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Organic Chemistry

CSIR NET Chemical Science — Natural Products previous year questions

29 questions · 2011–2019 · all with verified answer · last checked 2026-11-10

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Q1 · June 2019 · 2 marks

Reaction of deoxymonosaccharide A with 2 equivalents of \mathbf{H I O}_{4} affords propanedial, formic acid and formaldehyde. The structure of A is
  • (a) Structure for this question
  • (b) Structure for this question
  • (c) Structure for this question
  • (d) Structure for this question
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Answer: (a)

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Q2 · Dec 2019 · 2 marks

The natural product that gives signal at \delta 218 \mathrm{ppm} in its { }^{13} \mathrm{C} \mathrm{NMR} spectrum
  • (a) \alpha-pinene
  • (b) camphor
  • (c) geraniol
  • (d) carvone
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Answer: (b)

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Q3 · Dec 2018 · 2 marks

The keto-hexose among the following is
  • (a) Xylose
  • (b) Galactose
  • (c) Fructose
  • (d) Mannose
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Answer: (c)

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Q4 · June 2017 · 2 marks

The correct match of natural products in Column-I with their biosynthetic precursors in Column-II is Columnn-I Column-II
  • (a) Structure for this questionI. I-Lysine II. L-Ornithine A-IV, B-I
  • (b) Structure for this questionIII. Farnesyl IV. Geranyl pyrophosphate A-IV, B-II
  • (c) A-III, B-I
  • (d) A-III, B-II
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Answer: (a)

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Q5 · June 2017 · 2 marks

Among the following, the natural product that is a steroid and contains an \alpha,\beta-unsaturated ketone is
  • (a) estrone
  • (b) prostaglandin
  • (c) cortisone
  • (d) morphine
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Answer: (c)

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Q6 · June 2017 · 2 marks

The major product formed in the reaction of D-glucose with 2 ZnCl in MeOH is a methyl glucopyranoside (A or B). The structure of this product and the molecular orbital interaction present between ring-oxygen and the anomeric C-O bond responsible for its stability, respectively, are Structure for this questionStructure for this questionA B
  • (a) A and \mathbf{n} \rightarrow \sigma *
  • (b) A and \mathbf{n} \rightarrow \sigma
  • (c) B and n → σ *
  • (d) B and n \rightarrow \sigma
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Answer: (c)

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Q7 · Dec 2017 · 2 marks

The following natural product Enterodiol is a
  • (a) terpene
  • (b) steroid
  • (c) lignan
  • (d) alkaloid
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Answer: (c)

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Q9 · Dec 2016 · 2 marks

Correct characteristics of the functional groups of adenine in DNA base pair are
  • (a) \mathrm{N}(3) is a hydrogen bond acceptor and \mathrm{C}(6) \mathrm{NH}_{2} is a hydrogen bond donor.
  • (b) \mathrm{N}(1) is a hydrogen bond acceptor and \mathrm{C}(6) \mathrm{NH}_{2} is a hydrogen bond donor
  • (c) Both \mathrm{N}(3) and \mathrm{C}(6) \mathrm{NH}_{2} are hydrogen bond acceptors
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Answer: (b)

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Q10 · Dec 2016 · 2 marks

The correct match for the following is
Column-AColumn-B
(i)Camphor(A)Structural protein
(ii)Insulin(B) Hormone
(iii)keratin(C) Enzyme
(D) Steroid
(E) Terpene
  • (a) (i)-(A); (ii)-(C); (iii)-(E)
  • (b) (i)-(E); (ii)-(B); (iii)-(A)
  • (c) (i)-(D); (ii)-(C); (iii)-(A)
  • (d) (i)-(E); (ii)-(B); (iii)-(D)
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Answer: (b)

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Q11 · June 2015 · 2 marks

Antitubercular drug(s) among the following is (are)
  • (a) Salbutamol A and B
  • (b) Ethambutanol B and C
  • (c) Isoniazid C and D
  • (d) Diazepam D alone
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Answer: (c)

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Q12 · Dec 2015 · 2 marks

The correct match for the compounds in column A with the description in column B is Column A Column B (P) Structure for this question(X) Oil of Wintergreen (Q) Structure for this question(Y) Aspirin (R) Structure for this question(Z) Ibuprofen
  • (a) P-Y, Q-Z, R-X
  • (b) P-Z, Q-X, R-Y
  • (c) P-Z, Q-Y, R-X
  • (d) P-X, Q-Z, R-Y
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Answer: (b)

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Q13 · June 2014 · 2 marks

Atorvastatin (structure given below) is a Structure for this question
  • (a) cholesterol lowering drug
  • (b) blood sugar lowering drug
  • (c) anti-plasmodial drug
  • (d) anti-HIV drug
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Answer: (a)

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Q14 · Dec 2014 · 2 marks

The biosynthetic precursor of abietic acid is
  • (a) Shikimic acid
  • (b) Mevalonic acid
  • (c) Chorismic acid
  • (d) Cinnamic acid
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Answer: (b)

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Q15 · Dec 2014 · 2 marks

The amino acid constituents of artificial sweetener given below are Structure for this question
  • (a) D-Glutamic acid and L-phenylglycine
  • (b) L-Glutamic acid and L-phenylalanine
  • (c) L-Aspartic acid and L-phenylalanine
  • (d) L-Aspartic acid and L-tyrosine
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Answer: (c)

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Q16 · June 2013 · 2 marks

Match the following drugs with their medicinal activity
  • (a) 5-fluorouracil (i) Anti-bacterial A-i, B-ii
  • (b) Amoxicillin lowering (ii) Cholesterol (iii) Anticancer (iv) Anti-inflammatory A-iv, B-iii
  • (c) A-iii, B-iv
  • (d) A-iii, B-i
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Answer: (d)

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Q17 · June 2013 · 2 marks

The biosynthetic precursor for the steroids is
  • (a) secologanin
  • (b) shikimic acid
  • (c) mevalonic acid
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Answer: (c)

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Q18 · June 2013 · 2 marks

Number of isoprene units present in lupeol is Structure for this question
  • (a) two
  • (b) four
  • (c) six
  • (d) eight
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Answer: (c)

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Q19 · June 2013 · 2 marks

\boldsymbol{\alpha}-Pinene on reaction with dilute alkaline \mathbf{K M n O}_{4} produces a diol, which on further oxidation with chromium trioxide gives product A, which undergoes a positive haloform test. The compound A is
  • (a) Structure for this question
  • (b) Structure for this question
  • (c) Structure for this question
  • (d) Structure for this question
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Answer: (c)

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Q20 · June 2013 · 2 marks

The major product formed in the reaction of guanosine with one equivalent of methyl iodide is
  • (a) Structure for this question\mathrm{I}^{\ominus}
  • (b) Structure for this question
  • (c) Structure for this question
  • (d) Structure for this question
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Answer: (a)

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Q21 · June 2013 · 2 marks

Reaction of the dipeptide, given below, with hydrogen in the presence of \mathbf{1 0} \boldsymbol{\%} palladium over carbon, produces a mixture of Structure for this question
  • (a) Gly-Leu + toluene + carbon dioxide
  • (b) Phe-Leu + toluene + carbon dioxide
  • (c) Phe-Leu + benzyl alcohol + carbon dioxide
  • (d) Gly-Leu + benzyl alcohol + carbon dioxide
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Answer: (b)

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Q22 · Dec 2013 · 2 marks

For estrone, among the statements A-C, the correct ones are
  • (a) It is a steroidal hormone A, B and C
  • (b) It has two hydroxyl groups A and B
  • (c) It has one ketone and one hydroxyl groups A and C
  • (d) B and C
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Answer: (c)

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Q23 · Dec 2013 · 2 marks

The peptide A on reaction with 1-fluoro-2, 4-dinitrobenzene followed by exhaustive hydrolysis gave phenylalanine, alanine, serine and N -(2, 4-dinitrophenyl) glycine. On the other hand, pepetide A after two cycles of Edman degradation gave Phe-Ser as the product. The structure of the peptide A is
  • (a) Phe-Ser-Ala-Gly
  • (b) Phe-Ser-Gly-Ala
  • (c) Gly-Ala-Phe-Ser
  • (d) Ala-Gly-Phe-Ser
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Answer: (c)

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Q24 · June 2012 · 2 marks

Among the following, the amino acid which is basic in nature is:
  • (a) Tyrosine
  • (b) Asparagine
  • (c) Leucine
  • (d) Arginine
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Answer: (d)

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Q25 · Dec 2012 · 2 marks

Degradation of penicillin G gives penicillamine that can utilize nitrogen, oxygen or sulfur atoms as donors to bind with lead (II), mercury (II) or copper(II). The structure of penicillamine is
  • (a) Structure for this question
  • (b) Structure for this questionStructure for this question
  • (c) Structure for this question
  • (d) Structure for this question
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Answer: (a)

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Q26 · Dec 2012 · 2 marks

The biosynthetic precursor of cadinene is: Structure for this questionCadinene
  • (a) shikimic acid
  • (b) mevalonic acid
  • (c) arachidonic acid
  • (d) prephenic acid.
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Answer: (b)

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Q27 · Dec 2012 · 2 marks

A tripeptide gives the following products on Edman degradation. Structure for this questionStructure for this questionThe tripeptide is
  • (a) Phe-Ala-Gly
  • (b) Phe-Gly-Ala
  • (c) Ala-Gly-Phe
  • (d) Glv-Ala-Phe
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Answer: (a)

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Q28 · Dec 2012 · 2 marks

Match the following (i) \boldsymbol{\beta}-amyrin
  • (a) alkaloid; secondary alcohol (ii) squalene (i)-(C), (ii)-(D), (iii)-(B), (iv)-(A)
  • (b) alkaloid, phenol (iii) morphine (i)-(B), (ii)-(A), (iii)-(C), (iv)-(D)
  • (c) triterpene, secondary alcohol (iv) ephedrine (i)-(C), (ii)-(B), (iii)-(D), (iv)-(A)
  • (d) acyclic triterpene, polyene (i)-(A), (ii)-(D), (iii)-(B), (iv)-(C)
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Answer: (a)

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Q29 · June 2011 · 2 marks

The major product formed on nitration \left(\mathbf{H N O}_{\mathbf{3}} / \mathbf{H}_{\mathbf{2}} \mathbf{S O}_{\mathbf{4}}\right) of uridine followed by reduction with tin and \mathbf{H C l} is:
  • (a) Structure for this question
  • (b) Structure for this question
  • (c) Structure for this question
  • (d) Structure for this question
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Answer: (c)

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