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The Cannizzaro reaction is given by...

The Cannizzaro reaction is given by

A

benzaldehyde

B

acetaldehyde

C

acetone

D

trimethyl acetaldehyde

Text Solution

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The correct Answer is:
To answer the question regarding the Cannizzaro reaction, we need to identify which compounds can undergo this reaction. The Cannizzaro reaction occurs with aldehydes that do not have any alpha-hydrogens. Here’s a step-by-step solution: ### Step 1: Understand the Cannizzaro Reaction The Cannizzaro reaction is a redox reaction that involves the disproportionation of aldehydes that lack alpha-hydrogens. In this reaction, one molecule of the aldehyde is oxidized to a carboxylic acid, while another molecule is reduced to an alcohol. ### Step 2: Identify Aldehydes Without Alpha-Hydrogens To determine which compounds can undergo the Cannizzaro reaction, we need to check for the presence of alpha-hydrogens. An alpha-hydrogen is a hydrogen atom attached to the carbon adjacent to the carbonyl group (C=O). ### Step 3: Analyze the Given Options 1. **Benzaldehyde (C6H5CHO)**: - Structure: Benzaldehyde has a phenyl group (C6H5) attached to the carbonyl carbon. The carbon adjacent to the carbonyl (alpha carbon) has no hydrogens. - Conclusion: Benzaldehyde has no alpha-hydrogens and can undergo the Cannizzaro reaction. 2. **Acetaldehyde (CH3CHO)**: - Structure: Acetaldehyde has a methyl group (CH3) attached to the carbonyl carbon. The alpha carbon has three hydrogens. - Conclusion: Acetaldehyde has alpha-hydrogens and cannot undergo the Cannizzaro reaction. 3. **Acetone (CH3COCH3)**: - Structure: Acetone is a ketone with two methyl groups attached to the carbonyl carbon. The alpha carbons each have three hydrogens. - Conclusion: Acetone has alpha-hydrogens and cannot undergo the Cannizzaro reaction. 4. **Trimethylacetaldehyde (C(CH3)3CHO)**: - Structure: Trimethylacetaldehyde has three methyl groups attached to the alpha carbon adjacent to the carbonyl carbon. The alpha carbon has no hydrogens. - Conclusion: Trimethylacetaldehyde has no alpha-hydrogens and can undergo the Cannizzaro reaction. ### Step 4: Final Conclusion From the analysis above, the compounds that can undergo the Cannizzaro reaction are: - **Benzaldehyde** - **Trimethylacetaldehyde** ### Summary The Cannizzaro reaction is applicable to aldehydes without alpha-hydrogens. In the given options, Benzaldehyde and Trimethylacetaldehyde can undergo this reaction. ---
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Knowledge Check

  • Cannizzaro's reaction is given by

    A
    Formaldehyde
    B
    Acetaldehyde
    C
    Acetic acid
    D
    Acetone
  • Cannizzaro's reaction is

    A
    addition reaction
    B
    a disproportionation reaction
    C
    self oxidation reaction
    D
    Elimination reaction
  • Consider the following statements. Cannizzaro reaction is given by those aldehydes which do not have sigma-H atom. 2-methyl propanal undergoes both Aldol condensation and Cannizzaro reaction. Select the correct option

    A
    Only I
    B
    Only II
    C
    Both (1) and (2)
    D
    None of the above
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