Aromatic aldehydes undergo disproportionation | vedclass

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Question

(B) The reaction described is the $Cannizzaro$ reaction. In this reaction,aldehydes that do not contain an $\alpha$-hydrogen atom undergo self-oxidati

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Cannizzaro reaction

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(B) The reaction described is the $Cannizzaro$ reaction. In this reaction,aldehydes that do not contain an $\alpha$-hydrogen atom undergo self-oxidation and reduction (disproportionation) in the presence of a concentrated alkali solution. For example,two molecules of benzaldehyde react with concentrated $NaOH$ to produce sodium benzoate and benzyl alcohol.

Aromatic aldehydes undergo disproportionation in the presence of concentrated sodium or potassium hydroxide to give the corresponding alcohol and acid salt. This reaction is known as:

Similar Questions

The reaction of phthalaldehyde with concentrated $NaOH$ produces:

For the reaction,the product expected is:

$R-C(=O)H + R-NH_2 \rightarrow R-CH=N-R$. This reaction gives the best yield at:

The above conversion can be achieved by:

Which of the following compounds will not undergo tautomerism?

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