Some statements are given about acylation of amines with acid chloride

I. Tertiary amines do not react with acid chloride

II. This reaction is an example of a nuclophilic addition reaction

III. This reaction is carried out in the presence of pyridine

IV. Aliphatic and aromatic primary and secondary amines involve in this reaction

The correct statements is/ are

I, II, III only

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I, III, IV only

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II only

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IV only

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Solution

The correct option is B I, III, IV only
Statement II refers to is a nucleophilic substitution reaction

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Similar questions

Some statements are given about acylation of amines with acid chloride

I. Tertiary amines do not react with acid chloride

II. This reaction is an example of a nuclophilic addition reaction

III. This reaction is carried out in the presence of pyridine

IV. Aliphatic and aromatic primary and secondary amines involve in this reaction

The correct statements is/ are

Q. Write the reactions of (i) aliphatic and (ii) aromatic primary amines with nitrous acid:

Q. Primary amine with ketone under acidic condtion:

Regarding this reaction correct statement(s) is/are:

Q. The carboxylic acids react with hydrazoic acid in presence of

H_{2} S O_{4}

to form a primary amine. This reaction is called as :

Account for the following:

(i) pK_bof aniline is more than that of methylamine.

(ii) Ethylamine is soluble in water whereas aniline is not.

(iii) Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.

(iv) Although amino group is o, p− directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.

(v) Aniline does not undergo Friedel-Crafts reaction.

(vi) Diazonium salts of aromatic amines are more stable than those of aliphatic amines.

(vii) Gabriel phthalimide synthesis is preferred for synthesising primary amines.

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The correct option is B I, III, IV onlyStatement II refers to is a nucleophilic substitution reaction

The correct option is B I, III, IV only
Statement II refers to is a nucleophilic substitution reaction