Amines MCQs

Amines are derivatives of ammonia and are nitrogen-containing organic compounds. When a hydrogen atom in ammonia is replaced by an alkyl or aliphatic group, the result is an alkyl amine. When the hydrogen is replaced by an aryl or aromatic group, it is known as an arylamine. The nitrogen atom in amines contains a lone pair of electrons and is sp3 hybridized, giving the compound a pyramidal shape.

(a) Gabriel phthalimide synthesis
(b) Carbylamine reaction
(c) Stephen’s reaction
(d) Hoffmann bromamide reaction

(d) Hoffmann bromamide reaction

(a) Claisen
(b) Hoffmann
(c) Kekule
(d) Perkin

(b) Hoffmann

(a) On reaction with nitrous acid alkylamines produce alcohol
(b) On reaction with nitrous acid arylamines produce phenol
(c) Alkylamines are more basic than ammonia
(d) Alkylamines are more basic than arylamines

(b) On reaction with nitrous acid arylamines produce phenol

(a) Alkylamines are generally less basic than arylamines because N is sp hybridised
(b) Arylamines are generally more basic than alkylamines due to aryl group
(c) Arylamines are generally less basic than alkylamines due to delocalisation of lone pair of electrons in the benzene ring
(d) Alkylamines are generally less basic than arylamines because lone pair of electrons on N in the arylamines are not delocalised in the benzene ring

(c) Arylamines are generally less basic than alkylamines due to delocalisation of lone pair of electrons in the benzene ring

(a) Ketone
(b) Aromatic acid
(c) Schiff’s base
(d) Carboxylic acid

(c) Schiff’s base

(a) Alkyl nitrite
(b) Secondary amine
(c) Nitroalkane
(d) Alcohol

(d) Alcohol

(a) 4
(b) 2
(c) 5
(d) 3

(a) 4

(a) Azoxybenzene
(b) Aniline
(c) Azobenzene
(d) p-aminophenol

(d) p-aminophenol

(a) Methyl cyanide
(b) Nitroethane
(c) Methyl isocyanide
(d) Acetamide

(c) Methyl isocyanide

(a) Benzylamine
(b) Triphenylamine
(c) p-Nitroaniline
(d) Diphenylamine

(a) Benzylamine