RankLab
Back to Questions
ChemistryHardMCQ2022 · 27 Jun Shift 2

Q46.Decarboxylation of all six possible forms of diaminobenzoic acids C6H3(NH2)2 COOH yields three products A, B and C . Three acids give a product ' A ', two acids gives a product ' B ' and one acid give a product ' C '. The melting point of product ' C ' is (1) 63 °C (2) 90 °C (3) 104 °C (4) 142 °C

What This Question Tests

Requires identifying the possible isomers of diaminobenzoic acids, predicting the products of their decarboxylation (isomers of diaminobenzene), and recalling the melting point of a specific isomer (p-diaminobenzene).

Concepts Tested

IsomerismDecarboxylation reactionMelting points of isomersProperties of diamines

📚 NCERT Sections This Tests

9.9Give The Structures Of A, B And C In The Following Reactions:

Chemistry Class 12 · Chapter 9

76% match

9.9 Give the structures of A, B and C in the following reactions: B NaOH  Br 2 C (i) CH 3 CH 2 I NaCN A Partial OHhydrolysis CuCN H 2 O/H  NH 3 (ii) C 6 H 5 N 2 Cl  A  B  C 4 B HNO 2 C (iii) CH 3 CH 2 Br KCN A LiAlH 0  C  2  2 O/H HCl B H C  (iv) C6 H 5 NO 2 Fe/HCl A NaNO273 K 3 A NaOBr B NaNO 2 /HCl C (v) CH 3 COOH NH 2 B C 6 H 5 OH C (vi) C6 H 5 NO 2 Fe/HCl A HNO273K 279 Amines Reprint 2025-26

9.5How Will You Convert:

Chemistry Class 12 · Chapter 9

76% match

9.5 How will you convert: (i) Ethanoic acid into methanamine (ii) Hexanenitrile into 1-aminopentane (iii) Methanol to ethanoic acid (iv) Ethanamine into methanamine (v) Ethanoic acid into propanoic acid (vi) Methanamine into ethanamine (vii) Nitromethane into dimethylamine (viii) Propanoic acid into ethanoic acid? 9.6 Describe a method for the identification of primary, secondary and tertiary amines. Also write chemical equations of the reactions involved.

9.8Accomplish The Following Conversions:

Chemistry Class 12 · Chapter 9

75% match

9.8 Accomplish the following conversions: (i) Nitrobenzene to benzoic acid (ii) Benzene to m-bromophenol (iii) Benzoic acid to aniline (iv) Aniline to 2,4,6-tribromofluorobenzene (v) Benzyl chloride to 2-phenylethanamine (vi) Chlorobenzene to p-chloroaniline (vii) Aniline to p-bromoaniline (viii) Benzamide to toluene (ix) Aniline to benzyl alcohol.