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MSCCH-02

June - Examination 2019

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¡&

209

MSCCH-02 / 1000 / 4 (1) (P.T.O.)

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209

MSCCH-02 / 1000 / 4 (2) (Contd.)

1) (i) Write the difference between configuration and conformation?

g‘Zwê$n VWm A{^{dݶmg ‘| {d^oXZ H$s{OE&

(ii) Illustrate the following with suitable examples:

{ZåZ H$mo Cn¶w³V CXmhaUm| Ûmam àX{e©V H$s{OE&

(a) Fisher projection formula

{’$ea àjonU gyÌ

(b) Newman's projection formula

ݶy‘m°Z àjonU gyÌ

(iii) What is chemical shift?

amgm¶{ZH$ {dñWmnZ ³¶m h¡?

(iv) Write the lab method for the preparation of pyrolle.

nmBamob Ho$ {Z‘m©U H$s à¶moJembm {d{Y {b{IE&

(v) Explain orientation and chemical properties of Furan.

â¶yaoZ Ho$ A{^{dݶmg Ed§ amgm¶{ZH$ JwU {b{IE&

(vi) What is Nitrene? Write its properties.

ZmBQ´>rZ ³¶m h¡? CgHo$ JwU {b{IE&

(vii) Explain the properties of Enantiomers.

BZoZ{g¶mo‘a Ho$ JwU g‘PmBE&

(viii) Explain in short catalytic Hydrogenation.

CËào[aV hmBS´>mo{OZrH$aU H$mo g§{jßV ‘| g‘PmBE&

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MSCCH-02 / 1000 / 4 (3) (P.T.O.) 209

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) Explain the Kekule structure of Benzene and its molecular formula.

~oÝOrZ H$mo Ho$Hy$bo g§aMZm VWm CgH$m AmpÊdH$ gyÌ g‘PmBE&

3) Discuss optical activity in molecules having no chiral carbon.

CZ AUwAm| H$s àH$mer¶ J{V{d{Y H$mo g‘PmBE {OZ‘| H$moB© {H$ab H$m~©Z Zht hmoVm&

4) What is NMR spectroscopy? Why is TMS a good standard?

NMR ñno³Q´>moñH$monr ³¶m h¡? TMS EH$ AÀN>m ‘mnX§S> ³¶m| h¡?

5) Write the chemical reactions and physical properties of Pyridine.

{n[a{S>Z H$m amgm¶{ZH$ VWm ^m¡{VH$ JwU {b{IE&

6) Explain the structure and Aromaticity in Thiophene.

WmB¶mo’$sZ H$s g§aMZm VWm Eoamo‘o{Q>{gQ>r H$mo g‘PmBE&

7) What are Heterocyclic compounds ? Explain their nomenclature and classification.

{df‘ MH«$s¶ ¶m¡{JH$ ³¶m h¡? CZH$m Zm‘H$aU VWm dJuH$aU {b{IE&

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209

MSCCH-02 / 1000 / 4 (4)

8) Write the preparations and chemical properties of carbonations.

H$m~m}Ho$Q>mBZ H$s {Z‘m©U {d{Y VWm amgm¶{ZH$ JwU {b{IE&

9) Explain structural orientation and regioselectivity.

g§aMZmË‘H$ A{^{dݶmg VWm [a{O¶moñbop³Q>{dQ>r

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 AnZo CÎma H$mo A{YH$V‘ 500 eãXm| ‘| n[agr{‘V H$s{OE& à˶oH$ àíZ 16 A§H$m| H$m h¡&

10) Explain conformational analysis of acyclic molecules.

A{^{dݶmg {díbofU (AMH«$s¶ AUwAm| Ho$) H$mo g‘PmBE&

11) Describe SN1 mechanism with examples. Explain neighbouring group participation.

SN1 {H«$¶m{d{Y H$mo g‘PmBE& nS>mogr g‘yh ¶moJXmZ H$mo g‘PmBE&

12) Give a detailed comparison between E1, E2 and Ecb reactions.

E1, E2VWm Ecb A{^{H«$¶mAm| H$m {dñV¥V VwbZmË‘H$ dU©Z H$s{OE&

13) Describe the oxidation of aromatic rings and alcohols

Eamo‘o{Q>H$ [a¨J VWm EëH$mohm°b Ho$ Am³grH$aU H$mo g‘PmBE&

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