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Oc Dpp-16ealdehydeandketone
Oc Dpp-16ealdehydeandketone
1.
(a) (b)
(c) (d)
2. ; product X is :
3. ; product is :
4. ; product is :
5. ; product is :
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6. ; product is :
8.
W is sweet smelling compound and liberates H2 with Na metal. Identify the correct option.
(a) (b)
(c) (d)
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12. What will be the product of the following reaction Ph(Me)CHCOMe ?
RCO H
Ph(Me)CHCOMe
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(a) (b)
O
O
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18. PhCHO + (CH3CO)2O A B. The product B is :
CH3COONa HBr
(a) PhCH = CHCH2Br (b) PhCH CH 2 COOH (c) PhCH2CH(Br)COOH (d) PhCH = CH–COBr
|
Br
19. Among the following which one will show significant hydration ?
(a) I and III (b) II and III (c) III and IV (d) I and II
20. The number of stereoisomeric products formed in the following reaction is
Cl
22. The structure of major product (pseudoionone) is,
CHO
HCHO (excess)
23. The end products of following reaction would be, NaOH (excess)
C
O CH3
C C C C
O CH3 O C(CH3OH) 3 O C(CH3OH) 3 O C(CH3OH) 3
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25. In which of the following compounds O18 exchange can be observed on keeping it in H2O18
27. The possible number of stereoisomers of the product of following reaction would be:
NH2OH
CH3–CH = CH – CH – CHO
CH3
(a) 2 (b) 4 (c) 6 (d) 8
28. Which of the following ketone racemises in aqueous solution containing some acidic or basic impurities.
NH 2OH.HCl
(1)
(A)
PCl5
(2)
(B)
Br2 / Fe
(3)
(C)
(a) (b)
(c) (d)
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Pd – CaCO , H
CH3COCH 3 A B C
H C C C Na + H O Al O
32. 3 2 3 2 2 3
D
CH3
|
(a) CH2=CH—CH=CH2 (b) CH=CH—CH=CH2 (c) CH==C—C==CH2 (d) None of these
| |
CH3 CH3
33. Given the set of reactions. Identify the end product
35.
H+
36.
H2O
N
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O
O C OC2H5 +
(1)HCl (i)LiAlH4/Et2O
37. X Y Z; Identify X, Y and Z
H3 O
CH2OH
38. Arrange the following compounds in decreasing orders of Keq for hydrate formation.
(a) Z > Y > X > W (b) Z > X > Y > W (c) Z > W > X > Y (d) Z > X > W > Y
39. Give the correct sequence of reagents for the following conversion :
(a)
(b)
(c)
(d)
C O
40. What product is formed in the following reaction HO Ag2O
H
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41. Which ketone is most reactive in carbonyl addition reaction
O O
(a) (b)
(c) (d)
43. Given a set of reactions. Identify the compound W
1-heptyne S T U V W
LiNH 2 1–Chloro–3–bromopropane (1) Mg H2, Lindlar’s catalyst CrO3
(2) n–C10 H21CHO / H
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46. The product of the following reaction are (Hint: Cannizzaro type reaction),
PhMgBr + 2PhCHO
(a) (b)
(c) (d)
O
S S
(a) S S
(b) S S
(c) (d) C
Li R' R''
H R' R' R'' H
48. Glyceraldehyde is commonly made from the oxidaton of
(a) Acrolin (b) Acetal of acrolin (c) Glycerol (d) Hemiacetal of acrolin
Multiple Choice Questions
Ph CH
1.PCl5 / Ether H2 O
49. C N A B+C A, B, C are
pCH3C6H4 2.H2O
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53. Which of these carbonyl compounds oh reduction with Zn - Hg / HCI will give the same compound as
product
(a) (b)
(c) (d)
54. Given the statements for a compound C10H16O which on vigrous oxidation yields acetone, oxalic acid
and CH3COCH2CH2COOH, are true
(a) It reacts with hydroxylamine to give C10H17ON
(b) It reduces with Tollen’s reagent to give a compound C10H16O2
(c) It has 2 stereoisomers (d) It is optically active
55. NH2NHCONH2 (1 mole) when added to a mixture of cyclohexanone (1 mole) and benzaldehyde (1
mole) then the product are
(a) Semicarbazone of cyclohexane (kinetically controlled)
(b) Semicarbazone of benzaldehyde (Thermodynamically controlled)
(c) Semicarbazone of benzaldehyde (kinetically controlled)
(d) Semicarbazone of cyclohexane (Thermodynamically controlled)
56. Anhydrous acids bring about formation of acetals where as aqueous acids bring about hydrolysis of
acetals because
(a) High alcohol, low water concentration shift the hemiacetal-acetal and aldehyde-hemiacetal equilibria
in the direction of the acetal.
(b) Low alcohol, high water concentrations shift the equilibria in the direction of aldehyde.
(c) Reverse statements of A and B are true (d) None of these
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60. The suitable reagents of the following reaction are :
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All students are advised to solve DPPs within allowed time only.
All discussions are scheduled in every 4th doubt discussion class
–MKA Sir (Guruji)
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