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प्रश्न
In order to prepare a 1° amine from an alkyl halide with simultaneous addition of one \[\ce{CH2}\] group in the carbon chain, the reagent used as source of nitrogen is ______.
विकल्प
Sodium amide, \[\ce{NaNH2}\]
Sodium azide, \[\ce{NaN3}\]
Potassium cyanide, \[\ce{KCN}\]
Potassium phthalimide, \[\ce{C6H4 (CO)2N– K+}\]
उत्तर
In order to prepare a 1° amine from an alkyl halide with simultaneous addition of one \[\ce{CH2}\] group in the carbon chain, the reagent used as source of nitrogen is Potassium cyanide, \[\ce{KCN}\].
Explanation:
Potassium cyanide, as cyanide on reduction with sodium metal in alcohol, produces amine with increased carbon atoms.
\[\ce{R - X ->[KCN - KX] R - CN ->[Na/C2H2OH] R - CH2NH2}\]
APPEARS IN
संबंधित प्रश्न
Write the reactions of aromatic with nitrous acid.
Write the order of reactivity of alkyl halides with ammonia.
Which of the following reactions is appropriate for converting benzamide to aniline?
Identify product B in the following reaction.
\[\ce{Aniline ->[NaNO2][HCl] A ->[KI] B}\]
Amongst the given set of reactants, the most appropriate for preparing 2° amine is ______.
A compound 'A' on reduction with iron scrap and hydrochloric acid gives compound 'B' with molecular formula C6H7N. Compound 'B' on reaction with CHCl3 and alcoholic KOH produces an obnoxious smell of carbylamine due to the formation of 'C'. Identify 'A', 'B' and 'C' and write the chemical reactions involved.
Give reasons for the following:
Ammonolysis of alkyl halides is not a good method to prepare pure primary amines.
Which of the following would not be a good choice for reducing nitrobenzene to aniline?
Write short note on the following:
Ammonolysis
Write a short note on Ammonolysis.