Question:

What is the product of the reaction between Benzene and \(CH_3Cl\) in the presence of anhydrous \(AlCl_3\)?

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Friedel–Crafts alkylation introduces an alkyl group onto a benzene ring using a Lewis acid catalyst like \(AlCl_3\).
Updated On: Apr 29, 2026
  • Toluene
  • Phenol
  • Chlorobenzene
  • Benzaldehyde
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The Correct Option is A

Solution and Explanation

Concept: This reaction is known as Friedel–Crafts Alkylation, where an alkyl group substitutes a hydrogen atom of the benzene ring in the presence of a Lewis acid catalyst such as \(AlCl_3\).

Step 1:
Formation of electrophile. In the presence of \(AlCl_3\), methyl chloride forms a methyl carbocation. \[ CH_3Cl + AlCl_3 \rightarrow CH_3^+ + AlCl_4^- \]

Step 2:
Electrophilic substitution on benzene. The methyl carbocation attacks the benzene ring, replacing one hydrogen atom. \[ C_6H_6 + CH_3^+ \rightarrow C_6H_5CH_3 \]

Step 3:
Product formation. The product formed is Toluene.
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