Question:

Which of the following reagents are used in Friedel–Crafts alkylation?

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Remember the difference: Friedel–Crafts alkylation: Alkyl halide \(+\) \( \text{AlCl}_3 \) Friedel–Crafts acylation: Acyl chloride (\(RCOCl\)) \(+\) \( \text{AlCl}_3 \)
Updated On: Apr 20, 2026
  • \( \text{AlCl}_3 \)
  • \( \text{FeCl}_3 \)
  • \( \text{RCOCl} \)
  • \( \text{H}_2\text{SO}_4 \)
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The Correct Option is A

Solution and Explanation

Concept: Friedel–Crafts alkylation is an electrophilic aromatic substitution reaction in which an alkyl group is introduced into an aromatic ring. The reaction generally uses:
• An alkyl halide (\(R-X\))
• A Lewis acid catalyst The most commonly used Lewis acid catalyst is \( \text{AlCl}_3 \).

Step 1:
Role of the Lewis acid catalyst. The Lewis acid catalyst \( \text{AlCl}_3 \) helps generate the electrophile from the alkyl halide. Example: \[ R-Cl + AlCl_3 \rightarrow R^+ + AlCl_4^- \] The carbocation \(R^+\) then attacks the aromatic ring.

Step 2:
Examine the options.
• \( \text{AlCl}_3 \): Lewis acid catalyst used in Friedel–Crafts alkylation.
• \( \text{FeCl}_3 \): Commonly used in halogenation of benzene.
• \( \text{RCOCl} \): Used in Friedel–Crafts acylation, not alkylation.
• \( \text{H}_2\text{SO}_4 \): Used in nitration and sulfonation reactions.

Step 3:
Identify the correct reagent. Thus, the reagent used in Friedel–Crafts alkylation is \[ \boxed{\text{AlCl}_3} \]
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