° t cH, om on a wo of Wocare of (1) 8 (2) Om, 2 BPE geenrescion e ow me 2 ofa EEE Product (Mayor) Om, ‘The proc it De [ Ce2ouene gh Trone-2tene @ zeae (4) Buta-1, 3dene Zi Grow Gertcal conditions, solvolysis of which of the teioemng substrate would lead to maximum cemeaton? cH, cH, : Br oto gf & OCH, oH, Br a &+{0)-n0,) cen—t-o K cH, 1 cna vi wn Br IS gan aceon 24. When cis-but-2-ene ts tested with Br, CC, Haloakanes ond Hatcarenes (aT SST ‘the product formed wit be, LAY ER. 38) corona tare Previous Years Questions dently A and predict the type of reacson OCH, fet a. ‘Br OCH, a er and substitution reaction NH, @ and elimination addition reacson (NEET2017] Consider the reaction CH,CH,CH,Br + NaCN > CH,CH,CH,CN + NaBr This reaction will be the fastest in [NEET4Phase-Z}2016} (1) Ethanot ) Methanol @)_N,N’dimethytiormamide (OMF) (4) Water ‘Wieweh Peer openat @oi-ae | jenited : Read Office -Askash Tower, 8, Pusa Road, New Defhé-110005 Ph 011-47623456"& t 4 P 2 ane oD O's e Fee genes sepals FOF, CHON COOH, ace eee, oe oni ReAIPMT 2015] D Branewres @) Mesomens eD Dererrevners (@) Atopromen: Ran Scr master on china! conten, ere te {Re-AIPM T2018) RON ent @_ HEX dresser WON renee 6) rresninn mare han retonton lating 10 partial RM WHED oF Pe Kolowny Aompounda, the C = CF Re Kontanon shall give MOST SADIE CaroNUM ~~ TAIPMT-2015) @ MCN * Ns Soe Nie ner ry aanee* 7 " So Sono D mo? ow) wnse gradtucts are Formed when the following Wh. Renaeh Tamaronsl Rervices Vented: ry Read. Oitice Aakash Tower, 8. Pusa Road, New Deihict 10008 Ph 011-476 ag My er OL,,,, and ° ym , 8 Which of the following compounds wit un, racamisation when solution of KOH hydrate, © on (0 croHoya on bad (wy no-ccnct — ™ H“Eea (arpa (1) (Menai) 2), (i)and tw) @) (iyana cv) * (4) Menai Inthe replacement reaction Cl+ MF =>) CF + MI The reaction will be most favourable if M haope tobe [AIPMT (Mains)20¢ (1) Na @K AY RD “Wt (4) ui 10. Which of the following compounds under nucleophilic substitution reaction most easily? [AIPMT (Mains}20" coy ” Q " @ . 2 cl Cr, . oO 0D CH,greater re FeRCtONS yy consiterthe fACH “CHEF _ SA 4 (CH), CH-CHOC,H, * HBF @ CAYO S884 (CH), CH-CH,0C,H, * BE me mechanisms of reactions (i) and (i) sre ey TAIPMT (Maires)-2011} om S2endS2 @ SZandst em Stare 2 (4) S,tend St ag. The correct order of increasing reactivity of CO tore marc nucteophve in the folowing « x a =o) Oo nO, a mayc-x IV. (CH,CH-X IAIPMT (Prelims)-2010] quicncves @ u one product : (4) S,1 gives one product but 8,2 gives two @ sho omed cH, 24 In Fiemetstein reaction when acetone is replaced by water ten cH, (1) Reaction occurs in forward direction via S, bak, Panay @) t Br @} Reaction occurs in forward direction via &,2 oH 4 49) Reacton occure in backward because NaCI | formed in night hand side is soluble in water 4 a 2d cannot pot out NW {oh CH CH, (4) Reaction is rot posstie Br (Aenean Educational Services Limmed | Regd. Office -Autash Tower # Pic.p..,.we S_____ttaoaanes a Haoarenes St © peerereeseeesen eminem (1) trans-pentene-2 (2) Pentene-1 @) 2-ethoxypentane (4) cls-pentene-2 34. Which of the following compounds is not chiral? (1) CH,CHDCH,CI @) CH,CH,CHOG @) DCH,CH,CH,Cl (4) CH,CHCICH,D 38. Anorganic compound A(C,H,C!) on reaction with Nal diethy! ether gives @ hydrocarbon which on ‘monochlorination gives only one chloro derivative then, Ais (1) Houtyl chloride (2) Secondary buty! chloride @) Isobuty! chloride (4) mbuty! chionde . “reer yg. Reacvty order othalids for dehydrohalogenatons moe @ eo (1) R=F>R-CI>R-Br>R=1 owe ) For @ R-1>R-Br>R-Cl>R-F 38 When CH.CM,CHCI, # Peated with NaNH,, the @ R-1>R-Cl>R-Br>R-F prokact DOTS my -cHAO () R-F>R-1>R-Br>R-Cl mm O-CHOt a7. cHcH i Me x ny Ne, in the above reacting sequence is s moe, (1) CHCH,CHNHCOCH, Cl (2) CH,CH,CH,NH, 6 none (3) CH,CH,CH,CONHCH, 1 Gryrart agents prepared by the reacton between (4) CH,CH,CH,CONHCOCH, © agreun ord akare 38 Which of the following is least reactive in a @ Magresasm and aromatic hydrocarbon nucieophilic substitution reaction? OF Dre ond airy nate (1) (CHy,c-c8 & Magnesium and ay! habde (2) CH, = CHI Te talowing macton is described 3s @) CH,CH,A. Why (OA.CH, (4) CH, = CHCH,Ct a I 39. Which of the following is not chiral? vh \ (1) 2-hydroxypropanoic acid He cH, (2) 2-ditanot "82 @) 8,0 @) 2,3-dbromopentane as (4) 5,1 (4) S-bromopentane ‘Mt Levcatenal Serviced United 3 Regd OMhice -Aakach Tower, 8, Pisa Rood, New Deihi:110005 Ph. 011-47623456) Pee.pan ay “4 Rave ‘Aakash Ediscational Services Limited ; Regd. Office ( roe) (i) XA, es Answers : 287 < 2m 3 9. 6 HM 7 & ‘ 9 @ 10. (1) 42. (1) 13. (4) 14, (4) 6 18. @) 1. @) 19. (2) 20. (1) 21. 4) oo @ 24, 2% 1) 27. @) 28. @) a 30. @) 3. @) 33. (2) 34. 2) 35. 4) » @ 37. (2) 38. i) 40. (2) ASSIGNMENT geton A: Objective Type Questions 1 2 @ 3. @ 5. 4) 7 2 ® % @ 10. 2 12. @) @ 4. @) 5. 16. (2) 47. @) 49. (1) 4 21. 3) 2. 2. (1) 24. 2) 26. 4) a) 28. (3) a 30. (2) 31 @) 33. (4) 2 3. 2) 6 37. (4) 38. qa) 40. (2) @ 42. (2) “a 44. (1) 45, section B : Objective Type Questions 1. 2 3. 2 5. (2) 4) 7 6 8 an) 10. a 12. (a) ® 14. @) 1 (4) 16. (4) a7. a) 19. (2) @ 2. 2@ 2B @ 24, ® {action C : Previous Years Questions: 1 2 @ 3. (O} 5. (4) 6. @) 7 @) 8 2 @ 10. @) 12. (1) 13. 3) 14. 3) 8. 16. @) 1. ® 9 @ 2 tt) 2 23. @) 24. @ 26. (4) 27. (2) 28. (1) w 30. @) 3. «) 2 0) 6% BS %. 37. (2) 38. @) s Section D : Assertion-Reason Type Questions 1 2 @ 3 “ 5 @) 9» 7 @® 8 2 10. @) ® 12 @) o % @ 5.) Chapter 24 = Alcohols, Phenols and Ethers Ty Yourself Aakash Tower, 8, Pusa Road, New Dethi-110005. Ph.011-47623456)