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MSCCH-02

December - Examination 2017

M.Sc. (Previous) Chemistry Examination Organic Chemistry

Paper - MSCCH-02

Time : 3 Hours ] [ Max. Marks :- 80

Note: The question paper is divided into three sections A, B and C.

Write answers as per the given instructions.

{ZX}e : ¶h àíZ nÌ "A', "~' Am¡a "g' VrZ IÊS>m| ‘| {d^m{OV h¡& à˶oH$

IÊS> Ho$ {ZX}emZwgma àíZm| Ho$ CÎma Xr{OE&

Section - A 8 × 2 = 16 (Very Short Answer Questions)

Note: Answer all questions. As per the nature of the question delimit your answer in one word, one sentence or maximum up to 30 words. Each question carries 2 marks.

IÊS> - "A' (A{V bKw CÎmar¶ àíZ)

{ZX}e : g^r àíZm| Ho$ CÎma Xr{OE& Amn AnZo CÎma H$mo àíZmZwgma EH$ eãX, EH$ dm³¶ ¶m A{YH$V‘ 30 eãXm| ‘| n[agr{‘V H$s{OE& à˶oH$ àíZ 2 A§H$m| H$m h¡&

1) (i) Define resonance.

AZwZmX H$mo n[a^m{fV H$s{OE&

209

MSCCH-02 / 900 / 4 (1) (P.T.O.)

(2)

209

MSCCH-02 / 900 / 4 (2) (Contd.)

(ii) What are crown - ether complexes?

H«$mD$Z B©Wa g§Hw$b {H$go H$hVo h¢?

(iii) What is fullerene?

’w$barZ {H$go H$hVo h¢?

(iv) Write the types of symmetry element present in a molecule.

AUw ‘§o {H$VZo g‘{‘Vr Ho$ VÎd nmE OmVo h¢ CZHo$ Zm‘ {b{IE&

(v) What is optical activity?

àH$m{eH$ g{H«$¶Vm {H$go H$hVo h¢?

(vi) Write a note on E1 elimination reactances.

E1{dbmonZ A{^{H«$¶m na {Q>ßnUr {b{I¶o&

(vii) Define conformation.

g§ê$nU H$mo n[a^m{fV H$s{OE&

(viii) What is Carbene?

H$m~uZ {H$go H$hVo h¢?

Section - B 4 × 8 = 32 (Short Answer Questions)

Note: Answer any four questions. Each answer should not exceed 200 words. Each question carries 8 marks.

IÊS> - ~ (bKw CÎmar¶ àíZ)

{ZX}e : {H$Ýht Mma àíZm| Ho$ CÎma Xr{OE& Amn AnZo CÎma H$mo A{YH$V‘

200 eãXm| ‘| n[agr{‘V H$s{OE& à˶oH$ àíZ 8 A§H$m| H$m h¡&

2) Give any four electrophilic substitution reactions of indole.

BÊS>mob H$s Mma Bbo³Q´>mo’$s{bH$ à{VñWmnZ A{^{H«$¶m {b{I¶o&

(3)

MSCCH-02 / 900 / 4 (3) (P.T.O.) 209

3) What is neighboring group participation?

n‹S>mogr g‘yh gh^m{JVm {H$go H$hVo h¢? CXmhaU g{hV g‘PmB¶o&

4) Write a note classical carbocation and nonclassical carbocation.

Classical H$m~m}H°$Q>m¶Z d nonclassical H$m~m}H°$Q>m¶Z na {Q>ßnUr {b{I¶o&

5) Discuss free radical addition and Michale addition.

‘w³V ‘ybH$ ¶moJmË‘H$ d ‘mBH$b ¶moJmË‘H$ A{^{H«$¶m H$mo g‘PmB¶o&

6) Discuss conformation of Acylic systems.

AMH«$s¶ V§Ì Ho$ g§ê$nU H$mo g‘PmB¶o&

7) What is cope rearrangement? Give a suitable example.

H$mon nwZ{d©Ý¶mg H$mo CXmhaU g{hV g‘PmB¶o&

OR / AWdm

Explain Fries rearrangement with its mechanism.

’«$mBg nwZ{d©Ý¶mg A{^{H«$¶m H$mo {H«$¶m{d{Y g{hV g‘PmB¶o&

8) Write a short note on Witting reaction.

{dqQ>J A{^{H«$¶m na g§{jßV {Q>ßnUr {b{I¶o&

OR / AWdm

What is Reformatsky Reaction? Explain its mechanism.

[a’$mo‘}Q>ñH$s A{^{H«$¶m {H$go H$hVo h¢? {H$gH$s {H«$¶m{d{Y g‘PmBE&

9) What is the difference between the Inductive and Mesomeric effect? Explain.

àoaU à^md d ‘ogmo‘°[aH$ à^md ‘| A§Va g‘PmBE&

OR / AWdm

What is inductive effect? Discuss its types with examples.

àoaU à^md {H$go H$hVo h¢? BgHo$ àH$ma H$mo CXmhaU g{hV g‘PmB¶o&

(4)

209

MSCCH-02 / 900 / 4 (4)

Section - C 2 × 16 = 32 (Long Answer Questions)

Note: Answer any two questions. You have to delimit your each answer maximum up to 500 words. Each question carries 16 marks.

IÊS> - g (XrK© CÎmar¶ àíZ)

{ZX}e : {H$Ýht Xmo àíZm| Ho$ CÎma Xr{OE& Amn H$mo AnZo CÎma H$mo A{YH$V‘

500 eãXm| ‘| n[agr{‘V H$aZm h¡& à˶oH$ àíZ 16 A§H$m| H$m h¡&

10) Explain EZ system of nomenclature by taking example.

EZ V§Ì Ho$ Zm‘H$aU H$mo CXmhaU g{hV g‘PmB¶o&

11) What are stereoselective reactions? Explain in detail.

{Ì{d‘ daUmË‘H$ A{^{H«$¶m H$mo g‘PmB¶o&

OR / AWdm

What are stereospecific reaction? Explain.

{Ì{d‘ {d{eîQ> A{^{H«$¶m H$mo g‘PmB¶o&

12) Discuss optical activity in spiranes, allene and biphenyls.

ñnmBaoZ, EobrZ d ~mB’o${Zb ‘| àH$m{eH$ g{H«$¶Vm H$mo g‘PmB¶o&

13) Detail the chemistry of electronic spectroscopy give the various types of transition involved in this technique with one example in each case.

Bbo³Q´>mo{ZH$ ñno³Q´>moñH$mo{nH$ Ho$ agm¶Z H$mo g‘PmB¶o& {d{^ÝZ àH$ma Ho$

Bbo³Q´>mo{ZH$ g§H«$‘U H$mo CXmhaU g{hV g‘PmB¶o&

OR / AWdm

How will you synthesize thiophene by the following method.

Wm¶mo’$sZ H$mo {ZåZ{b{IV {d{Y Ho$ Ûmam ~ZmB¶o&

(i) Hiensberg method / {hÝg~J© {d{Y

(ii) From acetylene / EogrQ>rbrZ Ûmam

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