridization?
a) CH4 b) SF4 c) BF4− d) NH4+
834. Which has an odd electron and shows paramagnetic character?
a) NO b) SO2 c) CO2 d) H2 O
835. Which ion is not isoelectronic with O2− ?
a) N3− b) Na+ c) F − d) Ti+
836. Which species is paramagnetic?
a) O−
2 b) CH3− c) CO d) NO+
837. Structure of ammonia is
a) Pyramidal b) Tetrahedral c) Trigonal d) Trigonal pyramidal
838. The example of the p-p-orbital overlapping is the formation of:
a) H2 molecule
b) Cl2 molecule
c) Hydrogen chloride
d) Hydrogen bromide molecule
839. In which of the following 𝑝𝜋 - 𝑑𝜋 bonding is observed?
a) NO−3 b) SO2−
3 c) BO3−3 d) CO2−
3
840. The shape of ClO− 4 ion is:
a) Square planar b) Square pyramidal c) Tetrahedral d) Trigonal bipyramidal
841. The critical temperature of water is higher than that of O2 because H2 O molecule has:
a) Fewer electrons than O2
b) Two covalent bonds
c) V-shape
d) Dipole moment
842. Compound formed by 𝑠𝑝3 𝑑-hybridization will have structure:
a) Trigonal bipyramidal
b) T-shaped
c) Linear
d) Either of these depending on number of lone pair of electrons of central atom
843. Which has the lowest bond angle?
a) NH3 b) BeF2 c) H3 O+ d) CH4
844. Assuming that Hund’s rule is violated, the bond order and magnetic nature of the diatomic molecule B2 is
a) 1 and diamagnetic
b) 0 and diamagnetic
c) 1 and paramagnetic
d) 0 and paramagnetic
845. The energy of antibonding molecular orbitals is:
a) Greater than the bonding M.O.
b) Smaller than the bonding M.O.
c) Equal to that of bonding M.O.
d) None of the above
846. The set representing the correct order of ionic radius is:
a) Na+ > 𝐿i+ > 𝑀g 2+ > 𝐵e2+
b) Li+ > 𝑁a+ > 𝑀g 2+ > 𝐵e2+
c) Mg 2+ > 𝐵e2+ > 𝐿i+ > 𝑁a+
d) Li+ > 𝐵e2+ > 𝑁a+ > 𝑀g 2+
847. Which of the following hydrogen bonds is the strongest?
a) b) c) d)
848. H2 Ois dipolar, whereas BeF2 is not. It is because
a) The electronegativity of F is greater than that of O
b) H2 O involves hydrogen bonding whereas BeF2 is a discrete molecule
c) H2 O is linear and BeF2 is angular
d) H2 O is angular and BeF2 is linear
849. Which of the following statements is most correct? Effective nuclear charge of an atom depends on:
a) The atomic number of the atom
b) The charge on the ion
c) The shielding effect
d) Both the actual nuclear charge and the shielding effect
850. The total number of valency electrons in PH4+ ion is:
a) 8 b) 9 c) 6 d) 14
851. Phosphoric acid is syrupy in nature due to
a) Strong covalent bonding b) Hydrogen bonding
c) van der Waals’ forces d) None of the above
852. The correct order of bond angles is:
a) H2 S < 𝑁H3 < 𝐵F3 < 𝑆𝑖H4
b) NH3 < H2 S < 𝑆𝑖H4 < 𝐵F3
c) H2 S < 𝑁H3 < 𝑆𝑖H4 < 𝐵F3
d) H2 S < 𝑆𝑖H4 < 𝑁H3 < 𝐵F3
853. Metallic lusture is explained by
a) Diffusion of metal ions b) Oscillation of loose electrons
c) Excitation of free protons d) Existence of bcc lattice
854. Which of the following phenomenon will occur when two atoms of same spin will react?
a) Bonding will not occur
b) Orbital overlap will not occur
c) Both (a) and (b)
d) None of the above
855. The hybrid state of S in SO3 is similar to that of
a) C in C2 H2 b) C in C2 H4 c) C in CH4 d) C in CO2
856. Among the following the pair in which the two species are not isostructural is
a) IO−3 and XeO3 b) PF6− and SF6 c) BH4− andNH4+ d) SiF4and SF4
857. Which of the following species contains three bond pairs and one lone pair around the central atom?
a) NH2− b) PCl3 c) H2 O d) BF3
858. Intramolecular hydrogen bonding is found in:
a) Salicyldehyde b) Water c) Acetaldehyde d) Phenol
+
+
859. The type of bond formed between H and NH3 in NH4 ion is:
a) Ionic b) Covalent c) Dative d) Hydrogen
860. Which of the following statements is correct about N2 molecule?
a) It has a bond order of 3 b) The number of unpaired electrons present in it is
zero and hence, it is diamagnetic
The order of filling of MOs is 𝜋(2𝑝𝑥 ) = d) All the above three statements are correct
c)
𝜋(2𝑝𝑦 ), 𝜎(2𝑝𝓏 )
861. Ice has an open structure compared to water due to which it floats on water and occupies a greater volume
of space. The open structure of ice is due to:
a) Solid state of ice b) Its low density c) Crystalline nature d) Hydrogen bonding
862. Which of the following has minimum melting point?
a) CsF b) HCl c) HF d) LiF
863. Geometry of ammonia molecule and the hybridisation of nitrogen involved in it are
a) 𝑠𝑝3 hyridisation and tetrahedral geometry
b) 𝑠𝑝3 hyridisation and distorted tetrahedral geometry
c) 𝑠𝑝2 hyridisation and triangular geometry
d) None of the above
864. The molecule having smallest bond angle is
a) H2 O b) H2 S c) NH3 d) H2 Te
865. For a covalent solid, the units which occupy lattice points are:
a) Atoms b) Ions c) Molecules d) Electrons
866. Carbon suboxide (C3 O2 ) has recently been shown as a component of the atmosphere of Venus. Which of
the following formulation raepresents the correct ground state Lewis structure for carbon suboxide?
a) :O:C::C:C:O: b) :O::C::C:C::O: c) : Ö::C::C::C:: Ö: d) :O: C: C: C: O:
867. The ionization energy will be maximum for the process:
a) Ba ⟶ Ba2+ b) Be ⟶ Be2+ c) Cs ⟶ Cs+ d) Li ⟶ Li+
868. Born Haber cycle is used to determine:
a) Lattice energy b) Electron affinity c) Ionization energy d) Either of them
869. In which of the following molecules/ions BF3 , NO− 2 , NH −
2 , and H 2 O the central atom is 𝑠𝑝2 hybridized?
a) BF3 and NO− 2 b) NO− 2 and NH2
−
c) NH2− and H2 O d) NO− 2 and H2 O
870. 𝑠𝑝 𝑑 hybridisation results in
3
The anion ‘X ’ is
a) N2− b) O−2 c) N22− d) O2−
2
885. According to Fajan’s rule polarization is more when:
a) Small cation and large anion
b) Small cation and small anion
c) Large cation and large anion
d) Large cation and small anion
886. Organic compounds soluble in water contain:
a) C, H. Cl b) C, H c) C, H, O d) C, S
887. Atomic radii of fluorine and neon in angstrom unit are respectively given by:
a) 0.72, 1.60 b) 1.60, 1.60 c) 0.72, 0.72 d) 1.60, 0.72
888. The decreasing order of bond angle is
a) NO2 > NO+ 2 > NO2
−
b) NO− +
2 > 𝑁O2 > NO2
+ − + −
c) NO2 > 𝑁O2 > NO2 d) NO2 > NO2 > 𝑁O2
889. The correct order of dipole moment is:
a) CH4 < 𝑁F3 < 𝑁H3 < H2 O
b) NF3 < 𝐶H4 < 𝑁H3 < H2 O
c) NH3 < 𝑁F3 < 𝐶H4 < H2 O
d) H2 O < 𝑁H3 < 𝑁F3 < 𝐶H4
890. Which oxide of nitrogen is isoelectronic with CO2 ?
a) NO2 b) N2 O c) NO d) N2 O2
891. Which of the following molecules does not possess a permanent electric dipole moment?
a) H2 S
b) SO2
c) SO3
d) CS2
892. Among O, C, F, Cl, Br the correct order of increasing atomic radii is:
a) F < 𝑂 < 𝐶 < 𝐶𝑙 < 𝐵𝑟 b) F < 𝐶 < 𝑂 < 𝐵𝑟 < 𝐶𝑙 c) F < 𝐶𝑙 < 𝐵𝑟 < 𝑂 < 𝐶 d) C < 𝑂 < 𝐹 < 𝐶𝑙 < 𝐵𝑟
893. In which of the following diatomic molecules /ions is the bond order of each molecule/ion = 2.5?
a) O+2 , NO, CN
−
b) CN− , N2+ , N2 c) N2+ , NO, O+
2 d) O+ − +
2 , CN , N2
894. What type of hybridisation takes place in the N atom ofNH3 ?
a) 𝑠𝑝2 b) 𝑠𝑝 3 c) 𝑑𝑠𝑝2 d) 𝑠𝑝
895. Identify the correct order of solubility of Na2 S, CuS and ZnS in aqueous medium:
a) CuS > 𝑍𝑛𝑆 > 𝑁a2 S b) ZnS > 𝑁a2 S > 𝐶𝑢𝑆 c) Na2 S > 𝐶𝑢𝑆 > 𝑍𝑛𝑆 d) Na2 S > 𝑍𝑛𝑆 > 𝐶𝑢𝑆
896. In the following molecule, the two carbon atoms marked by asterisk (*) possess the following type of
hybridized orbitals:
a) Atomic number
b) Atomic mass
c) Equivalent weight
d) Number of valency electrons
904. In the following, which bond will be responsible for maximum value of hydrogen bond?
a) N − H b) O − H c) F − H d) S − H
+
905. The bond order of O2 is the same as in
a) N2+ b) CN− c) CO d) NO+
+
906. Structure of XeF5 ion is
a) Trigonalbipyramidal b) Square pyramidal c) Octahedral d) Pentagonal
907. The fHOMO in CO is
a) 𝜋- bonding b) 𝜋-antibonding c) 𝜎-antibonding d) 𝜎- bonding
908. Which of the following has 𝑠𝑝3 -hybridization on central atom?
a) BF2 b) BCl3 c) SO3 d) CCl4
909. Which one has 𝑠𝑝 hybridisation?
3
a) N2 O b) CO2 c) SO2 d) CO
910. Coordinate compounds are formed by:
a) Transfer of electrons
b) Sharing of electrons
c) Donation of electron pair
d) None of the above
911. In P4 O10 the
a) Second bond in P = O is formed by 𝑝𝜋 − 𝑑𝜋 back bonding
b) P = O bond is formed by pπ − pπ bonding
c) P = O bond is formed by dπ − dπ bonding
d) P = O bond is formed by dπ − dπ − 3σ back bonding
912. Allene(C3 H4 ) contains
a) One double bond, one triple bond and one single bond
b) One triple and two double bonds
c) Two triple and one double bond
d) Two double and four single bond
913. Which shows non-directional bonding?
a) BCl3 b) CsCl c) NCl3 d) BeCl3
914. Which one of the following contains both ionic and covalent bonds?
a) C6 H5 Cl b) H2 O c) NaOH d) CO2
915. Na , Mg , Al , Si areisoelectronics. Their ionic size follows the order:
+ 2+ 3+ 4+
a)
b)
c)
d)
934. Which one pair of atoms or ions will have same configuration?
a) Li+ and He− b) Cl− and Ar c) Na and K d) F + and Ne
935. Which combination is best explained by the coordinate covalent bond?
1
a) H + + H2 O b) Cl + Cl c) Mg + O2 d) H2 + I2
2
936. The dipole moment of CHCl3 is 1.05 debye while that of CCl4 is zero, because CCl4 is:
a) Linear b) Symmetrical c) Planar d) Regular tetrahedral
937. Which shows the highest lattice energy?
a) RbF b) CsF c) NaF d) KF
938. In a polar molecule, the ionic charge is 4.8 × 10 −10
e.s.u. If the inter ionic distance is 1 Å unit, then the
dipole moment is
a) 41.8 debye b) 4.18 debye c) 4.8 debye d) 0.48 debye
939. The correct order regarding the electronegativity of hybrid orbitals of carbon is:
a) 𝑠𝑝 < 𝑠𝑝2 > 𝑠𝑝3 b) 𝑠𝑝 < 𝑠𝑝2 < 𝑠𝑝3 c) 𝑠𝑝 > 𝑠𝑝2 < 𝑠𝑝 3 d) 𝑠𝑝 > 𝑠𝑝2 > 𝑠𝑝3
940. Which of the following groups all do not have 𝑠𝑝3 𝑑 hybridisation?
a) ClF3 , IF3 , XeF3+ b) ICl− − −
2 , ClF2 , I3 c) ClF3 , BrF3 , IF3 d) PCl3 , AsCl3 , PF5
941. Which of the following compounds does not follow the octet rule for electron distribution?
a) H2 O b) PH3 c) PCl3 d) PCl5
942. Which of the following sets represents the collection of isoelectronic species?
a) Na+ , Mg 2+ , Al3+ , Cl− b) Na+ , Ca2+ , Sc 3+ , F − c) K + , Cl− , Mg 2+ , Sc 3+ d) K + , Ca2+ , Sc 3+ , Cl−
943. Which of the following has unchanged valency?
a) H b) Na c) Fe d) O
944. The structure of XeF4 is:
a) Planar b) Tetrahedral c) Square planar d) Pyramidal
+ +
945. N2 and O2 are converted into N2 and O2 respectively.
Which of the following is not correct?
a) In N2+ , the N – N bond weakens
b) In O+
2 , O – O bond order increases
c) In O+
2 , paramagnetism decreases
+
d) N2 becomes diamagnetic
946. Which molecule has trigonal planar geometry?
a) IF3 b) PCl3 c) NH3 d) BF3
947. Malleability and ductility of metals can be accounted due to
a) The presence of electrostatic force
b) The crystalline structure in metal
c) The capacity of layers of metal ions to slide over the other
d) The interaction of electrons with metal ions in the lattice
948. Underlined carbon is 𝑠𝑝3 hybridised in
a) CH3 CH = CH2 b) CH3 CH2 NH2 c) CH3 CONH2 d) CH3 CH2 CN
949. Hydrogen fluoride is a liquid unlike other hydrogen halides because:
a) HF molecules associate due to hydrogen bonding
b) F2 is highly reactive
c) HF is the weakest acid of all hydrogen halides
d) Fluorine atom is the smallest of all halogens
950. The number of sigma (𝜎)and pi (𝜋) covalent bonds respectively in banzenenitrile are
a) 5, 13 b) 15, 3 c) 13, 5 d) 16, 2
951. In which one of the following cases, breaking of covalent bond takes place?
a) Boiling of H2 O b) Melting of KCN c) Boiling of CF4 d) Melting of SiO2
952. Which compound is soluble in water
a) CS2 b) C2 H5 OH c) CCl4 d) CHCl3
953. A π-bond is formed by sideways overlapping of:
a) 𝑠-𝑠 orbitals b) 𝑝-𝑝 orbitals c) 𝑠-𝑝 orbitals d) 𝑠-𝑝-𝑠 orbitals
954. Which statement is true?
a) Absolutely pure water does not contain any ion.
b) Some covalent compounds may also give ions in aqueous solution.
c) In aqueous solution only electrovalent compound give ions.
d) Very sparingly soluble substances do not dissociate in aqueous solution
955. Formation of π-bond:
a) Increases bond length
b) Decreases bond length
c) Distorts the geometry of molecule
d) Makes homoatomic molecules more reactive
956. In which reaction, the hybridisation on the central atom changes from 𝑠𝑝2 to 𝑠𝑝3 ?
a) NH3 + H + ⟶ NH4+ b) BF3 + F − ⟶ BF4− c) H2 0 + H + ⟶ H3 O+ d) C2 H2 + 2H2 ⟶ C2 H6
957. The low solubility of BaSO4 in water is due to:
a) Low dissociation energy
b) Ionic bonds
c) High value of lattice energy
d) None of the above
958. The number of lone pairs of electron on Xe in XeOF4 is:
a) 1 b) 2 c) 3 d) 4
959. Which compound does not contain double bond or triple bond?
a) C2 H4 b) H2 O c) N2 d) HCN
960. The compound showing maximum covalent character is:
a) BI3 b) BCl3 c) BF3 d) BBr3
961. Carbon atoms in C2 CN 4 are:
( )
a) 𝑠𝑝-hybridised
b) 𝑠𝑝2 -hybridised
c) 𝑠𝑝- and 𝑠𝑝2 -hybridised
d) 𝑠𝑝, 𝑠𝑝2 and 𝑠𝑝3 -hybridised
962. Which statement is wrong?
a) 2nd ionisation energy shows jump in alkali metals
b) 2nd electron affinity for halogens is zero
c) Maximum electron affinity exists for F
d) Maximum ionization energy exists for He
963. Value of 𝑥 in potash alum,
K 2 SO4 . AI𝑥 (SO4 )3 . 24H2 O is
a) 4 b) 1 c) 2 d) None of these
964. Among the following, the paramagnetic compound is
a) Na2 O2 b) O3 c) N2 O d) KO2
965. HCl molecule in the vapour state is an example of:
a) Non-polar bond b) Ionic bond c) Polar covalent bond d) Pure covalent bond
966. The electrons in an incomplete outershell are known as:
a) Kernel electrons b) Valency electrons c) Shell electrons d) None of the above
967. According to bond order concept the correct order of stability of O2 , O+2 , and O−
2 is
a) O2 > O+ 2 > O −
2 b) O −
2 > O 2 > O+
2 c) O 2 > O −
2 > O +
2 d) O+2 > O2 > O2
−
968. The element which exists in both hard and soft form is:
a) Fe b) Si c) C d) Al
969. Which of the following is not a correct statement?
a) Every AB5 molecule does in fact have square pyramid structure.
b) Multiple bonds are always shorter than corresponding single bonds.
c) The electron-deficient molecules can act as Lewis acids.
d) The canonical structures have no real existence.
970. The bond strength increases:
a) With increasing bond order
b) With increasing extent of overlapping of orbitals
c) With decreasing difference between energies of overlapping orbitals
d) All of the above
971. The number of unpaired electrons in O2 molecule is:
a) Zero b) 1 c) 2 d) 3
972. Which has higher bond energy and stronger bond?
a) F2 b) Cl2 c) Br2 d) I2
973. Which of the following statements regarding carbon monoxide is correct?
a) It involves 𝑠𝑝-orbitals of carbon
b) It contains a lone pair only on carbon
c) It contains a lone pair only on oxygen
d) In carbonyl, oxygen end is attached to the metal atoms
974. Which of the following is having highest bond length?
a) NO− b) NO+ c) CN− d) CN+
975. Which of the following statement is correct for CsBr3 ?
a) It is a covalent compound
b) It contains Cs3+ and Br − ions
c) It contains Cs+ and Br3− ions
d) It contains Cs+ , Br − and lattice Br2 molecule
976. In 1 – butene number of σ - bonds is
a) 8 b) 10 c) 11 d) 12
977. Which does not have pyramidal geometry?
a) SO2−3 b) NO− 3 c) NH3 d) C(C6 H5 )−
3
978. The nature of bonding in CCl4 and CaH2 :
a) Electrovalent in both CCl4 and CaH2
b) Covalent in CCl4 and electrovalent in CaH2
c) Electrovalent in CCl4 and covalent in CaH2
d) None of the above
979. Which of the following oxides is not expected to react with sodium hydroxide?
a) BeO b) B2 O3 c) CaO d) SiO2
1 (b) μcal = 2.0 × 10−10 m × 1.6 × 10−19 C
Molecule Hybridizatio = 3.2 × 10−29 C − m.
n μexp
Percentage of ionic character = × 100
SO3 𝑠𝑝2 μcal
C2 H2 𝑠𝑝 5.12 × 10−29
= × 100 = 16%
C2 H4 𝑠𝑝2 3.2 × 10−29
CH4 𝑠𝑝3 11 (c)
CO2 𝑠𝑝 C2 H4involves𝑠𝑝2 -hybridization on carbon atoms.
2 (b) 12 (b)
Mg 2+ is smaller thanNa+ and thus, smaller is According to molecular orbital theory.
cation more is hydration energy. F2 (18) = 𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜎2𝑝𝑧2 , 𝜋2𝑝𝑥2
3 (b) ≈ 𝜋2𝑝𝑦2 ,∗𝜋 2𝑝𝑥,
2
≈ ∗𝜋 2𝑝𝑦2
Number of lone pair in XeOF4 is one (1). The 𝑁 𝑁 10−8
Bond order in F2 = 𝑏−2 𝑎 = 2 = 1
structure of XeOF4 is given as follows :
15 (a)
Bond formation is always exothermic. Compounds
of sodium are ionic.
16 (d)
In case of water, five water molecules are
attached together through four hydrogen bonding
17 (b)
Removal of electron is easier in the order of shell
4>3>2>1
18 (c)
Bond order of NO+ , NO and NO− are 3, 2.5 and 2
respectively.
Bond energy ∝ bond order.
19 (a)
FXF angles of two types are present in 𝑠𝑝3 𝑑
One π-bond so remaining six electron pairs form hybrid orbitals. Since, SF4 shows 𝑠𝑝3 𝑑
an octahedron with one position occupied by a hybridisation as follows, therefore, it exhibits two
lone pair. different FXF angles.
4 (d)
These are the factors on which van der Waals’
forces depend.
5 (b)
It has 𝑠𝑝3 𝑑3 -hybridization with one lone pair on
X𝑒. 20 (c)
6 (b) 𝑠-character ∝ bond angle
1
Bond order ∝ Bond length For 25% 𝑠 character (as in 𝑠𝑝3 hybrid orbital),
bond angle is 109.5°, for 33.3% 𝑠 character (as in
BO of NO<BO of NO+
𝑠𝑝2 hybrid orbital),bond angle is 120° and for
∴ Bond length of NO is greater than the bond
50% 𝑠 character (as in 𝑠𝑝 hybrid orbital ), bond
length of NO+ .
angle is 180°.
7 (b)
Similarly, when the bond angle decreases below
Element with atomic number 20 is metal (Ca); it
1.9.5°,the𝑠 −character will decrease accordingly
will combine with non-metal.
Decreasing in angle = 120° − 109.5° = 10.5°
8 (a)
∴ Decrease in 𝑠-character = 33.3 − 25 = 8.3
A decrease in 𝑠-character increases bond length.
Actual decrease in bond angle = 109.5° − 105° =
10 (b)
4.5°
Calculated dipole moment,
∴ Expected decrease in 𝑠-character
8.3 29 (c)
= × 4.5 = 3.56%
10.5 Alleneis CH2 = C = CH2 .
Thus, the 𝑠-character should decrease by about 30 (a)
3.56%, 𝑖𝑒, 𝑠-character = 25 − 3.56 = 21.44% Silicate ion (Sio4−4 ) is the basic structural unit of
21 (b) silicates. Silicates are metal derivatives of silicic
B has only six electron in B2 H6 . acid.
22 (a) 31 (a)
Like gets dissolved in like. It is theory. Due to planar equilateral geometry of graphite.
23 (c) 32 (a)
Ionic compounds are good conductor of electricity Due to non-availability of 𝑑-orbitals, boron cannot
in molten or in solution state. However, they are expand its octet. Therefore, the maximum
bad-conductor in solid state. covalence of boron cannot exceed 4.
24 (d) 33 (b)
In benzene 12σ and 3πbonds are present. The Cations are always shorter than their parent
structure of benzene is atom, anion are always larger.
35 (a)
H-bonding is weakest bonding.
36 (a)
5 of P + 24 of O + 3 of –ve charge = 32.
37 (c)
Benzene has 12σ-and 3π-bonds.
38 (c)
PF5 involves𝑠𝑝3 𝑑-hybridization.
39 (b)
I3− ion is made up of an I2 molecule with an I −
25 (c)
bonded to it by means of a coordinate bond in
In CO2− ion the C-atom undergoes𝑠𝑝2 -
3 which I2 is lone pair acceptor (Lewis acid) and I −
hybridisation. It has triangular planar structure.
the lone pair donor (Lewis base). There are two
While BF4− , NH4+ andSO2−
4 have tetrahedral
bond pairs and three lone pairs in the outer shell
structure.
of central atom. To minimize the repulsive forces
26 (d)
the three lone pairs occupy the equatorial
PCl5 has trigonal bipyramid geometry.
position. The ion is therefore, linear in shape with
27 (b)
a bond angle of exactly180°.
SF6 has octahedral geometry, 𝑠𝑝3 𝑑2 hybridisation I
and bond angle is 90°
2 (no.of 𝑑−orbitals)
% of d-character = 6(total hybridised orbitals) ×
100 Similarly, N3− ion is also linear in shape.
= 33% 40 (c)
So, SF6 are bond angle = 90° According to M.O. theory, bond order of
andd-character = 33%. N2 , N2− and N22− are 3, 2.5 and 2 respectively.
28 (a) 41 (b)
Head on overlapping give rise to σ-bond 𝑒.g., BF3 .
formation.
42 (d) Follow Fajans’ rule.
Bond order for H2− = +1/2 58 (b)
43 (b) Removal of two electrons (one by one) from an
𝑠𝑝-hybridization leads to bond angle of 180 ͦ. atom requires energy = IP1 + IP2 .
44 (c) 59 (c)
μ H2 O ≠ 0, μCO2 = 0 The molecular orbital electronic configuration.
∗ ∗
45 (b) (𝜎1𝑠)2 (𝜎 1𝑠)2 (𝜎2𝑠)2 (𝜎 2𝑠)2 (𝜎2𝑝𝑥 )2
1 ∗ ∗
No, of hybrid orbital = 2 [No.of𝑒 − inV-shell of 2 2 (𝜋2𝑝𝑧 )1
(𝜋2𝑝𝑦 ) (𝜋2𝑝𝑧 )2 (𝜋2𝑝𝑦 )
atom + No.of monovalent atoms –charge on Total electrons =17
cation +charge on anion] Hence, this configuration belongs to O− −
2 (17𝑒 )
No. of hybrid orbital 2 3 4 5 ion.
6 7 60 (a)
Type of hybridisation𝑠𝑝𝑠𝑝2 𝑠𝑝3 𝑠𝑝3 𝑑𝑠𝑝3 𝑑2 𝑠𝑝3 𝑑3 H3 O+ ∶ 𝑠𝑝3 ; NO− 2
3 ∶ 𝑠𝑝
Hybridisation in TeCl4 : 61 (a)
1
No. of hybrid orbital = 2 [6 + 4 + 0 + 0] = 5 6, 6
3
Hence, TeCl4 shows 𝑠𝑝 𝑑 hybridisation. 62 (a)
46 (a) More is the dipole moment more is ionic nature.
The stability and bond angle order for hybrids in a μ = δ × d; higher is μ, more will be δ on the atom.
group is NH3 > 𝑃H3 > 𝐴𝑠H3 > 𝑆𝑏H3 > 𝐵𝑖H3 . 63 (c)
47 (c) Due to 𝑠𝑝3 -hybridization.
Isoelectronic species are those species which have 65 (a)
equal number of electrons. Hence, CO2 is Each species has 14 electrons and bond order for
isoelectronic with N2 O. each is three.
Number of electron in CO2 =22 66 (a)
Number of electron in N2 O=22 Among the given choices of compound having
48 (d) oxygen attached to hydrogen will have maximum
In BeCl2 , Be atom has incomplete octet. hydrogen bonding.
49 (a) ∵ Among CH3 OCH3, (CH3 )2 C = O, CH3 CHO and
Greater the charge, smaller the radius, greater the C2 H5 OH only C2 H5 OH has oxygen attached to
polarising power and thus greater the covalent hydrogen atom.
nature. This leads to increase in lattice energy. ∴ C2 H5 OHshows maximum hydrogen bonding.
50 (c) 67 (c)
The structure,CH2 = C = CH2 is non-planar with It is experimental value.
two – CH2 groups being in planes perpendicular 68 (c)
to each other. O2+
2 has 14 electrons. Its electronic configuration
52 (d) is as
+
Electronegativity increases along the period and O2 ∶ 𝜎1𝑠 2 ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 ∗𝜎 2𝑠 2 , 𝜋2𝑝𝑦2 𝜋2𝑝𝑧2 𝜎2𝑝𝑥2
decreases down the group. 𝑁 𝑁 10−4
Bond order = 𝑏−2 𝑎 = 2 = 3
53 (a)
69 (c)
Brass in an alloy.
In diamagnetic molecule, all the electrons are
54 (c)
paired
It is head on overlapping and thus, forms more
70 (a)
stronger bond.
55 (c)
H-bonding in molecule gives rise to increase in its
b.p.
56 (b)
One bonding molecular orbital and one
antibonding.
57 (a)
78 (c)
N2 Ois isoelectronic with CO2 and N3− .
Hence, its structure is linear.
N−N−O
79 (d)
H atom attached on N, O, F develops hydrogen
bonding molecule.
80 (d)
In CCl4 all bonds of carbon being identical, the
molecule is a regular tetrahedron
81 (c)
Hence, enolic form of acetone contains 9 sigma
In O2− effective nuclear charge is minimum due to
bonds, 1 pi bond and two lone pairs.
more number of electrons and thus the size of O2−
71 (a)
is maximum.
In NO− 3 ion, total number of electrons =
82 (b)
7+24+1=32 and in it central atom is 𝑠𝑝2 hybrid.
𝑉−8𝐵 24−8×3 The zero dipole moment of BF3 molecule is due to
No. of hybrid orbitals = 2 + 𝐵 = 2
+ 3 its symmetrical (triangular planar) structure.
(𝑉 → total number of electrons in valence shell
𝐵 → probability of formation of bond)
In CO2−3 ion, total number of electrons =
6+24+2=32 and in it central atom is 𝑠𝑝2 hybrid.
24−8×3
No. of hybrid orbital= 2
+3=3 84 (b)
Hence, NO−
3 and 2−
CO3 ions are isoelectronic and Bond dissociation energy order:
isostructural. Cl2 > 𝐵r2 > F2 > I2
72 (b) 242.6 192.8 158.8 151.1 in kJ mol−1
H2+ = 𝜎1𝑠 2 (According to molecular orbital 85 (b)
theory) CH3 OHshows H—bonding in liquid state.
Bond order =
bonding electrons−antibonding electrons 86 (b)
2
They have high electron density.
1
= = 0.5 87 (c)
2
H2+ is paramagnetic due to the presence of one A coordinate bond is a dative covalent bond in
unpaired electron. which two atoms form bond and one of them
73 (b) provides both electrons.
H-bonding in molecules gives rise to increase in 𝑋: +𝑌 ⟶ 𝑋: 𝑌or 𝑋 ⟶ 𝑌
b.p. 88 (b)
74 (a) C − Cbond length in 𝑠𝑝2 hybrid molecule is=
Bond distance is in the order : 1.39Å
C−C>𝐶 =𝐶 >𝐶 ≡𝐶 89 (d)
𝑠𝑝3 > 𝑠𝑝2 > 𝑠𝑝 More is electronegativity differences, more is
75 (a) ionic character.
% ionic character = 16(𝑥𝐴 − 𝑥𝐵 ) + 3.5(𝑥𝐴 − 𝑥𝐵 ) 2 90 (a)
= 16 × 2 + 3.5 × (22 ) Cation are always smaller than their parent
= 46 atoms:
∴ The % covalent character = 100 − 46 = 54 Al3+ < 𝐴l2+ < 𝐴l+ < 𝐴𝑙.
76 (d) 91 (a)
ICl− 3 We know that the C − C bond length = 1.54 A, C
2 has𝑠𝑝 𝑑-hybridized state (𝑖. 𝑒., trigonal
bipyramidal shape but distorted due to the =C bond length = 1.34 A and C ≡ C bond length
presence of lone pair of electron on I atom.) = 1.20 A. Since propyne has triple bond;
77 (a) therefore, it has minimum bond length.
Like gets dissolved in like. 92 (c)
Ionic compounds conduct current in molten state. molecular orbital.
93 (d) 104 (d)
Metals are good conductor of electricity because PCl3 < 𝑃𝐵r3 < 𝑃I3 , the bond angle order is
they contain free electrons. explained in terms of increasing electronegativity
94 (d) of halogens, whereas, PF3 > 𝑃𝐶l3 , bond angle
OSF2 has pyramidal shape order is explained in terms of pπ - dπ bonding in
PF3 .
105 (c)
μ experimental = Dipole moment × 10−18
μ theoretical = Bond length × 4.8 × 10−10 esu
× cm
μexperimental
95 (d) Percentage ionic character = × 100
μtheoretical
Non-polar species exert van der Waals’ forces
among themselves.
96 (b)
1.0 × 10−18 × 100
It has 3σ-and 1π-bond. =
97 (c) 1.25 × 4.8 × 10−10 × 10−8
= 16.66%
Cl− has1𝑠 2 , 2𝑠 2 2𝑝6 , 3𝑠 2 3𝑝6 configuration.
106 (d)
98 (c)
CCl4does not exhibit dipole moment due to its
Per cent ionic character is given by % of ionic
symmetrical structure.
character.
Cl
= 16(𝑋𝐴 − 𝑋𝐵 ) + 3.5(𝑋𝐴 − 𝑋𝐵 )2
|
From the above relation, it is clear that as soon as
Cl − C − Cl
(𝑋𝐴 − 𝑋𝐵 )increases, % ionic character will also
|
increase.
Cl
Therefore, curve C shows a correct path.
107 (a)
99 (d)
N2 molecule has 14 electrons. The molecular
7Cl=1𝑠 2 , 2𝑠 2 , 2𝑝6 , 3𝑠 2 , 3𝑝𝑥2 , 3𝑝𝑦2 , 3𝑝𝑧1
orbital electronic configuration of the molecule is
Cl=1𝑠 2 , 2𝑠 2 , 2𝑝6 , 3𝑠1 , 3𝑝𝑥1 , 3𝑝𝑦1 , 3𝑝𝑧1 , 3𝑑1 , 3𝑑1 3𝑑1 as
(3rd excited state) N2 : 𝐾𝐾(𝜎2𝑠)2 ( ∗𝜎 2𝑠)2 (𝜋2𝑝𝑥 )2
Chlorine atom, in its third excited state, reacts 2
= (𝜋2𝑝𝑦 ) (𝜋2𝑝𝑧 )2
with fluorine to form ClF7 . Its shape is pentagonal
N2− ion is formed when N2 accept an electron
bipyramidal.
hence it has15 electrons. The molecular orbital
100 (c)
electronic configuration of the molecule is as
Anion (O− ) repels the test electron because of 2
same charge. N2− : 𝐾𝐾(𝜎2𝑠)2 ( ∗𝜎 2𝑠)2 (𝜋2𝑝𝑥 )2 (𝜋2𝑝𝑦 )
101 (c) (𝜎2𝑝𝑧 )2 ( ∗𝜋 2𝑝𝑥 )1
Cl in ClF3 has 𝑠𝑝3 𝑑-hybridization Hence, this electron goes to antibonding 𝜋
molecular orbital.
108 (b)
The size of isoelectronic decreases with increase
in atomic number.
109 (a)
The bond orders for H2 , H2+ , He2 and He+ 2 are 1.0,
0.5, 0.0 and 0.5 respectively.
and possesses two axial Cl— F bonds and one 110 (b)
equatorial bond. Two lone pairs are at equatorial N atom has smallest radius.
position give rise to bent ‘T’ shape to ClF3 . 111 (d)
103 (c) The order of screening effect for a given shell
−
O2 has one unpaired electron in its antibonding electrons is 𝑠 > 𝑝 > 𝑑 > 𝑓.
112 (a)
The stability of hydrides decreases down the gp,
𝑖. 𝑒., from NH3 to BiH3 which can be observed
from their bond dissociation enthalpy. The correct
order is
NH3 < 𝑃H3 < 𝐴𝑠H3 < 𝑆𝑏H3 < 𝐵𝑖H3
Property NH3 PH3 AsH3 SbH3 BiH3
∆diss 𝐻− (𝐸 − 𝐻)/kJ mol−1 389 322 297 255 −
113 (a)
SF4 has𝑠𝑝3 𝑑2 -hybridization and see-saw
geometry.
114 (a)
Due to presence of intermolecular hydrogen
bonding in H2 O, its molecules are associated with
each other which results unusual high boiling
point of water.
115 (c)
Larger is anion, more is covalent character.
116 (a)
Molecular orbital configuration of,
O2−2
= σ1𝑠 2 , σ∗ 1𝑠 2 , σ2𝑠 2 , σ∗ 2𝑠 2 , σ2𝑝2 , π2𝑝𝑥2 , π2𝑝𝑦2 , π∗ 2𝑝𝑧2 , π∗ 2𝑝𝑦2
117 (a)
Valencies of X, Y and Z is +2, +2 and -2
respectively so, they will form a compound having
of formula 𝑋𝑌𝑍2 .
118 (a)
The molecule in which the bond dipoles of all the
120 (c)
bonds are cancel out by each other, is called non –
Methyl group has +𝐼 effect and−NO2 group
polar e.g., CCl4.
has−𝐼 effect. Therefore, in p-nitro toluene the
InCCl4, there is a large difference between the
dipole moments of – CH3 and−NO2 groups act in
electronegativities of C and Cl but all the four C −
the same direction. So, the resultant dipole
Cl bond dipoles cancel each other , hence it is a
moment is additive.
non-polar molecule.
i.e., 3.93+0.43=4.36 debye
119 (c)
Tetrahedral structure is associated with 𝑠𝑝3 121 (a)
hybridised central atom without any lone pair. The tendency to show lower ionic state increases
The structure of all the compounds given are as down the group due to inert pair effect.
follows : 122 (b)
CH ≡ C − CH2 − CH3
𝑠𝑝 𝑠𝑝 𝑠𝑝3 𝑠𝑝3
In butyne – 1, there is no carbon with 𝑠𝑝2
hybridisation.
123 (b) 132 (d)
2 Paramagnetic species have unpaired electrons
𝜋2𝑝 𝑦
NO+ : σ1𝑠 2 , σ𝑥 1𝑠 2 , σ2𝑠 2 , σ𝑥 2𝑠 2 , σ2𝑝𝑥2 [ ] B. O.
𝜋2𝜋𝑧2 133 (c)
10 − 4 N in it has three σ-bonds and one lone pair of
= =3
2 electron.
134 (a)
CN − : Electron deficient species can accept lone pair of
2
𝜋2𝑝 𝑦 electron and thus, act as Lewis acid.
σ1𝑠 2 , σ𝑥 1𝑠 2 , σ2𝑠 2 , σ𝑥 2𝑠 2 , σ2𝑝x2 [ ] B. O. =
𝜋2𝑝𝑧2 135 (a)
10−4 NH3 has pyramidal shape and thus, possesses
=3
2
three folds axis of symmetry.
124 (c)
136 (d)
Electron affinity order for halogens is Cl > 𝐹 >
ICl− 3
2 has𝑠𝑝 𝑑-hybridization and has two bond
𝐵𝑟 > 𝐼.
pairs and three lone pairs of electrons.
125 (d)
137 (a)
Sulphur trioxide has no S − S linkage. It has
The dipole moment of a polar molecule depends
triangular planar geometry.
upon its geometry. A symmetrical molecule is
non-polar even though it contain polar bonds.
Methane molecule (CH4 ) has zero moment value
of dipole moment due to its symmetrical
structure.
In CHCl3, the resultant of C – H and C – Cl dipole
oppose the resultant of two C – Cl dipoles while in
127 (d)
CH2 Cl2 , the resultant of C – H dipoles adds to
All molecules or ions 𝑖. 𝑒.,
+ resultant of two C – Cl. In case CH3 Cl, the resultant
H2 O, NH4, SO2− −
4 , ClO4 , and NH3 are involved in 𝑠𝑝
3
of two C – H dipole adds to the resultant of two C
hybridisation in their formation.
– Cl. In case CH3 Cl the resultant of two C – H
129 (b)
dipoles add to the resultant of C – H and C – Cl
𝑝-orbitals always show lateral overlapping.
dipoles.
130 (a)
Thus dipole moment of CH3 Cl is highest among
SF6 does not obey octet rule as in it S-atom has 12
the given compounds. The molecule (CCl4) again
electrons in its valence shell.
becomes symmetrical and dipole moment reduces
to zero.
138 (c)
S in SCl4 is 𝑠𝑝3 𝑑-hybridized and possesses see-
saw structure whereas SiCl4 is tetrahedral.
131 (b)
The structure of peroxodisulphuric acid (H2 S2 O8 )
is
139 (c)
Oxygen cannot expand its octet due to absence of
𝑑-orbitals in its valence shell.
142 (a)
Geometry is explained by taking an account of
single bonds only. However, presence of double
Hence, it contains 11σand 4π-bonds. bond may distort bond angles, 𝑒.g., HCHO has 𝑠𝑝2 -
hybridization but angle H—C—H is 116 and covalent bonding.
angle H—C—O is 122 due to double bond. In 159 (b)
BF3 (𝑠𝑝2 -hybridization) each angle is of 120. SF4 has𝑠𝑝3 𝑑-hybridized sulphur atom.
143 (d) 160 (c)
The shape of carbon dioxide is linear because it SbCl2− 3 2
5 has𝑠𝑝 𝑑 –and rest all has 𝑠𝑝 𝑑-
3
204 (c)
Spec Structure 𝑙𝑝 𝑏𝑝 VSE Bond
ies PR angle
Hence, (m-nitroaniline) has the 2 2 𝑙𝑝 90°
H2 S 1 3 − 𝑙𝑝 107°
highest dipole moment among the given.
0 3 𝑙𝑝 120°
196 (a) 0 4 − 𝑏𝑝 109°28′′′′′′′′′′′′′′′′′′
Thus, excitation of 2𝑠-electron in N is not possible. NH3 𝑏𝑝
197 (b) − 𝑏𝑝
PF5 has 𝑠𝑝3 𝑑 hybridization (trigonal bipyramid);
BrF5 has 𝑠𝑝3 𝑑2 hybridization (square pyramidal) BF3 𝑙𝑝
198 (d) − 𝑏𝑝
SiH4 𝑏𝑝
In NH3 𝑠𝑝3 hybridisation is present but its shape
− 𝑏𝑝
becomes pyramidal due to the presence of one
lone pair of electron. 𝑏𝑝
− 𝑏𝑝
𝑏𝑝
199 (d) − 𝑏𝑝
Higher the lattice energy lower the solubility. Out
of the four combinations possible, the lattice Thus, bond angle H2 S < 𝑁H3 < 𝑆𝑖H4 < 𝐵F3 .
energy of MgS (bi-bivalent ionic solid) is higher 205 (d)
than those of Na2 S, MgCl2 (uni-bivalent or biuni- The pyramidal structure of covalent molecule 𝐴𝐵3
valent ionic solids ) and NaCl (uni-univalent ionic is as :
solids) and hence, MgS is the least soluble.
200 (b)
Athree electrons in its outermost orbit, its valency
is 3. B has six electrons in its outermost orbit, its
π2𝑝𝑦1
B2 ∶ σ1𝑠 2 , σ∗ 1𝑠 2 , σ2𝑠 2 , σ∗ 2𝑠 2 [ ]
π2𝑝𝑧1
6−4
B.O. = 2
=1
216 (c)
In the formation of 𝑋𝑒𝐹6 molecule, three 5 p
No. of lone pair = 1 electrons are promoted to 5dorbitals. Now, one
No. of bond pair =3 5s, three 5p and three 5d-orbitals of Xe atom
207 (d) intermix together and form seven 𝑠𝑝3 𝑑3 hybrid
𝑑 2 𝑠𝑝3 -leads to octahedral geometry. orbitals. One 𝑠𝑝3 𝑑3 hybrid orbital contains one
209 (a) lone pair of electrons while other six are half-
A molecule is said to possess a three-fold axis of filled. The expected geometry is pentagonal
symmetry if on rotation around this axis through bipyramidal.
an angle of 360/3, 𝑖𝑒, 120°,gives the same
arrangement of atoms. Since NH3 has a pyramidal
geometry, therefore, it has a three fold axis of
symmetry
210 (a)
Proton number does not change in ion formation,
though number of electrons and size change
during this.
211 (d)
Valence bond theory (Resonance theory) of
metallic bond was given by Pauling (1937).
According to this theory, the metallic bonding is
217 (a)
essentially covalent in origin and metallic
CaC2 ⇌ Ca2+ + C22−
structure exhibits resonance of electro-pair bonds
Carbide ion
between each atom and its nearest neighbours. In
In carbide ion, two carbon atoms are joined by
other words, there is a resonance of a large
triple bond
number of canonical forms.
(If is isoelectronic with N2 )
212 (c)
−C ≡ C −
Notice configuration of N + , C + , O+ and F +.
with two π and one σ-bonds.
213 (b)
218 (b)
ClF3 has𝑠𝑝3 𝑑 hybridisation. Out of five 𝑠𝑝3 𝑑
H2 Ohas𝑠𝑝3 -hybridization.
hybrid orbitals two are completely filled by 𝑙𝑝and
219 (c)
three are half filled which overlap with
𝑒. g. , BF3 , a non-polar molecule having 𝑠𝑝2 -
three2𝑝𝑧 half filled orbitals of three F-atoms. Due
hybridization.
to the presence of two 𝑙𝑝𝑠its geometry is bent 𝑇-
220 (b)
shaped.
When there is less difference in
electronegativities of two atoms (but
electronegativities are not same) and large
difference in their size, polar covalent bond forms.
H and Br : Small difference in electronegativities
and large difference in size. Hence, form polar
214 (d)
covalent bond.
These are characteristics of resonance.
Na and Br : large difference in electronegativities,
215 (c)
2 ∗ 2 hence electrovalent bond is formed.
2 π2𝑝𝑦 π 2𝑝𝑦
O2−
2 ∶ σ1𝑠 2 ∗
, σ 1𝑠 2
, σ2𝑠 2 ∗
σ 2𝑠 2
σ2𝑝 [ ] 221 (b)
π2𝑝𝑧2 π∗ 2𝑝𝑧2
10−8 The bond order for O2− − +
2 , O2 , O2 , O2 are 1.0, 1.5,
B.O. = =1
2 2.0, 2.5 respectively. Higher is bond order, more is
bond energy.
222 (c) Ionic radius : Na+ > 𝑀g 2+ > 𝐴l3+
In XeF4 , the central atom, Xe, has eight electrons 237 (c)
in its outermost shell. Out of these four are used 1, 4-dihydroxy benzene shows the highest boiling
for forming four σ-bonds with F and four remain point among given compounds because it forms
as lone pairs. strong intermolecular hydrogen bonds (It does
∴ XeF4 ⟹ 4 σ bonds + 2 lone pairs not form intermolecular H-bonding.)
3 2
⟹ 6 bybridised orbitals, 𝑖. 𝑒. , 𝑠𝑝 𝑑 hybridisation
Since, two lone pairs of electrons are present, the
geometry of XeF4 becomes square planar from
octahedral.
9. XeF2 , CO2
276 (c)
Species having the same number of electron, have
same bond order.
Species Number of
electrons
CN − 6+7+1=14
O−2 8+8+1=17
∴ Both have different structure. NO+ 7+8-1=14
CN − 6+7-1=12
10. PF5 , IF7
Since, CN − and NO+ have same number of
electrons, they have same bond order, 𝑖. 𝑒., 3.
CN − or NO+ = 14=
𝜎1𝑠 , 𝜎 1𝑠 , 𝜎2𝑠 , 𝜎 2𝑠 2 , 𝜎2𝑝𝑧2 , 𝜋2𝑝𝑥2 ≈ 𝜋2𝑝𝑦,
2 ∗ 2 2 ∗ 2
𝑁𝑏− 𝑁𝑎 (a) CH4 ⟶ CH3 − CH3
Bond order = 2
10 − 4 4 bp + 0 lp 4bp4bp
= = 3. Hybridisation𝑠𝑝 𝑠𝑝 𝑠𝑝3 3 3
2
Structure tetrahedral tetrahedral
277 (c) (b)NH3 ⟶ NH4+
3bp+ 1lp 4bp
3 3
Hybridisation𝑠𝑝 𝑠𝑝
Structure pyramidal tetrahedral
In water molecule the H − O − H bond angle is (c)BF3 ⟶ BF4−
104.5° and dipole moment is 1.84 D. 3bp 4bp
The bond angle of H2 O is lower than 109.28′′ due Hybridisation𝑠𝑝2 𝑠𝑝3
to the presence of two lone pair of electrons on Structure trigonaltetrahedral
the oxygen atom. planar
278 (d) (d)H2 O ⟶ H3 O+
Follow text. 2bp+ 2lp 3bp+ 1lp
3 3
279 (a) Hybridisation𝑠𝑝 𝑠𝑝
𝑅CH2 NHCH3shows the hydrogen bonding, since H Structure angularpyramidal
is attached to N atom. Thus conversion of BF3 into BF4− involves change
280 (c) in both hybridisation and shape.
Clatom has 17 electrons, Cl− ion has 18 electrons. 287 (a)
281 (a) In O2 molecule, the total number of electrons = 16
High boiling point. of water is due to dipole-dipole Electronic distribution in molecular orbital of
interaction. O2
282 (d) = 𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜎2𝑝𝑥2 (𝜋2𝑝𝑦2 , 𝜋2𝑝𝑧2 )
Ionisation enthalpy increases along the period , ( ∗𝜋 2𝑝𝑦1 , ∗𝜋 2𝑝𝑧1 )
and decreases down the group. 1 1
Bond order in O2 = [𝑁𝑏− 𝑁𝑎 ] = [10 − 6] = 2.0
283 (b) +
2 2
In O2 =𝜎1𝑠 , 𝜎 1𝑠 , 𝜎2𝑠 , 𝜎 2𝑠 , 𝜎2𝑝𝑥2
2 ∗ 2 2 ∗ 2
The jump in IP values exist in IP5 and thus,
removal of fifth electron occurs from inner shell. (𝜋2𝑝𝑦2 = 𝜋2𝑝𝑧2 ), ( ∗𝜋 2𝑝𝑦1 )
𝑁𝑏− 𝑁𝑎 10−5
Thus, element contains four electrons in its Bond order in O+ 2 = = = 2.5
2 2
valency shell. 288 (a)
284 (a) Percentage ionic character
Paramagnetic species has unpaired electron. experimental value of DM
B2 = 5 + 5 = × 100
theoretical value of DM
= 10 𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜋2𝑝𝑥1 = 𝜋2𝑝𝑦1 1.03
= × 100 = 17%
C2 = 6 + 6 = 12 6.12
= 𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜋2𝑝𝑥2 = 𝜋2𝑝𝑦2 289 (b)
Electron affinity decreases down the group, but
N2 = 7 + 7 = 14
‘O’ has small atomic size and 2𝑝-orbital becomes
= 𝜎1𝑠 2 , ∗𝜎 1𝑠 2 𝜎2𝑠 2 , ∗𝜎 2𝑠 2, 𝜋2𝑝𝑥2
very compact and already has 6 electrons, hence,
= 𝜋2𝑝𝑦2 , 𝜎2𝑝𝑧2
there is a repulsive force among the already
F2 = 9 + 9 = 18
present and added electrons. Some of the energy
= 𝜎1𝑠 2, ∗𝜎 1𝑠 2 , 𝜎2𝑠 2, ∗𝜎 2𝑠 2 , 𝜎2𝑝𝑧2 , 𝜋2𝑝𝑥2
evolved, due to addition of electron, is used to
= 𝜋2𝑝𝑦2 , ∗𝜋 2𝑝𝑥2 = ∗𝜋 2𝑝𝑦2
reduce the repulsion. Hence, the E.A. of O is less
∴ B2 is paramagnetic because it has unpaired than S, so the order is S > 𝑂 > 𝑆𝑒.
electron. 290 (a)
285 (a) A 𝜋-bond has a nodal plane passing through the
Na ⟶ Na+ +e; 𝐼𝐸 of Na = +ve two bonded nuclei, 𝑖. 𝑒., molecular plane.
Na+ + 𝑒 ⟶ Na; 𝐸𝐴 of Na+ =-ve
Both are equal but opposite in nature.
286 (c)
299 (c)
Stronger is metallic bonding (Fe has 𝑑-subshell),
more is hardness.
300 (d)
291 (c) Compound Bond angle
Electronegativity of elements increases along the NH3 107°
period and decreases down the group. PCl3 93°
292 (b) BCl3 120°
In CO2 , C-atom is 𝑠𝑝-hybridised, thus it has linear 301 (d)
structure. In XeF2 , Xe is 𝑠𝑝3 𝑑 hybridised with In propyne there are 2 π − bonds and six sigma
three lone-pairs of electrons on equatorial bonds.
position. This minimises repulsion, hence it has CH3 C ≡ CH
also linear structure. 302 (a)
293 (b) Like atoms results in covalent bonding leading to
Structure of CO2 is linear due to 𝑠𝑝-hybridisation. the formation of non-polar bond, 𝑒. g. , H—Hor H2 .
(𝑠𝑝) 303 (c)
O=C=O OO
294 (a) ||||
Higher the bond order short the bond length O2+ 2 CH3 − C − OHCH3 − C − NH2
has the shortest the bond length (BO=3) 𝑠𝑝2 𝑠𝑝2
Bond order of remaining species are :
O+ − 2−
2 (2.5), O2 (1.5)andO2 (1) OH
295 (b) |||
11. The first bond between any two atoms is σ CH3 − C − OHCH3 − C − CH2
and rest areπ bonds. |𝑠𝑝2
H
12. πbond is formed by sideways overlapping 𝑠𝑝2
of unhybridised 𝑝-orbital.
304 (d)
428 (b)
It is the order of stability.
429 (b)
420 (b) 𝐸1 forHe+ = 𝐸1 for 𝐻 × Z2 (where Z=at.no. of He).
Lower potential energy level imparts stability. 430 (c)
421 (d) H—bonding order:
1 ⋯H − F > ⋯H − O > ⋯H − N
Covalent character ∝
size of cation 431 (d)
∝ size of anion The charge-size ratio increases and thus
(according to Fajan’s rule) polarizing power increases.
Lower the covalent character, higher will be ionic 434 (c)
character. O2 has two unpaired electrons.
Cl2 O, contains O2− , NCl3 contains N 3− 435 (d)
, PbCl2 contains Pb2+ and BaCl2 contains Ba2+ . These are the factors on which IP depends.
Hence, the order of covalent character is 436 (b)
NCl3 > 𝐶l2 O > 𝑃𝑏𝐶l2 > 𝐵𝑎𝐶l2 The hybridised states of N in NO+ − +
2 , NO3 and NH4
∴ BaCl2 has the greatest ionic character. 2 3
are 𝑠𝑝, 𝑠𝑝 and 𝑠𝑝 respectively.
422 (c)
437 (b)
Carbon (1) has 2σ − and 2μ − bonds. Carbon (2)
has 3σ and 1 π-bond.
438 (c)
According to Fajan’s rule, as the size of cation ∴ In benzene, the carbon – carbon bond is
decreases, its polarising power increases. Hence, between the double and single bond due to the
Cu2+ polarise Cl− ions more than Cu+ . Therefore, resonance, so its bond order is 1.5.
CuCl2 has more covalent character and hence, its 448 (a)
boiling point is less. If difference in electronegativity in between two
439 (b) atoms is 1.7, the molecule possesses 50%
Metals are more electropositive and lose covalent +50% ionic nature.
electrons, while non – metals have tendency to 449 (b)
gain electron. IP1 ofPb > 𝐼P1 of Sn (an exception).
440 (b) 450 (c)
Behas smallest size and thus, Be cation possesses Only then it can accept lone pair in that shell.
more polarizing power. 451 (a)
441 (b) Count σ-and π-bonds.
Due to intermolecular hydrogen bonding in 452 (b)
𝑜𝑟𝑡ℎ𝑜-isomer, it has least melting point. Due to The molecular electronic configuration of O2 is
2
effective intermolecular hydrogen bonding in O2 = [𝐾𝐾, (𝜎2𝑠)2 , ( ∗ 2 2
𝜎 2𝑠) , (𝜎2𝑝𝑥 ) , (𝜋2𝑝𝑦 )
1
𝑝𝑎𝑟𝑎 isomer, it has highest melting point among = (𝜋2𝑝𝑧 )2 , ( ∗
𝜋 2𝑝𝑦 ) = (𝜋2𝑝𝑧 ) ]
1
the isomers. So, the order is 453 (d)
𝑃𝑎𝑟𝑎 isomer >𝑚𝑒𝑡𝑎>𝑜𝑟𝑡ℎ𝑜 Csis more electropositive.
(114℃)(97℃) (54 ℃ ) 454 (a)
443 (a) In MnO− 4 , the oxidation no. of Mn is +7, 𝑖. 𝑒., all the
Based on geometry of molecule. 4𝑠 and 3𝑑 electrons are lost.
444 (b) 455 (d)
The structure of these molecules/species are as Stability ∝ bond order
follows : 456 (b)
Charge of 𝑒 − = 1.6 × 10−19 C
Dipole moment of HBr = 1.6 × 10−30 C-m
Interionic spacing = 1 Å = 1 × 10−10 m
% of ionic character in
Dipole moment of HBr × 100
HBr =
Interspacing distance × 𝑞
1.6 × 10−30 × 100
=
1.6 × 10−19 × 10−10
= 10−30 × 1029 × 100 = 0.1 × 100 = 10%
457 (c)
Due to shielding effect of (𝑛−1)𝑑-subshell.
PCl3 has𝑠𝑝3 -hybridisation but due to presence of a 459 (d)
lone-pair, its shape is pyramidal instead of P in PO3− 3 2−
4 has 𝑠𝑝 -hybridization like S in SO4 .
tetrahedral. 460 (d)
446 (c) The lattice becomes stronger (i.e., the lattice
[C]forms anion readily by gaining one electron energy Ubecomes more negative). As r the
only. interionic distance decreases. U is proportional to
447 (c) 1
Number of bonds between two atoms is called 𝑟
1
bond order. or 𝑈 ∝ (𝑟 +𝑟
𝑐 𝑎)
Resonating structures of benzene are 462 (a)
Covalent radius are always smaller than crystal
radius as the former involves overlapping region.
463 (c)
CO2−
3 has the following structure
487 (b)
18. CH4 π2𝑝𝑥 andπ2𝑝𝑦 or ∗π 2𝑝𝑥 and ∗π 2𝑝𝑦 orbitals have
1
𝐻=2 (4+4+0-0) nearly equal energy and thus, are called
degenerate orbitals.
8 488 (a)
=2=4
The most electronegative element is F and next to
∴ 𝑠𝑝3 hybridisation F is O.
489 (c)
19. BCl3 Ions are held in NaCl by coulombic forces and
thus, possess no velocity.
1
𝐻=2 (3+3+0-0) 490 (b)
Both have one lone pair of electron.
6
=2=3 491 (d)
𝑞 𝑞
Lattice energy,𝑈 = 𝑟1 2 2
∴ 𝑠𝑝3 hybridisation
Since, interionic distances in CaO and NaCl are
20. NH3 similar, (larger cation has smaller anion and vice
versa) 𝑟 is almost the same. Therefore, lattice
1
𝐻= (5+3+0-0) energy depends only on charge. Since, the
2
magnitude of charge on Na+ and Cl− ions is same
8
= =4 𝑖𝑒, unity and that on Ca2+ and O2− ions is 2 each,
2
therefore, the lattice energy of CaO is four times
∴ 𝑠𝑝3 hybridisation the lattice energy ofNaCl,𝑖𝑒,4U
492 (a)
∴ (c) is correct answer.
528 (a)
21. 𝑑𝑠𝑝3 or 𝑠𝑝3 𝑑hybridisation results in
trigonal bipyramidal geometry according
to VSEPR theory.
582 (d)
All carbon to hydrogen bonds are σ-bonds 591 (b)
583 (b) 𝐼𝐸1 of N > 𝐼𝐸1 of O due to half filled nature in N.
In C2 H6 , Cis 𝑠𝑝3 hybridised. 592 (b)
In C2 H4 , Cis 𝑠𝑝2 hybridised. Larger anion is easily deformed (Follow Fajans’
In BeCl2 , Beis 𝑠𝑝 hybridised. rule).
In C2 H2 , Cis 𝑠𝑝 hybridised 593 (c)
584 (b) Due to resonance structure of C6 H6.
Energy bonds in solids are formed in accordance 594 (d)
with Bohr’s theory. Draw bond structure and then count bonds.
585 (c)
The jump in ionisation energy occurs when
valence shell changes during removal of electron.
586 (c)
H atom attached on F is responsible for H-
bonding..
⟹ 12σ, 2dπ − pπbonds.
587 (a)
595 (a)
In methane, ethene and ethyne, the hybridisations
are respectively 𝑠𝑝3 , 𝑠𝑝2 and 𝑠𝑝. Hence, % 𝑠-
character will be
1
𝑠𝑝3 = × 100 = 25%
4
Bond length increases when bond order decrease, 1
2
hence the correct order of bond length is 𝑠𝑝 = × 100 = 33%
3
CO2−
3 > 𝐶O2 > 𝐶𝑂 1
𝑠𝑝 = × 100 = 50%
588 (a) 2
3
In PCl3 molecule, phosphorus is 𝑠𝑝 -hybridised 597 (c)
but due to presence of lone-pair of electron. It has Both SO2− − 3
4 and BF4 have 𝑠𝑝 -hybridization and
pyramidal structure. are tetrahedral.
598 (c)
If there is four σ − bonds, hybridisation is 𝑠𝑝3 , if
three σ − bonds, hybridisation is 𝑠𝑝2 and if two
σ − bonds, hybridisation is sp. It is the definition of valency.
(a) CH2 = C = CH2 607 (a)
𝑠𝑝2 sp𝑠𝑝2 Only Na shows +1 oxidation state. Rest all have
(b)CH3 − CH = CH − CH2+ +1, +2(Hg), +1, +2 (Cu) and +2, +3 (Fe)
𝑠𝑝3 𝑠𝑝2 𝑠𝑝2 𝑠𝑝2 oxidation states.
(c)CH3 − C ≡ C − CH2+ 608 (a)
𝑠𝑝3 𝑠𝑝 𝑠𝑝 𝑠𝑝2 The ionisation energy of elements decreases
(d)CH3 − CH = CH − CH2− down the group.
𝑠𝑝3 𝑠𝑝2 𝑠𝑝2 𝑠𝑝3 609 (d)
(e)CH2 = CH − CH = CH2 O is more electronegative than C.
𝑠𝑝2 𝑠𝑝2 𝑠𝑝2 𝑠𝑝2 610 (c)
Hence, in CH3 − C ≡ C − CH2+ , all the three types Bond energy increases with multiplicity of bonds.
of hybrid carbons are present. 611 (c)
599 (b) Br2 is a non-polar molecule and hence, its melting
Sigma bond formation involves more overlapping point and boiling point depend only upon van der
and thus stronger. Waals’ forces of attraction while all the remaining
600 (b) molecules have dipole moments and hence, their
Both have 𝑠𝑝2 -hybridization geometry. melting points and boiling points depend upon
601 (b) dipole-dipole interactions
Anions are always larger than their parent atom. 612 (c)
Also atomic radius increases down the group, H-bonding in H2 O increases forces of attracting
decreases along the period. among molecules and develops abnormal
602 (c) properties.
AsF5 has sp3 𝑑 hybridization. In 𝑠𝑝3 𝑑 614 (b)
hybridization, it is 𝑑𝓏 2 orbitals which takes part In a double bond ( = )oneσandon𝑒 π-bond is
603 (a) present while in a single bond ( − ) only σ-bond is
present.
The structure of the naphthalene is as
CCl4and compounds has
zero dipole moment due to their symmetrical
structure.
604 (b)
Ionisation energy increases along the period.
605 (a)
In octahedral structure 𝑀𝑋6 , the six hybrid In naphthalene five double bonds are present,
orbitals (𝑠𝑝3 𝑑2 ) are directed towards the corners hence 5π bonds are present in naphthalene.
of a regular octahedral with an angle of 90°. 616 (d)
According to following structure of 𝑀𝑋6 the ICl− − −
2 , I3 , N3 are linear
number of 𝑋 − 𝑀 − 𝑋 bonds at 180° must be but
three. ClO− 3
2 is angular due to 𝑠𝑝 hybridisation of Cl atom.
So, ClO−
2 is non-linear.
617 (c)
1
Bond order = [bonding electrons – antibonding
2
electrons]
618 (c)
The difference of electronegativity is more.
606 (a) 619 (c)
𝑂𝑟𝑡ℎ𝑜hydroxyl benzaldehyde has maximum expected to be covalent
volatility due to intra molecular H-bonding. 634 (a)
620 (b) SiF4 and SF4 are not isostructural because SiF4 is
Formal charge = Number of electrons in valence tetrahedral due to 𝑠𝑝3 hybridisation of Si while
shell – SF4 is not tetrahedral but it is distorted
1
(2 ×numbers of electrons as bond pair+numbers tetrahedral because in it S is 𝑠𝑝3 𝑑 hybridised and
of electrons as lone pair) has a lone pair of electron.
635 (c)
SiF4 has regular tetrahedral geometry.
636 (d)
For N1 and N3
4 Clpossesses 10 electrons in ClF3 .
Formal charge = 5 − (2 + 4) = 5 − (6) = −1
637 (a)
1
For N2 = 5 − × 8 − 0 = 5 − 4 = +1 Molec 𝑏𝑝 Hybridisa Shape
2
621 (d) ule + 𝑙𝑝 tion
H2 O 2 +2 𝑠𝑝3 Angular
In phenol each C atom is 𝑠𝑝2 hybridised andO
Trigonal
atom is 𝑠𝑝3 hybridised. BCl3 3 + 0 𝑠𝑝2 Planar
622 (a) NH4 +
4 + 0 𝑠𝑝3 Tetrahedral
Due to 𝑠𝑝3 -hybridization on carbon atoms. CH4 4 + 0 𝑠𝑝3 Tetrahedral
623 (b) 638 (c)
Bond angles of ClF3 , PF3 , NF3 and BF3 are (180, Electronegativity and ionisation energy decreases
90), (101), (106) and (120) respectively. from F to I.
624 (c) 639 (d)
Operates in each gaseous molecule. CH ≡ CH; 3for triple bonds and two for C—H
625 (d) bond.
Resultant of two opposite vectors produces zero 640 (b)
dipole moment. The electronic configuration of O2− 2 ion is
2−
626 (d) O2
Because of its regular tetrahedral geometry, CCl4 − 𝜎1𝑠 2 , ∗𝜎 1𝑠 2 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜎2𝑝𝑧2 , 𝜋2𝑝𝑥2 , 𝜋2𝑝𝑦2 , ∗𝜋 2𝑝𝑥2 ,
has least dipole moment Hence, number of antibonding electron pair in
627 (b) O2−
2 molecular ion are four.
Coulombic forces are strongest among all. 641 (c)
628 (a) Due to the presence of d-subshell electrons.
CO2 has linear structure. It has 𝑠𝑝-hybridisation 642 (b)
O=C=O Due to 𝑠𝑝2 -hybridization.
629 (a) 643 (a)
In (𝐴) 𝑝𝑎𝑟𝑎-nitro phenol intermolecular M.O. configuration of O2 :
(between two molecules) H-bonding exists while 2 ∗ 2
2 ∗ 2 2 2 2 π2𝑝𝑦 π 2𝑝𝑦
in (𝐵) 𝑜𝑟𝑡ℎ𝑜 –nitrophenol, intramolecular H- σ1𝑠 , σ 1𝑠 , σ2𝑠 , σ ∗ 2𝑠 , σ2px [ ] [ ]
π2𝑝𝑧2 π∗ 2𝑝𝑧1
bonding exists. Molecular orbitals π∗ 2𝑝𝑧 gains electron when O− 2
Because of the presence of intramolecular H- is formed from O2
bonding, the boiling point of (𝐵) is lower as 644 (a)
compare to (𝐴) and thus, (𝐵) is more volatile 𝑖. 𝑒., H-bonding is weakest bonding.
has higher vapour pressure as compare to (𝐴). 646 (b)
630 (b) Out of 𝑠𝑝3 , 𝑠𝑝, 𝑠𝑝2 hybridised carbon, 𝑠𝑝
Small cation has more polarizing power. hybridised carbon is more electronegative.
632 (c) 647 (c)
Polar solute are more soluble in polar solvents. Both NH3 and H2 O have 𝑠𝑝3 -hybridization.
633 (b) CO2 andBeCl2 are linear (𝑠𝑝-hybridization).
Since, the electronegativity (EN) different is 3.0 − 648 (d)
1.2 = 1.8, which is less than 1.9, therefore, bond is Unpaired electrons give rise to paramagnetism.
649 (a) Molecules Interaction
HF has largest dipole moment because Benzene and Dispersion force
electronegativity difference of both is high so, it is ethanol Dipole-dipole
highly polar Acetonitrile and Ion-dipole
acetone Dispersion
650 (b)
KCl and water (London) force
Due to H-bonding which is more in water than Benzene and
alcohol and not in ether. carbon
652 (c) tetrachloride
1𝑠 2 , 2𝑠 2 2𝑝4 leads a sharing of two electron pairs 667 (b)
to form molecule, 𝑒. g., O2 . Dry ice is CO2 having C—O covalent bonds.
654 (b) 668 (d)
Count σ and π bonds.
655 (c)
Bond orderC2− > 𝑁𝑂 > O− 2 > 𝐻e2
+
690 (c)
∴ Total electrons in NH3 =5+1+1+1=8
683 (d)
The electronic configuration of carbon is
1𝑠 2 , 2𝑠 2 2𝑝2 .
684 (c)
Number of hybrid orbitals= no. of bp + no. of 𝑙𝑝
=5+1=6
Peroxide ion in O2− 2
O2−
2 (18) = σ1𝑠 2
, ∗ 2
σ 1𝑠 ,
2
σ 2𝑠 ,
∗ 2 2
σ 2𝑠 , σ2𝑝𝑧
π2𝑝𝑥2 = π2𝑝𝑦2 , ∗π 2𝑝𝑥2 = ∗
π 2𝑝𝑦
2
𝑁𝑏 −𝑁𝑎 10−8
Bond order = 2
= 2
=1
It contains four completely filled antibonding
molecular orbitals. Since, all the electrons are
paired, O2−
2 is diamagnetic.
Peroxide ion is isoelectronic with argon, not with
Acetonitrile does not contain 𝑠𝑝2 hybridised
neon.
carbon.
701 (b)
691 (b)
BF3 : 𝑠𝑝2 NO− 2 3 − 3
2 ∶ 𝑠𝑝 NH3 ∶ 𝑠𝑝 NH2 : 𝑠𝑝 H2 O ∶ 𝑠𝑝
3
The atomic radii decreases along the period and
702 (b)
increases down the gp.
Multiplicity in bonds decreases bond length.
692 (b)
703 (a)
SiO2possesses giant molecular structure due to
O2−
2 (Total number of electrons =18)
tetra valence and catenation nature of Si.
𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜎2𝑝𝑧2 , 𝜋2𝑝𝑥2
693 (d)
= 𝜋2𝑝𝑦2 ∗𝜋 2𝑝𝑥2 = ∗𝜋 2𝑝𝑦2
According to VSEPR theory the bond angle
decreases with increase in the size of the valence 704 (d)
shell of the central atom because electronegativity IF7
decreases. 𝑖. 𝑒., decreasing order of bond angles is
NH3 > 𝑃H3 > 𝐴𝑠H3 > 𝑆𝑏H3
694 (b)
Half-filled orbitals are more stable.
695 (a)
In BrF5 number of electrons = 6
(1 lp+5 bp)
742 (a)
Electronegativity difference in two atoms
involved in bonding is a measure of polarity in
molecule.
743 (c)
≡ C—has2σ-and 2π- (thus, 𝑠𝑝-hybridization);
−CH= has 3σ- and 1π- (thus, 𝑠𝑝2 -hybridization).
Remember hybridized orbitals do not form π-
bonds.
744 (b)
Fhas 7 electrons in its valence shell. Thus, to
attain stability, it should have lost one electron.
738 (c)
745 (a)
BCl3 has six electrons in outer shell of boron atom.
In O2−
2 , 8 electrons are present in antibonding
739 (b)
orbitals
H2 Scontain only covalent bonds, as the π2p2 π∗ p2
electronegativity difference between H and S is σ1s 2 , σ*1s 2 , σ2s 2 , σ*2s 2 , σ2p2x [ y2 ] , [ ∗ y2 ]
π2pz π 2pz
only (2.6 – 2.1 = 0.5). 746 (a)
CH3+ possesses𝑠𝑝2 -hybridization.
747 (a)
No doubt NH3 and BF3 have 𝑠𝑝3 (pyramidal) and
740 (c) 𝑠𝑝2 (coplanar) hybridization respectively having
3
CCl4has𝑠𝑝 -hybridization giving regular one lone pair of electron on N atom which is
tetrahedron geometry. In others the geometry is responsible for pyramidal shape of NH3 inspite of
little distorted inspite of 𝑠𝑝3 -hybridization due to 𝑠𝑝3 hybridization. However, as soon as it is
different atoms on the vertices of tetrahedron. coordinated to BF3 , both attain tetrahedral
741 (b) geometry and acquire 𝑠𝑝3 -hybridization.
P undergoes 𝑠𝑝3 𝑑 hybridisation in PCl5 and it has 748 (b)
trigonal bipyramidal structure Nitrogen molecule has highest bond energy due to
presence of triple bond
749 (b)
P4 O6has following structure.
Thus, every P-atom is linked to 3 oxygen atoms.
O
O
Cl
2
752 (a)
1
CN − and NO+both have same number of electrons Cl P
753 (b)
1 4
Bond length ∝ Cl
bond order
754 (c) Cl
764 (a)
Each possesses 18 electrons.
Total number = 4⟶ 𝑠𝑝3 hybridisation
766 (d)
He+ −
2 (B. O. = 0.5) < O2 (B. O. = 1.5)
< 𝑁𝑂(B. O. = 2.5) < C22− (B. O.
= 3.0)
Total number = 5⟶ 𝑠𝑝3 𝑑hybridisation 768 (d)
In SO3 molecules, S-atom remains 𝑠𝑝2 hybrid,
hence, it has trigonal planar structure
𝑠𝑝3 hybridisation
769 (d)
BCl3 = 3σ bonds+0𝑙𝑝 of𝑒 − = 3 ⟹
𝑠𝑝2 hybridisation
NCl3 = 3σ bonds+1𝑙𝑝 of𝑒 − = 4 ⟹
771 (b)
N is 𝑠𝑝2 -hybridized in NO−
3.
772 (d)
The ionic radius increases down the group.
773 (b)
The formula of 𝑀𝑋3 shows the presence of
3σbonds. Since, it has T-shape geometry, it must
contain 2 lone pairs as
783 (a)
P4 O10 is
774 (a)
Except NO− (16 electrons), rest all have 14
electrons.
776 (c)
Ethyl alcohol forms stronger H-bonds than
ethylamine or ammonia due to greater 784 (b)
electronegativity of oxygen than nitrogen atom. The Born-Haber cycle takes place as follows
Diethyl ether, however, does not form H-bonds
since , it does not have a H-atom attached to O-
atom.
778 (c)
Carbon in CO2 has 𝑠𝑝-hybridization.
779 (c)
In both CH4 and CCl4, 𝑠𝑝3 hybridisation is present
and both have tetrahedral geometry.
781 (a)
As the 𝑠-character increases in hybrid orbitals,
bond energy increases, size of the hybridized Hence, 𝑍 is𝑀+ 𝑋 − (𝑠)
orbital decreases. 𝑠-characters in 𝑠𝑝, 𝑠𝑝2 and 𝑠𝑝3 785 (a)
are 1/2, 1/3, 1/4 respectively. S atom is larger in size than O and F.
782 (b) 786 (d)
NH4 Clcontains ionic, covalent and coordinate N2 (7 + 7 = 14) = 𝜎1𝑠 2 , 𝜎 ∗ 1𝑠 2 , 𝜎2𝑠 2 , 𝜎 ∗ 2𝑠 2 , 𝜋2𝑝𝑥2
linkage. ≈ 𝜋2𝑝𝑦2 , 𝜎2𝑝𝓏2
10−4
Bond order = 2 = 3
N2+ (7 + 7 − 1 = 13)
= 𝜎1𝑠 2 , 𝜎 ∗ 1𝑠 2 , 𝜎2𝑠 2 , 𝜎 ∗ 2𝑠 2 , 𝜋2𝑝𝑥2
= 𝜋2𝑝𝑦2 , 𝜎2𝑝𝜋1 (paramagnetic)
Bond order =
9−4
= 2.5 Both NH4+ and BF4− have 𝑠𝑝3 -hybridization.
2
Since, 𝑁2+ has less bond, then N − Nbond gets 793 (a)
NH3 molecule has three fold axis of symmetry
weak
O2 (8 + 8 = 16) because it has 𝑠𝑝3 hybridisation but due to
= 𝜎1𝑠 2 , 𝜎 ∗ 1𝑠 2 , 𝜎2𝑠 2 , 𝜎 ∗ 2𝑠 2 , 𝜎2𝑝𝓏2 , 𝜋2𝑝𝑥2 presence of one lone pair of electron it has
pyramidal structure.
≈ 𝜋2𝑝𝑦2 , 𝜋 ∗ 2𝑝𝑥1 ≈ 𝜋 ∗ 2𝑝𝑦1
10−6 794 (b)
Bond order = 2
=2 Basic character of hydrides decreases down the
O+
2 (8 + 8 − 1 = 15) gp.
= 𝜎1𝑠 2 , 𝜎 ∗ 1𝑠 2 , 𝜎2𝑠 2 , 𝜎 ∗ 2𝑠 2 , 𝜎2𝑝𝓏2 , 𝜋2𝑝𝑥2 795 (b)
≈ 𝜋2𝑝𝑦2 , 𝜋 ∗ 2𝑝𝑥1 NO is paramagnetic in nature
Bond order =
10−5
= 2.5 796 (d)
2
Cation radius increases down the group.
Thus, in the formation of O+
2 from
797 (a)
O2 , paramagnetism decreases but the bond order
According to Born-lande equation
increases
𝑍 + 𝑍 − 𝑒 2 An 1
787 (a) 𝑈= ( − 1)
𝑟node 𝑛
In an antibonding molecular orbital, most of the
Where , U is lattice energy
electron density is located away from the space
𝑟node is interionic distance
between the nuclei, as a result of which there is a
1
nodal plane (𝑖. 𝑒., a plane at which the electron ∵𝑈∝
interionic disance
density is zero) between the nuclei.
∴ Ions should be of small size to have high lattice
energy.
798 (d)
Dipole moment of CH3 OH is maximum in these.
799 (b)
788 (d) Intermolecular H-bonding gives rise to an
Speci Hybridisa Lone Bondin increase in b.p.
es tion of Xe pair on g pairs 800 (b)
Xe H3 BO3 has structure
(a) XeO3 𝑠𝑝3 1 3
(b) XeF4 𝑠𝑝3 𝑑2 2 4
(c) XeF6 𝑠𝑝3 𝑑3 1 6
(d) XeF2 𝑠𝑝3 𝑑 3 2
(Max.)
789 (b)
Boiling point of HF is highest due to H-bonding.
For other halogen acids boiling point increase in
Boron has three bonds thus
the order HCl < 𝐻𝐵𝑅 < 𝐻𝐼. Therefore, most 2
𝑠𝑝 hybrdised. Each oxygen has two bonds and two lone pa
volatile (with Lower b.pt.) is HCl.
801 (d)
790 (b)
Species having same hybridisation show similar
The MO electronic configuration of
geometry.
O−2 (8 + 8 + 1 = 17)
SO2−
4 :Hybridisation of S ⟶ 𝑠𝑝
3
= 𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜎2𝑝𝑧2 , 𝜋2𝑝𝑥2
2 ∗ 2 ∗ 1 ClO− 4 :Hybridisation of Cl ⟶ 𝑠𝑝
3
≈ 𝜋2𝑝𝑦, 𝜋 2𝑝𝑥, ≈ 𝜋 2𝑝𝑦
𝑁 802 (c)
Bond order = 𝑏−𝑁 2
𝑎
Anions are larger in size than their parent atom.
10 − 7 803 (c)
= = 1.5
2 Na+andCl− are formed.
791 (d) 804 (b)
Multiplicity in bonds decreases bond lengths. : −CH3 has 𝑠𝑝3 hybridisation.
792 (a)
electrons, which are filled in such a way that all
molecular orbitals are fully filled, so diamagnetic.
𝜎1𝑠 2 ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 ∗𝜎 2𝑠 2 𝜎2𝑝𝑧2 , 𝜋2𝑝𝑥2
= 𝜋2𝑝𝑦2 , ∗𝜋 2𝑝𝑥2 = ∗𝜋 2𝑝𝑦2
815 (a)
805 (c) Water is an universal solvent.
Glycerol and ethanol both have intermolecular 816 (a)
hydrogen bonding but in glycerol According to Fajan’s rule, as the charge on cation
(CH2 OH. CHOH. CH2 OH) hydrogen bonds per increase its size decreases. As a result its
molecule is more than ethanol (C2 H5 OH). It tendency to polarise anion increases. This brings
increases attraction between the molecules and more and more covalent character to
hence, glycerol is more viscous than ethanol. electrovalent compounds.
806 (a) ∵ AmongAlCl3 , LaCl3 , MgCl2 andCsClsize ofAl3+ is
Larger anion is more polarised. smallest.
807 (a) ∴ Al3+ polarises anion to highest extent.
In ∗𝜋2𝑃𝑥 orbital, two nodal planes are present. ∴ AlCl3 has maximum covalent character.
808 (d) 817 (a)
Hydrogen bond is formed between molecules of C6 H6has regular hexagonal geometry.
compounds having O, F and N with H. 818 (c)
SF6 has six S−F bonds.
819 (a)
Resonating structure can be written only for such
molecules in which multiple bonds are presents,
𝑒g, O3
820 (d)
According to Born-Haber cycle the enthalpy of
formation (∆𝐻𝑓 ) of an ionic compound may be
∵ H2 Sdoes not have O, F or N. given as
∴ It does not form hydrogen bond. 1
∆𝐻𝑓 = 𝑆 + 𝐷 + 𝐼 + 𝐸 + 𝑈
810 (a) 2
Where, I = ionisation energy
NaF has maximum melting point, melting point
S = sublimation energy
decreases with increases in size of halide ion and
E = electron affinity
their bond energy get lower
D = dissociation energy
811 (a)
U = lattice energy of compound
𝑠-orbitals never go for lateral overlapping
Born-Haber cycle is used to determine the lattice
because of non-directional nature.
energy of the compound. It also may be used to
812 (d)
calculate electron affinity of an element.
The metallic character is found in iodine as well as
821 (c)
in astatine (At). Note that metallic character
Element 𝐶 has electronic structure 1𝑠 2 , 2𝑠 2 , 2𝑝5 ,it
increases down the group.
requires only one electron to complete its octet
813 (b)
and it will form anion so it will form electrovalent
Ionization energy increases along the period and
bond
decreases down the group. Also (b) has
822 (a)
[Ne]3𝑠 2 , 3𝑝3 , 𝑖. 𝑒., half filled configuration, being
Hatom has 1𝑠1 configuration. Shielding effect is
more stable and thus, have high ionization energy.
property of penultimate shell electrons.
814 (a)
823 (b)
The correct option is O2− 2 . This species has 18
NO+
2 : The species is linear with 𝑠𝑝-hybridisation. between lone pair and bond pair of electrons).
NO− 2
3 : The species is trigonal planar with 𝑠𝑝 -
hybridisation.
838 (b)
Cl2 involves3𝑝 − 3𝑝 overlapping.
839 (b)
NH4+ : The species is tetrahedral with 𝑠𝑝3 -
Only Sulphur has 𝑑-orbitals.
hybridisation.
840 (c)
ClO− 3
4 has𝑠𝑝 -hybridization on Cl atom.
841 (d)
Due to dipole moment intermolecular forces of
attraction becomes stronger and thus,
liquefaction becomes easier.
824 (d) 842 (d)
+
Both C and N have six electrons. sp3 𝑑-hybridisation leads to trigonal bipyramidal
825 (a) geometry if no lone pair is present, 𝑒.g. , PCl5 ; in
According to Fajans’ rule, polarization of anion is ClF3 geometry is T-shaped due to the presence of
influenced by charge of cation, size of cation. More two lone pair of electron. In XeF2 , geometry is
is the charge on cation, more is polarization of linear due to the presence of three lone pair of
anion. electrons.
826 (b) 843 (a)
Smaller cation causes more polarization of anion. Due to the presence of lone pair on N atom.
827 (a) 844 (a)
1 B2 : Total electrons = 10
Bond order = [no. of bonding electrons-no. of
2
Configuration : σ1𝑠 2 ∗σ 1𝑠 2 σ2𝑠 2 ∗σ 2𝑠 2 π2𝑝𝑥1 =
antibonding electron]
π2𝑝𝑦1
828 (c)
Pauling work on chemical bonding. If Hund’s rule is violated, then
829 (a) σ1𝑠 2 ∗σ 1𝑠 2 σ2𝑠 2 ∗σ 2𝑠 2 π2𝑝𝑥2 = π2𝑝𝑦0
All have linear structure So, diamagnetic
6−4
O = C = O, Cl − Hg − Cl, H − C ≡ C − H Bond order = 2 = 1
830 (d) 845 (a)
A characteristic of metallic bonding. Bonding molecular orbitals possess lower energy
831 (a) levels than antibonding orbitals.
Due to larger differences in electronegativity. 846 (a)
833 (b) Be2+ is smallest and Na+ has largest radius.
3 3
SF4 has𝑠𝑝 𝑑 –hybridization. Rest all have 𝑠𝑝 - 847 (b)
hybridization. Hydrogen bond is strongest in HF due to higher
834 (a) electronegativity of F.
NO has 15 electrons. 848 (d)
835 (d) The structure of H2 O is angular V-shape and has
Ti+has 21 electrons in it. Rest all have 10 𝑠𝑝3 - hybridisation and bond angle is 105°. Its
electrons. dipole moment value is positive or more than
836 (a) zero.
O−2 has one unpaired electron.
837 (a)
Structure of ammonia is pyramidal (Distorted
from tetrahedral to pyramidal due to repulsion But in BeF2 , structure is linear due to 𝑠𝑝-
hybridisation (μ = 0). Thus, due to μ > 0, H2 O is
dipolar and due to μ = 0, BeF2 is non-polar.
849 (d)
These are factors on which effective nuclear
charge depends.
850 (a)
5(on P) + 4(on H)−1=8.
851 (b) 859 (c)
Phosphoric acid has 3 – OH groups, which are N atom in NH3 provides electron pair to H + to
involved in hydrogen bonding . form coordinate or dative bond (H3 N → H).
The type of hydrogen bonding, found , is 861 (d)
intermolecular. Due to this, it is syrupy. Due to H-bonding, 𝑉ice > 𝑉water.
852 (c) 862 (b)
The bond angles areH2 SNH3 SiH4 BF3 The covalent compounds have low melting point
92.6 ͦ 107 ͦ 109 ͦ28′ 120 ͦ due to weaker forces of attraction among them as
853 (b) compared to strong forces of attraction in ionic
The metals have low ionization energy. In a piece compounds.
of metal many free electrons are found which ∵ HCl is covalent compound among CsF, HCl HF
move form one atom to other. The presence of and Li
mobile electrons or oscillation of loose electrons (CsF, HF and LiF are ionic compounds)
are responsible for metallic lusture. ∴ HCl has minimum boiling point.
854 (c) 863 (b)
1
Same spin electrons in two atoms do not take part (i) Hybridisation =2 (no. of 𝑒 − in valence shell of
in bonding. central atom + no. of monovalent atoms + charge
855 (b) on anion – charge on cation)
Molecule Hybridisation
SO3 𝑠𝑝2 (ii) Shape or geometry of molecule depends on
C2 H2 𝑠𝑝 lone pair and bond pair of electrons present in it.
C2 H4 𝑠𝑝2
CH4 𝑠𝑝3 Hybridisation of
CO2 𝑠𝑝
1
Hence, the hybrid state of S in SO3 is similar to N in NH3 = 2 (5 + 3 + 0 − 0) = 4
that of C in C2 H4 .
856 (d) ∴ 𝑠𝑝3 hybridisation.
IO− 3
3 , XeO3 , (𝑠𝑝 hybridisation)pyramidal
PF6− , SF6 (𝑠𝑝3 𝑑2 ) octahedral ∵ It has 3 bond pair and 1 lone pair of electrons,
so it has distorted tetrahedron shape.
BH4− ,NH4+ , SiF4 (𝑠𝑝3 )tetrahedral
CO2− 2
3 (𝑠𝑝 ) trigonal planar 864 (d)
− 2
NO3 (𝑠𝑝 ) trigonal planar 24. The bond angle decreases with decrease
SF4 (𝑠𝑝3 𝑑)𝑠𝑒𝑒 − 𝑠𝑎𝑤 in electronegativity. It results in decrease
Hence, SiF4 and SF4 are not isostructural (same in repulsion between bond pair-bond pair
structure). electrons and bond angle becomes
857 (b) smaller.
PCl3 has 𝑠𝑝3 -hybridisation and possesses one
lone pair on P-atom and three bond pair of 25. Between NH 3 andH2 O, H2 O has smaller
electron bond angle due to presence of two lone
pair of electrons causing more repulsion
among electrons as compared of NH 3
which has only one lone pair of electron.
Hydrides
NH 3 H2 O H2 S H2 Se H2 Te Percentage ionic character
observed dipole moment
Bond angles = × 100
theoretical value of dipole moment
107° 105° 92° 91° 90° 1.03
= × 100 = 16.83%
6.12
H2 Tehas smallest bond angle.
874 (b)
865 (a) Double bond involves the sharing of two electron
In ionic solids, ions exist at lattice points. In pairs or four electrons.
covalent solids atoms lie at lattice points. 875 (b)
866 (c) There are 16 P − O bonds in P4 O10.
In structure (c), all the atoms have complete octet. 876 (a)
Thus, it is the correct representation of carbon Difference of electronegativity > 1.7 produces
suboxide ionic compound.
867 (b) 877 (a)
Smaller is atom, more is energy needed to remove It is a concept.
electron, 𝑖. 𝑒., ionisation energy. Also removal of 878 (a)
two electrons needs more energy. Low ionisation potential indicates that element
868 (d) can easily lose electron to form cation.
Born-Haber cycle inter-relates the various energy 879 (d)
terms involved in ionic bonding. Ionic compounds having lattice energy higher
869 (a) than hydration energy are insoluble in water.
BF3 (𝑠𝑝2 ), NO− 2 − 3 3 880 (a)
2 (𝑠𝑝 ), NH2 (𝑠𝑝 )and H2 O(𝑠𝑝 ).
870 (c) Removal of electron is easier in 𝑓-block elements
𝑠𝑝3 hybridisation Tetrahedron due to more shielding.
molecule 881 (d)
𝑑𝑠𝑝2 hybridisation Square planar Metals and non-metals combine to complete their
molecule octet. Since, non-metals have lack of electrons, in
𝑠𝑝3 𝑑 hybridisation Trigonal order to complete their octet, they gain electrons,
bipyramidal molecule consequently, the size of non-metal atom will
𝑠𝑝3 𝑑2 or𝑑2 𝑠𝑝3 Octahedron increase.
molecule Metal + Non − metal ⟶ Electrovalent bond
hybridisation (Na+ )(Cl) NaCl
871 (b) 882 (d)
These are characteristics of hydration.
883 (c)
Molecules or ion having no unpaired electrons are
diamagnetic, 𝑒. 𝑔.,
Total number of unshared electrons = 4 × 4 = 16 Li2 = 6𝑒 − = 𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2
872 (d) 884 (a)
Ionisation energy order is B < 𝐶 < 𝑂 < 𝑁. Given electronic configuration of anion X is
873 (d) 𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜋2𝑝𝑥2
Given, = 𝜋2𝑝𝑦2 , 𝜎2𝑝𝑧2 , ∗𝜋 2𝑝𝑥1
observed dipole moment = 1.03 D ∴ Total number of electrons of anion X = 15
Bond length of HCl molecule, d = 1.275 Å Hence, the anion Xis N2− .
= 1.275 × 10−8 cm 885 (a)
− −10
Charge of electron, 𝑒 = 4.8 × 10 esu Small cation causes more polarization in anion.
Percentage ionic character = ? Also larger anions are easily polarized by a cation.
Theoretical value of dipole moment = 𝑒 × 𝑑 More is polarization of anion, more is covalent
= 4.8 × 10−10 × 1.275 × 10−8esu.cm character.
= 6.12 × 10−18esu.cm 886 (c)
= 6.12 D Hydrogen bonding is responsible for their
solubility. 𝜋2𝑝𝑦2 ), ( ∗𝜋 2𝑝𝑥1 = ∗𝜋 2𝑝𝑦1 )
887 (a) ∵ O2 molecule has unpaired electrons.
Nehas van der Waals radius larger than covalent ∴ O2 molecule is paramagnetic.
radius of fluorine. 901 (c)
888 (c) C2 , N2 andF2 has no unpaired electron in their
As the number of unpaired electrons (lone pair of molecular orbital configuration.
electrons) increases, bond angle decreases. Thus, 902 (d)
the decreasing order of bond angle is IPof inert gases is maximum.
Species :NO+ 2 > 𝑁O2 > NO2
−
903 (d)
Bond angle: 180° 135° 115° Culoses two electron to form Cu2+ .
889 (a) 905 (a)
Dipole moment of CH4 = 0. O+ −
2 (15 𝑒 )
890 (b) 2
= 𝐾𝐾 ∗ (𝜎2𝑠)2 ( ∗ 2 2
𝜎 2𝑠) (𝜎2𝑝𝑥 ) , (𝜋2𝑝𝑦 )
Each has 22 electrons. 1
891 (d) = (𝜋2𝑝𝑧 )2 ( ∗𝜋 2𝑝𝑦 ) = ( ∗𝜋 2𝑝𝑧 )0
1
CS2is linear having zero dipole moment. Hence, bond order = 2 (10 − 5) = 2.5
892 (a) 2
N2+ (13 𝑒 − ) = 𝐾𝐾 ∗ (𝜎2𝑠)2 ( ∗𝜎 2𝑠)2 (𝜋2𝑝𝑦 )
Atomic radius decreases along the period,
= (𝜋2𝑝𝑧 )2 , (𝜎2𝑝𝑥 )1
increases down the group. 1
894 (b) Hence, Bond order = 2 (9 − 4) = 2.5
In NH3 , the N atom contains a one lone pair of 906 (b)
electrons and three bond pairs in its valence shell. In XeF5+ , Xe atom has only seven electrons ,𝑖. 𝑒.,
So, it shows 𝑠𝑝3 hybridisation. Due to presence of 5𝑠 2 5𝑝5. Here two 5p electrons are promoted to
one lone pair of electron, its shape deviates from 5d-sublevel. Then 5s, three 5p and two 5dorbitals
tetrahedral because lone pair shows more hybridize to give six 𝑠𝑝3 𝑑2 hybrid orbitals in an
repulsion than bond pairs. octahedral geometry. Out of these five orbitals are
As singly occupied which form sigma bonds with five
𝑙𝑝 – 𝑙𝑝 > 𝑙𝑝 − 𝑏𝑝 > 𝑏𝑝 − 𝑏𝑝 F atoms. The sixth hybrid orbital is occupied by a
So, its shape is pyramidal and angle 107°. lone pair in 𝑡𝑟𝑎𝑛𝑠 position giving a square
895 (d) pyramid structure.
The 𝐾𝑠𝑝 value of CuS is less than ZnS and thus, ZnS 907 (d)
is more soluble. Also sodium salts are highly HOMO, means highest occupied molecular orbital
soluble in water. and in CO (14 electron ion ),𝜎 bonding molecular
896 (c) orbital in HOMO
Both carbon atoms have 2σ-and 2π-bonds. CO = 𝜎1𝑠 2 , 𝜎 ∗ 1𝑠 2 , 𝜎2𝑠 2 , 𝜎 ∗ 2𝑠 2 , 𝜋2𝑝𝑥2
897 (b) = 𝜋2𝑝𝑦2 , 𝜎2𝑝𝓏2
1debye = 10−18 esu. 909 (c)
898 (c) Sulphur is 𝑠𝑝2 hybridised in SO2 .
Low ionisation energy indicates that electron can 𝑆 = 1𝑠 2 , 2𝑠 2 2𝑝6 , 3𝑠 2 3𝑝4 3𝑑0
be easily lost and cation formation is easier.
899 (b)
The paramagnetic species has unpaired electron
in it.
(a)H2 = 1 + 1 = 𝜎1𝑠 2
(b)N2 = 7 + 7 = 14 =
Due to 𝑠𝑝2 -hybridisation and presence of one lone
𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜋2𝑝𝑥2 = 𝜋2𝑝𝑦2 , 𝜎2𝑝𝑧2
pair of electronsSO2 has angular geometry.
(c)CO = 6 + 8 = 14 =
𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜋2𝑝𝑥2 = 𝜋2𝑝𝑦2 , 𝜎2𝑝𝑧2
(d)O2 = 8 + 8 = 16 =
Among N2 O, CO2 and CO, all have 𝑠𝑝-
𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜎2𝑝𝑧2 , (𝜋2𝑝𝑥2 =
hybridisation.
910 (c) The three fluoride atoms lie at the corners of an
Coordinate bonding involves sharing of an equilateral triangle with boron at the centre.
electron pair provided by a donor to acceptor Thus, the vectorial addition of the dipole
atom. moments of the three bonds gives a net sum of
911 (a) zero.
In the structure of P4 O10 , each phosphorus atom is
covalently linked with three oxygen atoms and
each oxygen atom is bonded to two phosphorus
atoms. Each phosphorus atom is also linked with
an additional oxygen atom with the help of a 920 (c)
coordinate linkage by lone pair of electron Bond order ∝ Stability
present on P atom. Hence, for a stable molecule the value of bond
order must be positive. When bond order is zero
the molecule will not exist.
921 (b)
Follow Fajans’ rule.
922 (b)
It is a fact.
923 (a)
In PCl3 and POCl3 , P atom is 𝑠𝑝3 -hybridized.
924 (c)
Square planar geometry has 𝑑𝑠𝑝2 -hybridisation.
925 (c)
Both BrO− 3
3 and XeO3 have 𝑠𝑝 -hybridisation and
912 (d)
one lone pair of electron.
H2 C = C = CH2 or
926 (a)
Allene(C3 H4 )
HF and CH3 OH shows intermolecular hydrogen
HH
bonding.
||
927 (d)
H−C=C=C−H
During hydration of ions in aqueous solution,
It has 2 double and 4 single bonds
there exists an attractive force between ions and
913 (b)
water molecules, which are polar in nature and
CsClis ionic.
acts as dipole. So, hydrogen of ions in aqueous
914 (c)
solution is an example ion-dipole interaction.
In NaOH, Na+andOH − ions are bonded together
928 (c)
by ionic bond while in OH − ion oxygen and
According to Fajan’s rule, largest cation and
hydrogen atoms are bonded together by covalent
smallest ions form ionic bond
bond Na+ [O − H]− .
929 (d)
915 (d)
Phosphorus atom is 𝑠𝑝3 hybridised in 𝑃4 usually.
Effective nuclear charge increases in this order.
Therefore, p-character 75%
917 (d)
930 (c)
AgBrhas higher lattice energy.
Na+is cation; Cl− , PO3−
4 are anion.
918 (c)
931 (c)
74 198
rH = = 37pm, rCl = = 99pm. Ionisation energy decreases down the group.
2 2
B.L. of HCl ≈ rH + rCl 932 (d)
919 (b) The characteristics to be observed during removal
A symmetrical molecule have zero dipole of II electron.
moment. The dipole moment of BF3 molecule is 933 (c)
zero due to its symmetrical (triangular planar) 1.(N2 ⟶ (σ1𝑠)2 (∗σ 1𝑠)2 (σ2𝑠)2 ( ∗σ 2𝑠)2
structure.
(σ2𝑝𝑧 )2 (π2𝑝𝑥 )2 (π2𝑝𝑦 )2
N2+ ⟶ (𝜎1𝑠)2 (∗𝜎 1𝑠)2 (𝜎2𝑠)2 ( ∗
𝜎 2𝑠)
2
PCl5 = 𝑠𝑝3 𝑑(Trigonal pyramidal)
IF7 = 𝑠𝑝3 𝑑3 (Pentagonal bipyramidal)
(𝜎2𝑝𝑧 )2 (𝜋2𝑝𝑥 )2 (𝜋2𝑝𝑦 )1 H3 O+ = 𝑠𝑝3 (Pyramidal)
ClO2 = 𝑠𝑝2 (Angular)bond length are shorter than
1.𝑂2 ⟶ (𝜎1𝑠)2 (∗𝜎 1𝑠)2 (𝜎2𝑠)2 ( ∗
𝜎 2𝑠)
2
(𝜎2𝑝𝑧 )2
single bond due to resonance.
(𝜎2𝑝𝑥 )2 (𝜎2𝑝𝑦 )2 ( ∗
2𝑝𝑥 )1 ( ∗
2𝑝𝑦 )
1 NH4+ = 𝑠𝑝3 (Tetrahedral)
𝜋 𝜋
O+ 2 ∗ 2 2
2 ⟶ (𝜎1𝑠) (𝜎 1𝑠) (𝜎2𝑠) (
∗
𝜎 2𝑠)
2
(2𝑝𝑧 )2
946 (d)
2
(𝜋2𝑝𝑥 ) (𝜋2𝑝𝑦 ) 2( ∗
𝜋 2𝑝𝑥 )1 B in BF3 has 𝑠𝑝2 -hybridization.
947 (c)
Since , 𝜋2𝑝𝑥 and 𝜋2𝑝𝑦 are nearly same in energy, In metallic bonds, the valence shell electrons are
delocalised and shared between many atoms.
the electrons can be removed from (𝜋2𝑝𝑦 or 𝜋2𝑝𝑥 )
These delocalised electrons allow the metal atoms
∗ ∗ to slide past one another without being subjected
and ( 𝜋2𝑝𝑦 or𝜋2𝑝𝑥 ) respectively.
strong repulsive forces. The malleability and
934 (b) ductility of metals is due to this sliding capacity of
Both possess 1𝑠 2 , 2𝑠 2 2𝑝6 , 3𝑠 2 3𝑝6 configuration. the delocalised electrons.
936 (d) 948 (b)
The resultant dipole in regular tetrahedron is CH3 − CH2 − NH2
zero. 𝑠𝑝3 𝑠𝑝3
937 (c) CH3 − CH = CH2
Smaller the size of cation, more is ionic character, 𝑠𝑝3 𝑠𝑝2 𝑠𝑝2
more is attraction among ions. O
938 (c) ||
Given ionic charge = 4.8 × 10−10 e.s.u. and ionic CH3 − C − NH2
distance = 1Å = 10−8 cm. We know that dipole 𝑠𝑝3 𝑠𝑝3
moment = Ionic charge × ionic distance CH3 − CH2 − C ≡ N
= (4.8 × 10−10 ) × 10−8 𝑠𝑝3 𝑠𝑝2 𝑠𝑝
= 4.8 × 10−18 e. s. u. per cm 949 (a)
= 4.8debye. A reason for given fact.
939 (d) 950 (c)
As the 𝑠-character increases in hybridised
orbitals, its electronegativity increases.
𝑠𝑝𝑠𝑝2 𝑠𝑝3
𝑠-character 50% 33.3% 25%
940 (d)
PCl3 andAsCl3 have 𝑠𝑝3 hybridisation and PF5 has
𝑠𝑝3 𝑑 hybridisation. Hence, in group of PCl3 , AsCl3
and PF5 all do not have 𝑠𝑝3 𝑑 hybridisation. Benzene nitrile contains 13σ and 5π bonds.
942 (d) 951 (d)
Each has 18 electrons. During melting of SiO2 , the gient network
943 (b) structure held by covalent bonds breaks to give
Alkali metals are always univalent. individual molecules ofSiO2 . In contrast, during
944 (c) boiling of H2 O only change of state occurs from
XeF4 has𝑠𝑝3 𝑑2-hybridized Xe atom having two liquid to gaseous; during melting of KCN,
lone pair of electrons and thus, octahedral electrostatic attraction between K + and CN − ions
geometry changes to square planar due to lone is overcome ; during boiling of CF4 , van der Waals’
pair effect. forces of attraction breaks
945 (d) 952 (b)
Ethyl alcohol C2 H5 OH is soluble in water due to H- Valency +3 -2
bonding. Therefore, Al3 (SO4 )3 is compound of Al3+
andSO2− 4 .
On comparing, x=2
Hence, formula of potash alum is
= K 2 SO4 . Al2 (SO4 )3 . 24H2 O
964 (d)
For KO2 , O− 2 has unpaired electron so, it is
953 (b)
paramagnetic.
Only 𝑝-orbitals give rise to σ-bond (head on
O−2 (17)
overlapping) and π-bond (lateral overlapping).
𝜎1𝑠 2 , ∗𝜎 1𝑠 2 , 𝜎2𝑠 2 , ∗𝜎 2𝑠 2 , 𝜎2𝑝𝑥2 , (𝜎2𝑝𝑦2 = 𝜎2𝑝𝑧2 ),
954 (b)
∗ 2 ∗ 1
HClandAlCl3 are covalent but give ions in solution. 𝜋 2𝑝𝑦 = 𝜋 2𝑝𝑧
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