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Question

Friedel-Craft's reaction using MeCl and anhydrous AlCl3 will take place most efficiently with:

A
benzene
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B
nitrobenzene
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C
acetophenone
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D
toluene
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Solution

The correct option is D toluene
Friedel-crafts reaction is an electrophile substitution reaction and presence of an electron-releasing substituent like Methyl makes the benzene nucleus more reactive towards such reaction
The nitro-benzene has electron withdrawing groups which makes it less reactive than benzene.

Thus toluene is most reactive among the given.

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