Anyl halides are practically inert toward nucleophilic substitution reactions . The reasons for this fact are

Options

A. 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 unstable
C. 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

(1,2,3)