Advertisements
Advertisements
प्रश्न
Which of the following methods of preparation of amines will give same number of carbon atoms in the chain of amines as in the reactant?
पर्याय
Reaction of nitrite with \[\ce{LiAlH4}\].
Reaction of amide with \[\ce{LiAlH4}\] followed by treatment with water
Heating alkyl halide with potassium salt of phthalimide followed by hydrolysis.
Treatment of amide with bromine in aqueous solution of sodium hydroxide.
Advertisements
उत्तर
Heating alkyl halide with potassium salt of phthalimide followed by hydrolysis.
Explanation:
Aliphatic and arylalkyl primary amines can be prepared by the reduction of the corresponding nitriles with \[\ce{LiAlH4}\].
\[\ce{\underset{Alkynitrite}{R - C ≡ N} \underset{Arynitrite}{Ar - C ≡ N} -> LiAlH4 RCH2\underset{1° amine}{NH2} or ArCh2NH2}\]
Heating alkyl halide with primary, secondary and tertiary amine can be prepared by reduction of \[\ce{LiAlH4}\] followed by treatment with water.
\[\ce{\underset{1° amide}{R - CONH2} ->[(i) LiAlH4][(ii) H2O] R - CH2 - NH2}\]
Heating alkyl halide with potassium salt of phthalimide followed by hydrolysis produces primary amine. This process is known as Gabriel phthalimide reaction. The number of carbon atoms in the chain of amines of product is same as reactant.

APPEARS IN
संबंधित प्रश्न
Write a short note on Hoffmann bromamide degradation.
An aromatic compound 'A' of molecular formula C7H7ON undergoes a series of reactions as shown below. Write the structures of A, B, C, D and E in the following reactions :

Give the structures of A, B and C in the following reactions :

Name the process of breaking C-X bond by ammonia in preparation of amines.
Acetamide on reduction using Na/C2H5OH gives ____________.
Alkyl cyanides on reduction by sodium and ethanol give primary amines. This reaction is called as ____________.
Identify the product obtained, when benzamide is treated with bromine and aqueous sodium hydroxide.
Which of the following compounds is obtained when quaternary ammonium hydroxide is strongly heated?
Which of the following reactions does NOT yield an amine?
Which of the following amines can be prepared by Gabriel synthesis.
(i) Isobutyl amine
(ii) 2-Phenylethylamine
(iii) N-methylbenzylamine
(iv) Aniline
How will you carry out the following conversion?

How will you carry out the following conversions?

Assertion: Aromatic 1° amines can be prepared by Gabriel Phthalimide Synthesis.
Reason: Aryl halides undergo nucleophilic substitution with anion formed by phthalimide.
A primary amine is formed by an amide on treatment with bromine and alkali. The primary amine has
Which of the following amines can be prepared by Gabriel phthalimide reaction?
The amine 'A' when treated with nitrous acid gives yellow oily substance. The amine A is ______.
Which of the following statement(s) is/are incorrect in case of Hofmann bromamide degradation?
Identify the product ‘C’ in the following reaction.
\[\ce{Aniline ->[(CH3CH)2O][Pyridine] A ->[Br2][CH3COOH] B ->[H^+ or OH^-] C}\]
Assertion: Amimonolysis of alkyl halides involves the reaction between alkyl halides and alcoholic ammonia.
Reason: Ammonolysis of alkyl halides produces secondary amines only.
