Question:

Under what reaction conditions does the electrophilic chlorination of aromatic compounds usually occur?

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Lewis acid catalysts enhance electrophilic aromatic substitution reactions by activating halogens.
Updated On: Jun 8, 2025
  • \( \text{NaCl, CH}_3\text{OH} \)
  • \( \text{Cl}_2\text{AlCl}_3 \)
  • \( \text{Cl}_2\text{CCl}_4 \)
  • \( \text{NaCl, EtOH} \)
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The Correct Option is B

Solution and Explanation

Electrophilic chlorination of aromatic compounds is typically carried out using Cl\(_2\) with AlCl\(_3\) as a Lewis acid catalyst. AlCl\(_3\) polarizes Cl\(_2\), making it a stronger electrophile, enabling substitution on the benzene ring. Other options lack sufficient electrophilic activation for effective chlorination.
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