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Chemistry Exam: Organic Chemistry II, 2nd Semester, 2063, Study notes of Pharmaceutical Chemistry

A past exam paper for the organic chemistry ii course during the 2nd semester of the academic year 2063. The exam consists of three sections: a, b, and c. Section a contains compulsory questions worth 30 marks, while sections b and c have five questions each worth 5 marks. Topics covered in the exam include aufbau principle, conformational isomerism, carbocations, structural isomerism, acids and bases, aromatic compounds, and reactions. Students are required to define, discuss, write notes, and draw structures for various compounds and concepts.

Typology: Study notes

2010/2011

Uploaded on 10/03/2011

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11 I iJi' ilT
iTciai
l'jo.
of Prinied
Fagevri.'
1.2.4
Pharmaceutica
I
Chemistry-Ill
-(Organic
Chernistry-I)
(8.
Pharm
acy,2nd Semester,
2063)
Time:3
Hours] [Ma,rimum
Marks:
80
llote:-section
A is compulsory.
Attempt
Four
questions
from Section B and any Three
questions
from Section C.
Section-A Marks:30
Define
Aufbau
PrinciPle.
PCl. dissociates
to
give
PCl..
Why ?
Discuss
conformational
isomerism.
Write
note
on
carbenes.
Whai ejo you mean by F ans S
configurations
?
v i,.,,i: r\:rne ihe crorbitals
involved
in :
\vr,/ rrerrrv
'..) S,r"t i iyi;riuiisaiic;ri, ancJ
i
), Stl,12
hvirririi54iinn
;,r
:i Er:,'ieili i'l"igrkc'v,ri:ikcv's
r't.lie.,
.1
j ,2
d Turn Over
tt A
U--?
1. (i)
(ii)
(
iii)
(iv)
ii/ |
pf3
pf4

Partial preview of the text

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1 1 I i J i ' i l T

iTciail'jo.of PriniedFagevri.'

1.2.

Pharmaceutica I Chemistry-Ill

  • (Organic Chernistry-I)

(8. Pharmacy,2ndSemester,

T i m e : 3H o u r s ]

[Ma,rimum

Marks:

llote:-section A is compulsory. AttemptFour

questionsfrom SectionB and any Three

questionsfromSectionC.

Section-A Marks:

DefineAufbau

PrinciPle.

PCl.dissociatesto givePCl..Why

Discuss conformationalisomerism.

Writenoteoncarbenes.

W h a i e j o y o u m e a n b y

F

a n s

S

configurations

v

i,.,,i: r:rne ihe crorbitals involvedin : \ v r , /

r r e r r r v

'..) S,r"t i iyi;riuiisaiic;ri,ancJ

i ) , S t l , 1 2 h v i r r i r i i 5 4 i i n n

;,r:i Er:,'ieili i'l"igrkc'v,ri:ikcv's r't.lie.,

. 1

j ,

d TurnOver

t t A

U--?

( i )

( i i )

(iii)

(iv)

i i / |

( 2 )

/,t

f ( d ) G i v et h e r e q u i r e m e n t s

o f a c o m p o u n d

.shoryin

g opticalactivity.

-(!]r;Flt

whytrimerhyiamine

is lessbasic

gaffdl-methytamine.

iiie ciown the structui.aifcrmuia of all the

F n m ^ ^. - r

  • v r r r y w u r r U S W n l C n D O s s p c e f n r m , , , ^

/ 1 l t

' v l l l l l i l A

u < n r r ( J.

Write thesiructur.al foi-muia fo;.each of ihe

following compounds :

3 - E i n y i - 2 - m e t h y l - p e n t a n e

( i i ) 1 , 3 - B u t a d i e n e

Define andclassify structural lsomerism.

Explainbrieflywhy chlorohcetic

acid is a

stronger acidthanacetic acid.

F o r. t h e f o l l o w i n g p o i n to u t t h e c o r r e c t

o r i e n t i n g ' n a t u r e o f e a c h g r o u p w h e n

present in an aromatic nucleus :

Idl

(i)

(ii)

(i'i)

(iv)

  • B r
  • cooH

-oH

  • crH,

i i

_g.lacg,

aceirc , ^

acrd-66il--

v

/r-\ I

(v) lso-propyl alcohol

t"')

A

;?^:

B

N a L 0 3

Explairtthe followitrg

(a) SandgneyerReaction

(b) WilliamronSynthesis

(c) Fittig'sReaction

(d) Benzoin condensation

(e) Metamerism.

How wiil you convert:

(a) Acetaldehyde to Lacticacid

(b) Toiueneto benzene

(c) Acetyleneto Aceticacid

(d) Oxaiicacidto Cyanogen

i o \ E l h r r i a l n n h n t

  • 1 l \ / n! 1 1 1 1

\ v , ,

L r r t t r g r v v l r v l t v r Y r v r r. q r i v '

(a) ExplainResonance.

Boil

. .\

K l l H

' ^ -

l " l v

v

2x

-tE

it') Write

structuralformuiae

ancj

iijPACnames

of variousstructurai

isomershavinqthe

m O i e C U l a ; ' i C i ' n ' r r i : e

H

3 r

, u , u v : , , l _.

ic)

l-iow wortid you r-:frnrifii napirlaien? inio

2-nitrcnaphthalene

r i J
i i / h?. r d , :

\ / /
_ ,

|

^ n n f i n 1 , r : i i : t n. q

" r

,

i

I < n r

| |. 2. +

u-