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Q. Aryl halides doesn't undergo nucleophilic substitution reactions under ordinary conditions because of
1. approach of nucleophile is retarded
2. carbon carrying halogen atoms is $sp^3$ - hybridised
3. the substrate molecule is destabilised due to resonance
4. partial double bond character between carbon and halogen

KEAMKEAM 2010Haloalkanes and Haloarenes

Solution:

Because of the + R effect of halogen atom, $ CX $ bond of aryl halide has some double bond character, hence it is inert towards nucleophile and approach of nucleophile is retarded.