Given below are the two statements regarding chlorobenzene
Statement I: Chlorobenzene is less reactive than benzene towards electrophilic substitution due to the -I effect of chlorine.
Statement II: Because of the -I effect of chlorine, it is a meta directing group.
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The -I effect reduces the electron density on the aromatic ring, making the ring less reactive in electrophilic substitution. Chlorine is meta-directing due to the combination of both the -I and +M effects, but the -I effect predominates in its deactivating influence.
Statement I is correct but statement II is not correct.
Statement I is not correct but statement II is correct.
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The Correct Option isC
Solution and Explanation
- Statement I is correct: Chlorobenzene is less reactive than benzene towards electrophilic substitution due to the -I effect of chlorine. Chlorine donates lone pair electrons to the aromatic ring through resonance, which decreases the electron density on the ring, making it less reactive.
- Statement II is incorrect: The -I effect of chlorine is deactivating and it directs incoming electrophiles to the meta position, but this is not because of the -I effect. The meta-directing property is due to the combination of the -I effect and the absence of a positive charge donation through resonance.