Question:medium

Formaldehyde undergoes Cannizzaro reaction because
(A) It has alpha-hydrogen atom.
(B) It does not have alpha-hydrogen atom.
(C) It does not undergo self-oxidation and reduction on heating with concentrated alkali.
(D) It undergoes self-oxidation and reduction on heating with concentrated alkali.

Updated On: Jan 16, 2026
  • It does not have alpha-hydrogen atom

  • It has alpha-hydrogen atom

     

  • It does not undergo self-oxidation and reduction on heating with concentrated alkali
  • It undergoes self-oxidation and reduction on heating with concentrated alkali
Show Solution

The Correct Option is A

Solution and Explanation

The Cannizzaro reaction, a redox process, occurs when an aldehyde lacking an alpha-hydrogen atom reacts with a concentrated strong base, typically an alkali. The reaction proceeds as follows:

  • The aldehyde substrate must be devoid of an alpha-hydrogen atom.
  • Upon treatment with concentrated alkali, one aldehyde molecule is reduced to an alcohol, and another is oxidized to a carboxylate ion.
  • This reaction is exclusively applicable to aldehydes without alpha-hydrogen atoms; the presence of an alpha-hydrogen atom promotes enolization, leading to alternative reactions like aldol condensation.

Formaldehyde (HCHO) exemplifies an aldehyde that undergoes the Cannizzaro reaction due to its absence of an alpha-hydrogen atom, rendering it amenable to this specific reaction pathway.

Consequently, the rationale for this reaction is accurately stated as (A) It does not have an alpha-hydrogen atom.

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