Cannizzaro's reaction is followed by those aldehydes which ______ α-hydrogen atom.
A
have
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B
do not have
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C
have α hydroxy group with
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D
have α halogen with
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Solution
The correct option is B do not have The Cannizzaro reaction is a chemical reaction that involves the base-induced disproportionation of an aldehyde lacking a hydrogen atom in the alpha position.
The reaction involves a nucleophilic acyl substitution on an aldehyde, with the leaving group concurrently attacking another aldehyde in the second step.
First, hydroxide attacks a carbonyl. The resulting tetrahedral intermediate then collapses, re-forming the carbonyl and transferring hydride to attack another carbonyl.