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Assertion & Reason Test: Amines - NEET MCQ


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12 Questions MCQ Test Chemistry Class 12 - Assertion & Reason Test: Amines

Assertion & Reason Test: Amines for NEET 2024 is part of Chemistry Class 12 preparation. The Assertion & Reason Test: Amines questions and answers have been prepared according to the NEET exam syllabus.The Assertion & Reason Test: Amines MCQs are made for NEET 2024 Exam. Find important definitions, questions, notes, meanings, examples, exercises, MCQs and online tests for Assertion & Reason Test: Amines below.
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Assertion & Reason Test: Amines - Question 1

Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

Assertion (A): Acylation of amines gives a monosubstituted product whereas alkylation of amines gives poly substituted product.

Reason (R): Acyl group sterically hinders the approach of further acyl groups.

Detailed Solution for Assertion & Reason Test: Amines - Question 1
In alkylation, an amine can react with alkyl halide to form next higher class of amine caused by the presence of electron pair on nitrogen which makes amine to behave as nucleophile and alkyl halide thus undergo nucleophilic substitution reaction. When primary and secondary amines react with acid chlorides, anhydrides and esters to give monosubstituted amides as products. Acylation is carried out in the presence of a base stronger than the amine like pyridine which causes the shift of the equilibrium to the right side.
Assertion & Reason Test: Amines - Question 2

Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

Assertion (A): Aromatic 1° amines can be prepared by Gabriel Phthalimide synthesis.

Reason (R): Aryl halides do not undergo nucleophilic substitution with anion formed by phthalimide.

Detailed Solution for Assertion & Reason Test: Amines - Question 2
Aromatic 1° amines cannot be prepared by Gabriel Phthalimide synthesis because aryl halides do not undergo nucleophilic substitution with anion formed by phthalimide.
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Assertion & Reason Test: Amines - Question 3

Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

Assertion (A): Acetanilide is less basic than aniline.

Reason (R): Acetylation of aniline results in decrease of electron density on nitrogen.

Detailed Solution for Assertion & Reason Test: Amines - Question 3
Acetanilide is less basic than aniline as in amides the carbonyl group (C=O) is a stronger dipole than N-C dipole. Therefore, the ability of N-C group to act as H-bond acceptor (as a base) is restricted in the presence of a C=O dipole.
Assertion & Reason Test: Amines - Question 4

Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

Assertion (A): N, N-Diethylbenzene sulphonamide is insoluble in alkali.

Reason (R): Sulphonyl group attached to nitrogen atom is strong electron withdrawing group.

Detailed Solution for Assertion & Reason Test: Amines - Question 4
N, N-Diethylbenzene sulphonamide is insoluble in alkali because it has no acidic hydrogen. Sulphonyl group attached to nitrogen atom is electron withdrawing group.
Assertion & Reason Test: Amines - Question 5

Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

Assertion : Nitrating mixture used for carrying out nitration of benzene consists of conc. HNO3+ conc. H2SO4

Reason : In presence of H2SO4, HNO3 acts as a base and produces NO2+ ions.

Assertion & Reason Test: Amines - Question 6

Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

Assertion : Acylation of amines gives a monosubstituted product whereas alkylation of amines gives poly-substituted product.

Reason : Acyl group sterically hinders the approach of further acyl groups

Detailed Solution for Assertion & Reason Test: Amines - Question 6
Acylation of amine gives a mososubration product whereas alkyation of amine gives polysubstituted product because acylation in amine takes place at N-atom and alkylation takes place at o and p position.
Assertion & Reason Test: Amines - Question 7

Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

Assertion : Aniline does not undergo Friedel-Crafts reaction.

Reason : –NH2 group of aniline reacts with AlCl3 (Lewis acid) to give acid-base reaction.

Detailed Solution for Assertion & Reason Test: Amines - Question 7
Aniline does not undergo Friedel craft's reactions because the reagent AlCl3 ​ (the Lewis acid which is used as a catalyst in friedel crafts reaction), being electron deficient acts as a Lewis base. and attacks on the lone pair of nitrogen present in aniline to form an insoluble complex which precipitates out and the reaction does not proceed.
Assertion & Reason Test: Amines - Question 8

Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

Assertion : Nitration of aniline can be conveniently done by protecting the amino group by acetylation.

Reason : Acetylation increases the electron-density in the benzene ring.

Detailed Solution for Assertion & Reason Test: Amines - Question 8
Acetylation decreases the electron-density in the benzene ring thereby preventing oxidation.
Assertion & Reason Test: Amines - Question 9

Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

Assertion : Acetanilide is less basic than aniline.

Reason : Acetylation of aniline results in decrease of electron density on nitrogen.

Detailed Solution for Assertion & Reason Test: Amines - Question 9

Assertion & Reason Test: Amines - Question 10

Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

Assertion : Amines are basic in nature.

Reason : Amines have lone pair of electrons on nitrogen atom.

Detailed Solution for Assertion & Reason Test: Amines - Question 10
Amines are basic due to the presence of a lone pair of electrons on nitrogen atom. The lone pair can be easily donated.
Assertion & Reason Test: Amines - Question 11

Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

Assertion : Only a small amount of HCl is required in the reduction of nitro compounds with iron scrap and HCl in the presence of steam.

Reason : FeCl2 formed gets hydrolysed to release HCl during the reaction.

Detailed Solution for Assertion & Reason Test: Amines - Question 11

Fe + 2HCl → FeCl2 + 2[H]

Nacent hydrogen is reduced into nitro compounds.

FeCl2 + H2O(g) → FeO + 2HCl

Hence, (iv) Both assertion and reason are correct statements and reason is the correct explanation of assertion.

Assertion & Reason Test: Amines - Question 12

Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

Assertion : Aromatic 1°amines can be prepared by Gabriel phthalimide synthesis.

Reason : Aryl halides undergo nucleophilic substitution with anion formed by phthalimide.

Detailed Solution for Assertion & Reason Test: Amines - Question 12
Aromatic primary amines cannot be prepared by Gabriel phthalimide synthesis because it used for the preparation of aliphatic primary amines. It involves nucleophilic substitution (SN2) of alkyl halides by the anion formed by the phthalimide. But aryl halides do not undergo nucleophilic substitution with the anion formed by the phthalimide.

Hence, aromatic primary amines cannot be prepared by Gabriel pthalimide synthesis.

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