Question:

Acetophenone can be prepared from which of the following reactants? 

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Acetophenone can be synthesized via Grignard reaction with nitriles or Friedel-Crafts acylation using acetyl anhydride or acetyl chloride in the presence of AlCl\(_3\).
Updated On: Mar 26, 2025
  • B, D only
  • B, C, D only
  • A, C, D only
  • A, B, C only
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The Correct Option is A

Solution and Explanation

Acetophenone (C6H5COCH3) is a ketone that can be synthesized by various methods. Let's analyze each given reactant:

1. Option A (Benzoyl Chloride + CH3MgBr):
- Reaction with Grignard reagent would lead to a tertiary alcohol, not acetophenone.
- Incorrect for acetophenone synthesis.

2. Option B (Benzonitrile + CH3MgBr, H2O):
- Grignard reagents react with nitriles (-CN) to form ketones after hydrolysis.
- This is a correct method to form Acetophenone.

3. Option C (Benzoic Acid + CH3COOH):
- No ketone formation occurs directly between benzoic acid and acetic acid.
- Incorrect method for Acetophenone synthesis.

4. Option D (Benzene + Acetyl Anhydride [(CH3CO)2O]):
- This is Friedel-Crafts Acylation, which forms acetophenone in the presence of AlCl3.
- Correct method to form Acetophenone.

Thus, B and D are the correct choices.
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