Organic DPT 1-14
Organic DPT 1-14
Organic DPT 1-14
COOH
2. CH2–C–—CH2
OH OH OH
3. CH3
HO
CH3
CO2H
4.
Cl Br
H 3C OH
5.
H3C CH3
CH=CH–CHCH2CH3
6. CH3
7.
8.
9.
10.
O
CH2 CH2CH2CH3
11.
O O
C–NH2
NC Ph
O
H2 N OH
H O
Based on given molecule
CH3 CH3
6. and
CH3
Number of secondary carbon atoms present in the above compounds are respectively :
N N
(A) (B) N N
N N
(C) (D)
OH OH
OH
(A) (B) (C) (D) None
OH OH OH
OH OH
This section contains 10 multiple choice questions. Each question has four choices (A), (B), (C) and
(D) out of which ONE or MORE are correct. 4(–2)
1. Which of the following compound contain all 1º, 2º & 3º amine
N NH2
N N
(A) (B)
N N
N NH2
(C) (D) H2N NH NH2
N
H
OH O Cl
O–H
2.
O
NH2 CH3
(A) (B) CH3–C–NH2 (C) CH3–NH2 (D) None
CH3
H3C O CH3
4. Present functional group is
H3C O CH3
O
H2N
OH
HO
O
H O NH2
NH2 H
N
(C) (D)
O H H
N N
(i) O (ii) H O
N O
Me
OH
O
O
O Cl
(iii) (iv) H
H
O O O O
OH O
O
O
O OH O
O
N
(v) (vi)
O
NH2
O O O O NH2
H
COOH O Me
O
H OH OH O
(vii) (viii) (ix) (x) O O
H OH
COOH O
COOH Me
COOH H
O O O O O
(A) —C—O—C— (B) —C—H (C) —C— (D) —C—OH
4. Which is not a hydrocarbon.
OH
(CH3CO)2N-ph
'A' 'B'
15.
Br
O
(A) 5-bromo-2-chloro-1,4-epoxy cyclohexane (B) 2-bromo-5-chloro-1,4-epoxy cyclopentane
O
(A) 5-ethyl-2-methyl cyclohexa-2,5-diene-1,4-dione (B) 2-ethyl-5-methyl cyclohexa-2,5-diene-1,4-dione
O OH O
O
O
O O
(A) 2-Methanoyloxy-2-ethoxy carbonyl-3-oxo-butanoic acid
(B) 4-Bromo-1-carboxy-3-chloro-beneze
COOH
(A) (B) (C) (D)
N
9. The structure of spiro [3,3] heptane is:
(A) Tartic acid (B) Lactic acid (C) Malic acid (D) Citric acid
COOH
OH
CHO
This section contains 3 questions. The answer to each question is a single digit Integer, ranging from
2. Number of possible organic compound with different structure & IUPAC name p1-bromo-p2-chloro
cyclohex-p3-enone for minimum value of p1 + p2 + p3 . Where pi indicates position of side chains &
functional groups.
Br
x
3. Find the value of (x + y) in a compound Cl where x & y represents position of
y
O
(A) Carboxylic acid -C-OH (B) Aldehyde –C
O H
O
(C) Ester C O (D) Anhydride –C–O–C
G O O
2. A compound C contain / ratio, 1 : 1 if G is -
G G
G
CHO OH O
NC NH
NH
NC
O CH2OH
CH2-CH3
CH3-CH-CH-CH3
CH2-CH3
11. Which of the following is not correct about member of any homologous series :
(A) They have similar chemical properties (B) They have similar physical properties
(C) They differ by a –C2H5 or its multiple (D) They can not be represent by same general formula
This section contains 1 questions. The answer to each question is a single digit Integer, ranging from
1. Minimum value of (p1 + p2 + p3 + p4) where pi represents position of substituents & functional group
CN
O CH2–OH
CHO
O
(A) 9 (B) 10 (C) 11 (D) 12
3. Which of the following is/are homocyclic compound ?
N O N
(I) | (III) (IV) (V) | (VII) (VIII)
H H
(II) (VI)
(A) I, IV, VI (B) II, III, IV (C) I, VII, VIII (D) IV, V
(C) There are only three compounds which contains only 2º carbon
(D) Among all compounds there are four different functional groups are present
HO
O
(A) 3,5-diethyl-2-methyl-4-propyloct-5-enoic acid
(B) 4,6-diethyl-7-methyl-5-propyloct-3-enoic acid
(C) 2-methyl-3,5-diethyl-4-propyloct-5-enoic acid
(D) 3,5-diethyl-2-methyl-4-propyloct-6-enoic acid
6. Which of the following is not a homocyclic compound
(A) Phenol (B) Aniline (C) Ethylene epoxide (D) Benzene
7. Which of the following compound have even number of degree of unsaturation ?
CN
O H3C–C=O
NH
OH
(A) (B) (C) (D) H3C–C C—Ph
OH N
O COOH
O CH = O
O O
CH3O–C O–C–CH3
COOH
This section contains 2 questions. The answer to each question is a single digit Integer, ranging from
1. Number of carbon atoms in the principal carbon chain of the given compound is :
CH = O
CH3 – CH – CH — CH
OH CH
CH2
2. An open chain unbranched alkane, isolated from species of blue-green algae has a molecular weight
(C) sp2 and sp carbon atoms (D) sp3, sp2 and sp carbon atoms
O
(B) (q) Heterocyclic compound
(A) (B)
7. Calculate molecular weight of the lowest alkane containing a sequence of 10, 20, 30 and 40 carbon atoms.
CH2 — CH3
|
(A) CH3 — CH — CH2 — CH — CH3 (B)
|
CH2 — CH3
CH3
|
(C) (D) CH3 — CH — CH2 — CH2 — CH — CH2 — CH3
|
CH2 — CH3
3. In following compound -
CH3 CH3
CH3 CH3
The correct lowest set of locants are
(A) 3,3,4,5 (B) 3,4,5,5 (C) 4,5,3,3 (D) 5,5,4,3
7. Calculate the molecular weight of the lowest hydrcarbon which contains sp & sp2 hybridised carbon atoms
only.
Br Br
1. The correct IUPAC name of H3C – C – CH – C – CH3
F C2H5 I
(A) 2,4-Dibromo-3-ethyl-2-fluoro-4-iodopentane (B) 2,4-Dibromo-3-ethyl-4-fluoro-2-iodopentane
(C) 2,4-Dibromo-4-fluoro-2-iodo-3-ethylpentane (D) 2,4-Dibromo-2-fluro-4-iodo-3-ethylpentane
2. The correct IUPAC name of the following compound is :
(A) (B)
(C) (D)
(A) 2,3–Diethylbutene
8. Comprehension #
While naming unsaturated hydrocarbons, lowest locant is alloted for multiple bond than any substituent,
since the priorty of multiple bond is more than any substituent present. When the locant for unsaturated is
same from either side then double bond is given priority over triple bond. For main chain selection if the
size of main chain and number of unsaturation are equal, then priority is given to the lowest set of locants
for unsaturation.
(a) IUPAC name of the following compound is
(A) 3-(Prop-2-ynl)hexe-1,3,5-triene
(B) 4-Ethenylhepta-1, 3-dien-6-yne
(C) 4-Ethenylhexa-4, 6-dien-1-yne
(D) 4-(Prop-2-ynyl) hexa-1,3,5-triene
(A) 4–Fluoro–1–methoxypent–1–yn–4–ene
(B) 1–Fluoro–1–methyl–4–methoxybut–1–en–3–yne
(C) 4–Fluoro–1–methoxypent–3–en–1–yne
(D) 2–Fluro–5–methoxypent–2–en–4–yne
(c) IUPAC name of the following compound is
1. IUPAC name of is
O
3. Correct IUPAC name of the compound is
Me
O
Statement-2 : In case of chain terminating senior most functional group numbering starts from itself.
(A) Statement-1 is True, Statement-2 is True; Statement-2 is a correct explanation for Statement-1.
(B) Statement-1 is True, Statement-2 is True; Statement-2 is NOT a correct explanation for Statement-1.
(C) Statement-1 is True, Statement-2 is False.
(D) Statement-1 is False, Statement-2 is True.
(C) 5-Ethyl-1-methylcyclohex-1-ene
(D) 4-Methyl-3-oxopentan-2-ol
6. Comprehension #
Bicyclo compounds are named by using the alkane name to designate the total number of carbon and
bicyclo is used as prefix. While naming the bicycloalkane we write an expression between the word
bicyclo and alkane (in square bracket), that denotes the number of carbon atoms in each bridge. The
numerals are written in descending order and the numbers are separated by full stops.
COOH
(P) (W) 3-[2-(2-Oxoethyl)phenyl]propanoic
acid
CHO
CHO
CH2CH2COOH
(R) (Y) 2-(2-Formylphenyl)ethanoic acid
CH2 CHO
CH2 – COOH
(Z) 2-Formylbenzenecarboxylic acid
(S)
CH2CH2CHO
ANSWER KEY
DPT # 01
S.NO. 1ºC 2ºC 3ºC 4ºC 1ºH 2ºH 3ºH IHD
1 4 5 2 0 12 10 2 0
2 3 0 1 0 4 0 0 1
3 4 4 0 2 12 7 0 1
4 3 3 1 0 6 4 1 1
5 3 1 3 0 9 1 1 2
6 2 8 2 0 6 10 2 4
7 3 6 1 0 6 9 1 3
8 3 4 1 0 5 2 1 5
9 5 1 3 0 15 2 1 1
10 2 2 2 0 6 2 0 3
11 1 8 1 0 3 13 0 3
DPT # 02
SECTION–I : 4(–2)
1. (A,C,D) 2. (A,B,C) 3. (C) 4. (D) 5. (C,D)
6. (A) 7. (C) 8. (A,B,C,D) 9. (A,B,C) 10. (B,C)
DPT # 03
SECTION–I : 4(–2)
1. (B,C) 2. (D) 3. (A,B,C) 4. (C) 5. (B,C,D)
6. (A,C,D) 7. (A,B,C) 8. (D) 9. (D) 10. (B,D)
DPT # 04
SECTION–I : 4(–2)
1.(5) 2. (5) 3. (8) 4. (4) 5. (5) 6.(11) 7.(2) 8.(3)
9. (4) 10. (5)
DPT # 05
SECTION–I : 4(–2)
1. (A) 2. (C) 3. (A,B,C,D) 4. (A,D) 5. (B)
6. (B) 7. (D) 8. (A) 9. (A,B,C) 10. (A)
11. (C) 12. (D) 13. (B,C,D) 14. (C) 15. (D)
SECTION-IV : 4(–2)
1. (2) 2. (2) 3. (5)
DPT # 07
SECTION–I : 4(–2)
1. (A,B,C) 2. (B) 3. (D) 4. (D) 5. (A)
6. (A,B,D) 7. (B) 8. (A,B,C) 9. (A) 10. (A,B,C,D)
11. (B,C,D)
SECTION-IV : 4(–2)
1. (6)
DPT # 08
SECTION–I : 4(–2)
1. (B) 2. (C) 3. (A,B,D) 4. (C) 5. (A,B,D)
6. (A) 7. (C,D) 8. (A,B,C,D) 9. (A)
SECTION-IV : 4(–2)
1. (4) 2. (5)
DPT # 09
SECTION–I : 4(–2)
1. (A,C,D) 2. (A, B, C, D) 3. (A,B,C,D) 4. (A,B,C) 5. (A)
6. (C) 7. (B,D) 8. (C) 9. (A) 10. (B)
SECTION-IV : 4(–2)
1. (5) 2. (2)
DPT # 11
1. (B) 2. (C) 3. (D) 4. (D) 5. (B)
6. (A,B) 7. 114. 8. A S, B P, C Q, D R
DPT # 12
1. (C) 2. (C) 3. (A) 4. (D)
5.* (A,B,D) 6.* (A,B,C,D)
7. H2C = C = CH2
M. W. = 40. 8. [A – s] ; [B – q] ; [C – p] ; [D – r]
DPT # 13
1. (A) 2. (D) 3. (C) 4. (B)
5. (B,C,D) 6. (B,C,D) 7. 6
8. (a) (B) (b) (C) (c) (D)
DPT # 14
1. (C) 2. (A) 3. (A) 4. (A) 5.* (A, D)
6. (a) (C) (b) (C) 8. (P Z) ; (Q Y) ; (R W) ; (S X).