Anyl halides are practically inert toward nucleophilic substitution reactions . The reasons for this fact areA. Because C -X bond has partial double bond character due to conjugation bewteen lone pair of X and `pi` electrons of aromatic ring .B. No `S_(N)1` reaction beacuase aryl carbocations are unstableC. No`S_(N)2` reaction because aromatic `pi` electron cloud do not allow backside attack of `Nu^(-)`D. Product obtained through nucleophilic substitution reactions are non aromatic

Anyl halides are practically inert toward nucleophilic substitution re

1.	Anyl halides are practically inert toward nucleophilic substitution reactions . The reasons for this fact areA. Because C -X bond has partial double bond character due to conjugation bewteen lone pair of X and `pi` electrons of aromatic ring .B. No `S_(N)1` reaction beacuase aryl carbocations are unstableC. No`S_(N)2` reaction because aromatic `pi` electron cloud do not allow backside attack of `Nu^(-)`D. Product obtained through nucleophilic substitution reactions are non aromatic
Answer» Correct Answer - (1,2,3)

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