The correct option is A resonance stabilisation in aryl halide
In aryl halides, the reactivity of nucleophilic substitution reactions depends upon several factors such as the nature of leaving group, bond dissociation enthalpy of C−X bond, a solvent used. Whereas for alkyl halides carbon atoms to which halogen is attached is sp3 hybridized and hence lowers the dissociation enthalpy. Therefore due to resonance stabilization in aryl halide aryl halides are less reactive.