Msc-Chemistry (Under CBCS) FIRST YEAR 2017-18 Two Semesters: 15 Weeks Each
Msc-Chemistry (Under CBCS) FIRST YEAR 2017-18 Two Semesters: 15 Weeks Each
(Under CBCS)
FIRST YEAR 2017-18
TWO SEMESTERS: 15 WEEKS EACH
TEACHING AND EXAMINATION SCHEME OF FIRST SEMESTER
CORE COURSE:
Spectroscopic Techniques-II
Inductively Coupled Plasma Spectroscopy (ICPS): ICP -AES, ICP-MS, OES,
Theory, instrumentation and applications. 15 HRS
Unit 3 Fluorescence Spectroscopy: Principle, Fluorescence, Phosphorescence basic
Instrumentation and their applications. Chemiluminscence.
Nephelometry and Turbidometry: Principle, instrumentation and applications.
Seperation Technique
Solvent extraction- Principle, methodology and applications, Synergistic
15 HRS
Unit 4 extraction: determination of nickel, crown ether for ion association complex.
Organic reagents like dithiol, diketones, oxinedithizone, cuproin, cupferron,
dimethylglyoxime and dithiocarbamates in solvent extraction and electrophoresis
Chromatography: Introduction.
HPLC: Theory, General layout of equipment, detector working principle (u.v
detector, luminescencedetector, refractive index detectors)and applications.
15 HRS
Unit 5 HPTLC:Principle, advantage over TLC, mobile and stationary Phase
Gas chromatography: Theory, General layout of equipment, detectors (Flame
ionization, Photoionization detector, coupled GC detector) and applications.
Gas Chromatography –Mass spectrometry
Suggested Readings:
1. Vogel's Textbook of Quantitative Chemical Analysis, G.H. Jeffery, J. Bassett, J. Mendham
and R.C. Denney, Publ ELBS, Longman, UK
2. Basic Concepts of Analytical Chemistry, S.M. Khopkar, Wiley Eastern.
3. Fundamentals of Analytical Chemistry, D.A. Skoog, D.M. West and F.J. Holler. Pubi WB
Saunders.
4. Analytical Chemistry, G.D. Christian, John Willy & Sons.
MSCH121-LABORATORY COURSE-I: INORGANIC CHEMISTRY
I. Qualitative Analysis: Qualitative estimation of the inorganic mixture for six radicals including
interfering acid radicals, their combinations and insoluble oxides, sulphates and halides
including rare earth elements.
II. Quantitative Analysis:
a. Separation and determination of two metal ions Cu-Ni, Ni-Zn, Cu-Ag etc, involving
volumetric and gravimetric methods.
b. Estimation of three constituent in the given mixture (one gravimetrically and
one volumetrically and one colorimetrically).
III. Chromatography
a. Separation of cations and anions by circular Paper Chromatography.
Suggested Readings:
THEORY:
Fundamentals of cosmetic science. Classification of cosmetics. Structure and function of skin
and hair. Formulation, preparation and packaging of cosmetics for lotion, suspension,
vanishing cream, paste, shaving cream, liquid detergent, ointment.
EXPERIMENTS: Topical Preparations
1. To prepare sunscreen calamine suspension.
2. To prepare and submit vanishing cream.
3. To To prepare and submit Calamine lotion
4. To prepare and submit Zinc Sulphate lotion.
5. To prepare and dispense zinc oxide paste.
6. To prepare and dispense shaving cream.
7. To prepare and dispense astringent lotion.
8. Prepare and submit liquid detergent.
9. To prepare and submit boric acid ointment.
SUGGESTED READING:
THEORY
Introduction, classification of dyes, general idea about the synthesis of different dye
intermediates and synthetic dyes (azoic, acidic, basic, disperse, mordent and
Sulphur dyes). Dyeing processes of acrylic fibers. Finishes to improve colour
fastness, effect of temperature on the dying process, pigment for textile colouration.
PRACTICAL
1. Preparation of methyl orange.
2. Preparation of malachite green.
3. Preparation of natural dye.
4. Effect of mordents and modifiers on the process of dying.(Alizarin red
using Fe+2 , Mg+2,Al+3, Cu+)
5. To study the interaction of natural dyes with different fibers.
6. To study the interaction of synthetic dyes with different fibers.
7. To study the optimum PH for dying cotton cellulose fabrics.
8. Testing of dyes.
9. Thin layer chromatography of dyes.
SUGGESTED READING:
THEORY PRACTICALS
CODE DESCRIPTION
HRS/W HRS/SEM HRS/W HRS/SEM
MSCHSC231 FUNDAMENTAL CONCEPT IN
CHEMICAL CALCULATIONS: 2 15 2 30
STOICHIOMETRY
STUDENT HAVE TO OPT ANY ONE OF SKILL BASED PAPER FROM SKILL
BASED PAPERS OFFERED BY OTHER DEPARTMENTS.
MSCH211-COORDINATION CHEMISTRY
Reaction mechanism of Transitions metal complexes
Energy profile of a reaction (transition state or activated complex) nucleophilic and
electrophilic substitution, factors responsible for types of substitution reaction.
Introductory classical reaction of Henry-Taube in octahedral complexes (inert and 15
Unit 1
labile complexes), classification of mechanism of. Acid hydrolysis, factor affecting HRS
acid hydrolysis, base hydrolysis, conjugate base mechanism (SN1CB) Evidences in
favour of conjugate base mechanism, anation reactions, Substitution reaction
without metal-ligand bond cleavage (Special reference to Co(III) complexes).
Substitution in square planer complexes:
Trans effect, mechanism of substitution reaction, polarization theory and π bonding
theory.
15
Redox reaction:
Unit 2 HRS
Classification of mechanism of octahedral complexes (inner and outer sphere
reaction; adjacent attack, remote attack. and bridged outer sphere reaction).
Electron transfer reaction, mechanism of one electron transfer reaction: outer sphere
reaction, Inner sphere reaction, bridge intermediate mechanism.
Isomerisation and Racemisation Reactions:
Linkage isomerization, geometrical isomerization in square planar and octahedral
complexes, racemisation: inter and intramolecular mechanism, isomerisation and 15
Unit 3 racemisation of tris chelates of unsymmetrical chelating ligands, structural changes HRS
in complexes containing terdentate ligands, optical isomerisation on tetrahedral
complexes and configurational changes in some planar complexes
Electronic spectra of Transition Metal Complexes
15
Spectroscopic ground states term, correlation, Orgel and Tanabe sugano diagrams
Unit 4 HRS
for transition metal complexes (d1 to d9 states) and calculation of Dq, B and β
parameters
Charge Transfer Spectra
General Introduction to charge transfer spectra and types of spectra.
Ligand to metal and metal to ligand charge transfer spectra of transition metal
15
complexes.
Unit 5 HRS
Magnetic Properties of Transition Metal Complexes: Anomalous magnetic
moments, magnetic exchange coupling and spin crossover.
ORD and CD: Introduction, assignment of absolute configuration in optically
active metal chelates and their configuration
Suggested Readings:
1. F.A. Cotton and Wilkinson: Advanced Inorganic Chemistry, John Wiley.
2. J.E. Huhey: Inorganic Chemistry, Harper and Row.
3. N.N.Green Wood and A. Earnshow: Chemisryof the element, Pergamon.
4. A.B.P. Lever: Inorganic Electronic Spectroscopy, Elsevier
5. R.L.Carlin: Magnetochemistry, Verlag.
6. G. Wilkinson, R.D. Gillars and J.A. McLeverty: Comprehensive Coordination Chemistry eds.
Pergamon.
7. F. Basolo and R.G. Pearson: Mechanism of Inorganic Reaction, Wiley Eastern.
8. D. Banerjia: Coordination Chemistry, Asian.
9. Advanced Inorganic Chemistry, Asim K Das
MSCH212-ORGANIC CHEMISTRY-II
Aliphatic Nucleophilic Substitution
The SN2, SN1, mixed SN1 and SN2 and SET mechanisms.
The neighbouring group mechanism, neighbouring group participation by π and
σ bonds, anchiomeric assistance.
Classical and nonclassical carbocations, phenonium ions, norbornyl system.
The SNi mechanism.
Nucleophilic substitution at an allylic, aliphatic trigonal and a vinlyic carbon.
Unit 1 15 HRS
Reactivity effects of substrate structure, attacking nucleophile, leaving group and
reaction medium, phase transfer catalysis and ultrasound, ambident nucleophile,
regioselectivity.
Aliphatic Electrophilic Substitution
Bimolecular mechanisms- SE2 . The SE1 mechanism, electrophilic substitution
accompanied by double bond shifts. Effect of substrates, leaving group and the
solvent polarity on the reactivity
Aromatic Electrophilic Substitution
The arenium ion mechanism, orientation and reactivity, energy profile diagrams.
The ortho/para ratio, ipso attack, orientation in mono and substituted ring
systems. Quantitative treatment of reactivity in substrates and electrophiles. 15 HRS
Unit 2 Diazonium coupling, Vilsmeir reaction, Gattermann-Koch reaction.
Aromatic NucleophilicSubstitution:TheSNAr SN1 benzyne and SRN1
mechanisms. Reactivity effect of substrate structure, leaving group and attacking
nucleophile. The von Richter, Sommelet-Hauser, and Smiles rearrangements.
Free Radical, Reactions:
Types of free radical reactions, free radical substitution mechanism, mechanism
at an aromatic substrate, neighbouring group assistance.
Reactivity for aliphatic and aromatic substrates. Reactivity in the attacking 15 HRS
Unit 3
radicals. The effect of solvents on reactivity.
Allylic halogenation (NBS), oxidation of aldehydes to carboxylic acids, auto-
oxidation, coupling of alkynes and arylation of aromatic compounds by
diazonium salts, Sandmeyer reaction and Hunsdiecker reaction
Addition to Carbon-Carbon Multiple Bonds:
Mechanistic and sterochemical aspects of addition reactions involving
electrophiles, nucleophiles and free radicals, regio- and chemoselectivity,
orientation and reactivity. Addition to cyclopropanering. Hydrogenation of
double and triple bonds, hydrogenation of aromatic rings.Hydroboration.
Michaelreaction. Sharpless asymmetric epoxidation.
Addition to Carbon-Hetero Multiple Bonds 15 HRS
Unit 4 Mechanism of metal hydride reduction of saturated and unsaturated carbonyl
compounds, acids, esters and nitrites. Addition of Grignard reagents, organozinc
and organolithium reagents to carbonyl and unsaturated carbonyl compounds.
Wittig reaction.
Mechanism of condensation reactions involving enolates Aldol, Knoevenagel,
Claisen, Mannish, Benzoin, Perkin and Stobbe reactions.
Hydrolysis of esters and amides, ammonolysis of esters
Elimination Reactions:
The E1, E2 and E1cB mechanisms and their spectrum, stereochemistry of E1 and
E2 reactions and elimination from cyclic compounds. Orientation of the double 15 HRS
Unit 5 bond. Reactivity effects of substrate structures, attacking base, the leaving group
and the medium.
Mechanism and orientation in pyrolytic elimination.
Suggested Readings:
1. Advanced Organic Chemistry-Reactions, Mechanism and Structure, Jerry March, John Wiley.
2. Advanced Organic Chemistry, F.A. Carey and R.J. Sundberg, Plenum.
3. A Guide Book to Mechanism in Organic Chemistry, Peter Sykes, Longman.
4. Structure and Mechanism in Organic Chemistry, C.K. Ingold, Cornell University Press.
5. Organic Chemistry, R.T. Morrison and R.N. Boyd, Prentice-Hall Modern Organic Reactions,
H.O. House, Benjamin.
6. Principles of Organic Synthesis, R.O.C. Norman and J.M. Coxon, Blackie Academic &
Professional.
7. Pericyclic Reactions, S.M. Mukherji, Macmillan, India.
8. Stereochemistry of Organic Compounds, D. Nasipuri, New Age International.
MSCH213-PHYSICALCHEMISTRY-II
Quantum Chemistry
Introduction to Exact Quantum Mechanical Results: The Schrodinger
Unit 1 equation and the postulates of quantum mechanics. Discussion of solutions of the 15 HRS
Schrodinger equation to some model systems viz., particle in 1 and 3-
dimensional box, the harmonic oscillator, the hydrogen atom.
Quantum Chemistry
Electronic Structure of Atoms: Russell-Saunders terms and coupling schemes,
spectral terms for pn configurations and dn configurations.
Magnetic effects: Perturbation theoryNormal and anomalous Zeeman effects 15 HRS
Unit 2 and Stark effect.
Molecular Orbital Theory: Huckel molecular orbital (HMO) theory of linear
conjugated systems, bond order and charge density calculations. Applications of
HMO to ethylene, allyl, butadiene and cyclobutadiene system.
Classical Thermodynamics
Partial molalproperties: Partial molar free energy - chemical potential, partial
molal volume and partial molal heat content. Gibbs Duhem equation, variation of 15 HRS
Unit 3 chemical potential with temperature and pressure, chemical potential for ideal gas.
Thermodynamic derivation of law of mass action. Concept of fugacity and determination
of fugacity. Thermodynamic derivation of phase rule, application of phase rule to three
component systems
Statistical Thermodynamics
Concepts of phase space, microstate and macrostate, Ensemble averaging,
Canonical, grand canonical and microcanonical ensembles, Maxwell-Boltzman
distribution law (using Lagrange's method of undetermined multipliers).
Partition functions translational, rotational, vibrational and electronic partition
15 HRS
Unit 4 functions, calculation of thermodynamic properties in terms of partition
functions- Energy, specific heat at constant volume and constant pressure,
entropy, work function, pressure Gibb's free energy and chemical potential.
Chemical equilibria and equilibrium constant in terms of partition functions,
Fermi-Dirac statistics distribution law and Bose-Einstein statistics distribution
law.
Non Equilibrium Thermodynamics
Thermodynamic criteria for non-equilibrium states, entropy production and
entropy flow, entropy balance equations for different irreversible processes (e.g.
15 HRS
Unit 5 heat flow, chemical reaction etc.) transformations of the generalized fluxes and
forces, non-equilibrium stationary states, phenomenological equations,
microscopic reversibility and Onsager's reciprocity relations, electrokinetic
phenomena, diffusion, electric conduction
Suggested Readings:
1. Physical Chemistry, P.W. Atkins, ELBS.
2. Introduction to Quantium Chemistry, A.K. Chandra, Tata McGraw Hill.
3. Quantum Chemistry, Ira N. Levine, Prentice Hall.
4. Coulson's Valence, R. McWeeny, ELBS.
5. Physical Chemistry, S. Glasston, Princeton, London.
6. Non Equilibrium Thermodynamics, Fitts, McGraw Hills, New York.
7. Fundamentals of Chemical Thermodynamics, E.N. Yeremin, Mir Publishers
MSCH214: ANALYTICAL CHEMISTRY-II
Thermal analysis:
TGA, DSC (differential scanning calorimetry), DTA (differential thermal
Unit 1 15 HRS
analysis): principle, methodology and application
Polarography
Polarography: Principles, classification of polarographic techniques, types of
polarographic currents, instrumentation, factors affecting polarographic wave, 15 HRS
Unit 3 pulse polarography, and differential pulse polarograph,square wave
polarography.Applications
Sensors
Ion Selective Electrode: Classification,Application
Sensors:Definition-Classification-Optical,Thermal,Electrochemical,Condution 15 HRS
Unit 5 sensors, Gas sensorsBiosensors:Introduction, Working of Glucose Biosensors
Suggested Readings:
Suggested Readings:
1. Practical Organic Chemistry, SP Bhutani & Aruna Chhikara, Ane Books India
2. Elementary Practical Organic Chemistry Part I & II, Arthur I Vogel, CBS
3. Advanced Practical Organic Chemistry, NK Vishnoi, Vikash Publication
Suggested Readings:
THEORY:
Atomic weight, molecular weight, empirical formulae and its determination ,the mole
concept:elementry problem ,problem based on equation: stoichiometry , equivalent weight and
chemical equivalence, concentration units and volumetric calculation.
Practical:
Numerical problem based on above concept.
Preparation of solution: primary and secondary standard.
Dilution of solutions.
Suggested Books:
(1) Modern approach to chemical calculation by R.C.Mukherjee,Bharti Bhavan P&D
(2)Stoichiometry by B.I.Bhatt and S.B.Thakore.
(3) Stoichiometry and process calculations: K.V.Narayanan and B.Laxmikutty
TEACHING AND EXAMINATION SCHEME
THIRD SEMESTERCORE COURSE:
2018-19
CODE DESCRIPTION PD/W PD/SEM EXAM CIA ESE TOTAL
MSCH311 ORGANIC SPECTROSCOPY 4 60 3 HRS 30 70 100
SOLID STATE, SURFACE 4 60 30 70
MSCH312 3 HRS 100
CHEMISTRY & CATALYSIS
ORGANOTRANSITION METAL 4 60 30 70
MSCH313 3 HRS 100
CHEMISTRY
ELECTIVE
4 60 30 70
MSCH314(A) ORGANIC SYNTHESIS-I 3 HRS 100
OR
4 60 30 70
MSCH314(B) MATERIAL CHEMISTRY 3 HRS 100
TOTAL THEORY
400
LABORATORY COURSE V: 30 70
MSCH322 9 135 12 HRS 100
INVESTIGATORY PROJECT
LABORATORY COURSE IX:
MSCH323 6 90 6 HRS 15 35 50
ORGANIC CHEMISTRY
GRAND TOTAL 550
Note:
1. A board of two examiners (one internal and one external) will be appointed for
conducting the examination of each laboratory course.
2. In practical exam one major and minor experiment will be allotted in each lab course.
3. In inorganic mixture student can consult book for basic radicals after reporting the
concern groups.
4. In organic mixture student can consult book for confirmatory test of the compounds
after reporting the initial physical properties, element detection, functional group &
melting/boiling point of the compound.
5. Practical Exam shall be conducted in two days where ever required (Hours).
Surface Chemistry-II
Solubilization of surfactants: Solubilization in aqueous media; locus of
solubilization, factors determining the extent of solubilization, effects of
solubilization 15 HRS
Unit 4
Detergency and surfactants: Mechanism of cleaning process, removal of
soil from substrate, suspension of soil in bath and prevention of redeposition, dry
cleaning, skin irritation, effect of water hardness and chemical structure of
surfactants and its detergency.
Phase Transfer catalysis& ultrasound: Definition and importance of
15 HRS
Unit 5 phase transfer catalysis, quaternary ammonium and phosphonium salts, crown
eathers and other crypatants. Use of ultrasound.
Suggested Readings:
1. Solid state chemistry and its applications, West A.R., Plenum.
2. Principles of solid state, Keer H.V., Wiley Eastern
3. Solid state chemistry, Chakrabarty D.K., New Wiley Eastern
4. Solid state chemistry: An introduction, Moore E., and Smart L., Chapman Hall, 1996
5. Crystallography made crystal clear: A guide for users of macromolecular models, Rhodes
G., Elsevier, 2006.
6. X-ray diffraction, Warren B., Dover Publications
7. Introduction to crystallography, Sands, D.E., Dover Publications.
8. Principles and practice of heterogenous catalysis, Thomas J.M. and Thomas M.J., John
Wiley
9. Concepts of modern catalysis and kinetics, Chorkendoff I.B. and Niemantsverdriet J.M.
10. Physical chemistry of surfaces, Adamson A.W., Wiley Interscience, 1997
11. Surfactants and interfacial phenomenon, Milton J. Rosen, wileyinterscience.
MSCH313: ORGANOTRANSITION METAL CHEMISTRY
Organotransition Metal Complex
Definition, Classification and nomenclature
Types of ligendsamd M-L bonding: - lone pair donor, pi bonding electron pair
Unit 1 donor, Hapticity, ambidentate ligands, 15 HRS
18 Electron rule: electron counting, ionic v/s covalent model, compliance and
violation of the rule oxidation state of the metal.
Basic reaction in organometallic chemistry
Oxidative addition, reductive elimination, insertion elimination, ligand
15 HRS
Unit 2 substitution nucleophilic and electrophilic addition and abstraction
Fluxional organometallic compound: Rate of rearrangement and study technique,
fluxional molecules of C. No. 4, 5, 6
Complex of sigma-bonded ligands
Preparation, structure bonding and reaction of alkyl and aryl transition metal
15 HRS
Unit 3 Complexes of pi-bonded ligands: -
Preparation, structure and reaction of alkenes cyclopentadienyl complexes,
arenas, carbonyl complexes
Metal cluster and metal-metal bond
Structures, Isolable analogy, synthesis
15 HRS
Unit 4 Catalysis: Basic terminology turn over, turnover number, turn over frequency,
Dehydrogenation of alkene, Hydroformylation, Monsanto process, Wacker
process, Alkene isomerization, Olefin metathesis
Applications of organometallic chemistry in organic synthesis
Heck reaction, Suzuki – miyaura reaction, Sonagashira reaction, Stille coupling,
15 HRS
Unit 5 Kumada coupling, Pauson – khand reaction, Ullmann reaction, Organo copper
compounds
Application in medicine, agriculture, industries
Suggested Readings
1. Principles and Application of Organotransition Metal Chemistry, J.P. Collman, L.S.
Hegsdus, J.R. Norton and R.G. Finke, University Science Books.
2. The Organometallic Chemistry of the Transition Metals, R.H. Crabtree, John, Wiley.
3. Metallo-organic Chemistry, A.J. Pearson, Wiley.
4. Organometallic Chemistry, R.C. Mehrotra and A. Singh, New Age International.
MSCH314(A): ORGANIC SYNTHESIS-I
Organometallic Reagents
Principle, preparations, properties and applications of the following in
organicsynthesis with mechanistic details.
Group I and II metal organic compounds
Unit 1 Li, Mg, Hg, Cd, Zn and Ce compounds. 15 HRS
Transition metals
Cu, Pd, Ni, Fe, Co, Rh, Cr and Ti compounds.
Other elements
S, Si and B compounds.
Oxidation
Introduction, Different oxidative processes.
Hydrocarbons- alkenes, aromatic rings, saturated C-H groups (activated
15 HRS
Unit 2 andunactivated).Alcohols, diols, aldehydes, ketones, ketals and carboxylic
acids.Amines, hydrazines, and sulphides.
Oxidations with ruthenium tetraoxide, iodobenzene diacetate and thallium
(III) nitrate.
Reduction
Introduction. Different reductive processes.
Hydrocarbons – alkanes, alkenes, alkynes and aromatic rings.
15 HRS
Unit 3 Carbonyl compounds – aldehydes, ketones, acids and their derivatives
Epoxides.Nitro, nitroso, azo and oxime groups.
Hydrogenolysis.
Rearrangements
General mechanistic considerations – nature of migration, migratory
aptitude, memory
15 HRS
Unit 4 effects. A detailed study of the following rearrangements:
Pinacol-pinacolone, Wagner-Meerwein, Demjanov, Benzil-Benzilic acid,
Favorskii,Arndt-Eistert synthesis, Neber, Beckmann, Hofmann, Curtius,
Schmidt, Baeyer-Villiger, Shapiro reaction.
Polycyclic Aromatic Compounds.
Napthelene,Phenanthrene, Anthracene: Introduction and aromaticity,
general methods for synthesis,reactions and spectroscopic properities
Synthesis of linear ortho-fused and Non- linear ortho fused polynuclear 15 HRS
Unit 5
hydrocarbons:
Napthacene,Benz[a] anthracene, Dibenz[a,j] anthracene,Chrysene, Picene
Synthesis of ortho and peri fused polynuclear hydrocarbons:
Pyrene,Corolene 20-methylcholanthrene and circumanthracene.
Books Suggested:
1. Modern Synthetic Reactions, H.O. House, W.A. Benjamin.
2. Somer Modern Methods of Organic Synthesis, W. Carruthers, Cambridge Univ.
Press.
3. Advanced Organic Chemistry, Reactions Mechanisms and Structure, J. March,
John Wiley.
4. Principles of Organic Synthesis, R.O.C. Norman and J.M. Coxon, Blackie
Academic & Professional.
5. Advanced Organic Chemistry Part B. F.A. Carey and R.J. Sundberg, PlenumPress.
6. Rodd’s Chemistry of Carbon Compounds, Ed. S. Coffey, Elsevier.
MSCH314(B): MATERIAL CHEMISTRY
Multiphase Material :
Composite Materials:
Definition: composite, matrix materials: polymer, metal, ceramic and
glass matrix.
Unit 2 15 HRS
Reinforcement: dispersion reinforcement, partical reforcement, laminated
reinforcement and fiber reinforcement.
Natural and traditional composites (concrete, asphalt, wood)
Unit 5 Ceramic surfaces: Oxide ceramic surface, Nonoxide ceramic fiber 15 HRS
surface.
Suggested Readings:
1. Solid State Physics, NW Ashcroft and ND Mermin, Saunders College.
2. Handbook of Liquid Crystals, Kelker and Hatz, ChemieVerlag
3. Nanostructures materials: Processing, Properties and applications, C. C. Kouch,
William Andrew publications, New York, 2002.
4. Fundamentals of Materials science and Engineering. William D. Callister, Jr, Jhon
Wiley and Sons, Inc.
5. Introduction to Material Chemistry, Harry R. Allcock, Wiley and Sons, Inc.
MSCH321: INVESTIGATORY PROJECT
Student had to carry out an investigatory project under the guidance of the alloted guide and
submit the dissertation of the same at end of the semester.
Viva voce examination and presentation of the project will be held during the practical
examination.
Marking Scheme for the Project:
CCA : 30 Marks (Including 10 marks of the attendance)
Project Report (Dissertation): 35 Marks
Presentation : 15 Marks
Viva Voce : 20 Marks
MSCH322: LABORATORY COURSE VI: ORGANIC CHEMISTRY
I. Separation, purification and identification of the components of a
mixture of three organic compounds (three solids or two liquids and one solid, two
solids and one liquid).
II. Extraction of Organic Compounds from Natural Sources (purity of
isolated compound may be checked by chemical test TLC or Paper
chromatography):
a. Isolation of cafeine from tea leaves.
b. Isolation of casein from milk.
c. Isolation of lactose from milk.
d. Isolation of lycopene from tomatoes.
III. Interpretation of IR NMR and Mass Spectra of Organic Compounds.
Suggested Readings:
THEORY:
Fundamentals of cosmetic science. Classification of cosmetics. Structure and function of skin
and hair. Formulation, preparation and packaging of cosmetics gargle, mouthwash, throat
paint, mouth freshener, Astringent lotion.
PRACTICAL:
1. To prepare mouthwash.
2. To prepare and dispense effervescent granules.
3. To prepare and dispense potassium chlorate gargle.
4. To prepare and dispense saline mouthwash.
5. To prepare and dispense throat paint.
6. To prepare and dispense mentho-eucalyptus mouth freshener
7. To prepare and dispense Hydrogen peroxide mouth wash (6 % w/w).
8. To prepare and submit Astringent lotion.
Suggested Reading:
THEORY:
Introduction, types of milk, general composition of milk, physical and microscopic properties
of milk (fat globules, cellular element, refraction, gravity, conductivity, capillary
phenomenon and curd tension)
Milk products- pasteurized milk, artificial milk condensed milk, milk powder, cream butter,
ghee, cheese.
PRACTICAL:
OR
4 60 30 70
MSCH414(B) NANOSCIENCE 3 HRS 100
TOTAL THEORY
400
Note:
1. A board of two examiners (one internal and one external) will be appointed for
conducting the examination of each laboratory course.
2. In practical exam one major and minor experiment will be allotted in each lab course.
3. In inorganic mixture student can consult book for basic radicals after reporting the
concern groups.
4. In organic mixture student can consult book for confirmatory test of the compounds
after reporting the initial physical properties, element detection, functional group &
melting/boiling point of the compound.
5. Practical Exam shall be conducted in two days where ever required (Hours).
Suggested Readings:
A. Chemical Kinetics
a. To investigate the kineticsof the reaction between I- and persulphate ion
i. Order of the reaction
ii. Energy of activation of the reaction.
iii. Effect of ionic strength on rate.
b. To find out the order of the reaction of saponification of ester using unequal
concentrations of reactants.
c. To study the reaction between ceric ammonium nitrate and primary alcohol.
B. Conductometry:
a. To find out the equivalent conductance of strong electrolytes at different dilutions
and to verify Debye HuckelOnsagar equation.
b. To determine the equivalent conductance of a weak electrolyte at infinite dilution.
To determine the dissociation constant of acetic acid/Oxalic acid and verify the
Ostwald's dilution law.
c. Determination of the velocity constant, order of the reaction and energy of
activation for saponification of ethyl acetate by NaOHconductometrically.
C. Phase Equilibrium:
a. To find out the equilibrium constant for the triiodide formation.
b. To find the formula of complex cuprmmonium ion by distribution method.
c. To contracture the phase diagram for three component system (e.g.
Chloroform acetic acid-water)
D. Polarimetry
a. To determine the specific rotation of a given optically active compound.
Suggested Readings:
1. Practical Physical Chemistry, A.M. James and F. E. Prichard, Longman.
2. Findley's Practical Physical Chemistry, B.P. Levitt, Longman. Experimental Physical
Chemistry, R.C. Das and B. Behera, Tata McGraw Hill.
3. Advanced Practical Physical Chemistry, J.B. Yadav, Goel Publishing House.
4. Advanced Experimental Chemistry, vol.1, Physical J.N. Gurtu and R. Kapoor, S. Chand & Co.
I. Preparations
a. Na3[Fe(C2O4)3]
b. Prussian Blue( Fe4[Fe(CN)6])
c. [Ni(NH3)6] Cl2
d. [Ni(dmg)2]
e. Potassium Chlorochromate
f. Na3[Co(NO2)6]
g. K3[Cr(C2O4)3].3H2O
h. Cis& trans potassium diaquodioxalatochromate(III)
i. Potassium trioxalatochromate(III).
j. Cuprous tetraiodomercurate(II).
k. Tetraamminecarbonatocobalt(III) nitrate.
l. Pentaamminechloridocobalt(III) chloride.
m. Tris(acetylacetonato)manganese(III) ion
PRACTICALS:
Suggested Readings: