Anloes_ 0 Benzene lo m- nitro benzaldehyde ») Bromoetane to Propanamine, 3) Flhaneie add le — metharamére 4. Fane nitrile bo ethomamt re. 5s pnicine fe phenol ge Renswie ad fo anttine y pring fo p- brome aritine g pritine fy Sulphanidic eA. 9, rithalimide Co Ethamaméne. jo pnilire to phenyl bowantda ek Qrtre .be mettyt 0 thio anate » pe. pine fe Paya Iycbrory atoben tere 13. priktre fo ben zantlide - WA. prifine bo Sechipf's dase is. wylle am Bones 0f Callgn Which Gives foul 8mes/- Of woyorncde when Bealood wit! CAtl, ond ethancdtic NaH (b- Distingush 2) (Cs) anh G0 (CHa) sn 1) Colts Na amd CHa Nie ™ eyscH2 Ne ard (Els Hs),ani whale Hinsherg's reagent, write its Use why = pe Qméires bemvoe as nudeoplsites Alucne €2 2-bromob@nzole aun, (Te 18+ 19 fava mo 20. out of —fulan-l-0d and Luten-\- Amine, which wil be move Solu in vabet al why? 21 W) --. apitine oes pet reat wits metiyt chJorids. in fhe presente. OF anbydrous plils lpevzene diazonium chloride nitro berrene eS why acebjatiog of <> Anktine reduces ils achvabjon epect. 2 te fo ne phenhetbanamble. 25 write the dleminl reactor mellyl amére wth berryl Werita and write Yho juppe Dome & the roauct obtained 26. why amilire aupot be prepared by Ue amroretysis wy chlow benzene under ermal Condifon,oy why yn. ellyl benzene sulphonyf amele 13 Soluble SL in atratt 2g Reduction & Dito benzene Using Fe and Het preferred OVE 97 amd HCL 6D. values 52 K 9 pecreasing oid GF PS 2 ar Wie » Ugnla Nia Gols, CllsNUChs, ONE M2 30 Pmmonoiysis of kyl halides js Rob @ geod method fo Prepare pure primary amines b3 3) Priline on achkatlan GES Good amit of m- ritoantcrea , fhorgh-~ Ng Frege bs YP dre: bres in ebetrophitic Substitaljop veact/ors ©3 32 Why aniwee woes tot Ceretergo Pvede - ctafls ee 33 Prange the jnereasing order of thety LotLing 2 “* CoHGOU , CaWs My, (Gus s~ Z | an Compared Be Jyring pateah Lreabment with om eleadlay rrila rr OM), on 0 B42 aol KOH GIVES” B’ Ce, wy. ett on obazotimban gives C. 0 ve with yN) Lehiche Solon Y then coat forme De co eb kx Gives £, Teenthly AE. wrike chemical wectiny jovetved 3s Ge %E2622, Anidine js a Weakey base Teen Cydloheryt arine 34, promatie dioxontum gl, Gre more stelle Gan Aabphatie raxonium Sak, By . genie pribelé ove gyptleses i pol preferred fot preparing ~ gromatic” —priraay Qari na thar tytlohexy samtne ag Initine jy tess basse nallybynine in water reals with Fetls fo precipitate * Iydiabel semic oxi. jv why pyridine je sed 19 the acylation veactior of amines gy increasing Order Of fasie strergths Collis hata , CHEN Chg iCo¥gNN2 4 an nee or”. ay, oats 12 why aliphabic amines are stroqger base than ammonia. 43 Describe a metbed for tha Sepasation [42 ani 4 amine. pir wrike chemical paleo foe Tookeig SovitiasyNez Wn el felUef p Nonozancl, pg Cischzol. 273K ns Clg0N lo cds CHy CNOl more ean two slap) 8 EN 4aly yg cide +koy 4b CHgcl > A ow ‘log t ar » Ll Be? "Hepes ta? 2 ch iS Nv. a jli 72 ® - 48 Coll N2BF NaNba/ue 4 pe foeh, g castot/ Pit a 4 ae A 49 Gos Comig BY ey, Kon! A nanos+ Hes B Bie [tise , eee! gH oe Sv Cola NH, Ltstock ConSN cucls +Kow 3+ Ha SOy / D> Chgl0) 20 5) Gla Nis» Gue-conm, S724 Naoy 8 (erste) 20 A }é n Hithty J ethey "2 Cay) es D S52. CH3¢o Ng Bufate Kort, A crecout B Hs 53 Toluene yp pohuidine. oy, P- Coluidine déaronium chloride ~~ P- tobut ay 2 elscispe EN —> p 10U4 5 g non ee aa A Neots Fe) g ae + Alekoy, wud _a7ak B S17, ple < oo on Ma Po A heat, AS: Conh: * (043 2) 5.0 [esis a ! 58. Bro Jaen. Col _Bro/uaon, 45 A huphocanbop AC C445) on vecttion wit hel Jives a compound B COyNgh) Which on Teathay ov yeachon with — | rede of Nis JVES Compound C Lest). On Yeacking with NANO2 Arl Het C Low bem perature followed Ay beeatment! aa waler compoird ‘oc! yields opliedlly active akechodés). Ozrolysis of 9’ gives 2 Moles Cf atelallehyde. Jdecbity te Compounts ~ lo D. 6° N. elfylethanamine bo/t, al 329-3K and butanamine bolts al 25008K, abthagh 40 ave Isoneeric jn Pot. Frepdadn /. 62. Bromoetlame fp Propamamire Pn OVGanic Conpoun) 9? with redecaloy formuta Cy 4pNo ‘eacks With Bog. Kon fe Give compoury B. Which Luypon Yeaction. With NaNO. ancl Hel at oc INCE ‘Cc’ | Compound “c’ on Aeatip 0B hecroy gives a lydrocarbon ‘D. Compouml B on putter Neachian Wi Bry water GNes while precipitade wy Comgpoual blentity Ar Bc Dar F, 63 chleroetlare te methanamire. b4. Coxbytamine test 65. Gabries phttaliméile Yn thesis