Chemistry, asked by madiham3296, 9 months ago

Smith rearrangement carboxylic acid and their deriatives reats with hydozoic acid and further hydrolysis will provide primary amine

Answers

Answered by Anonymous

Explanation:

It is named after Karl Friedrich Schmidt (1887–1971), who first reported it in 1924 by successfully converting benzophenone and hydrazoic acid to benzanilide. ... The reaction is effective with carboxylic acids to give amines (above), and with ketones to give amides (below)

Answered by TheDreamCatcher

Answer:

The Schmidt reactions refer to the acid-catalyzed reactions of hydrazoic acid with electrophiles, such as carbonyl compounds, tertiary alcohols and alkenes. These substrates undergo rearrangement and extrusion of nitrogen to furnish amines, nitriles, amides or imines

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