why are aryl halides less reactive towards nucleophilic substitution reactions than alkyl halides
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why are aryl halides less reactive towards nucleophilic substitution reactions than alkyl halides ?
Aryl halides are more stable and less reactive due to resonance where the lone pair of electrons are in conjugation with a pie bond whereas in alkyl halides the carbon halogen bond is a sigma bond making aryl halides more stable than alkyl halides.
- So the bond energy between C-Cl increases so reactivity decrease.
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