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Non-reactivity of aryl halides towards nucleophilic substitution due to all the following except

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C-Cl bond has decreased bond energy in aryl halides

C - Cl bond acquires double bond character

Phenyl carbocation cannot stabilize through resonance

Difficult to replace -Cl group from more electro negative $s p^{2}$ carbon

answer is A.

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Detailed Solution

Resonance stabilization leading to C-Cl bond acquiring double bond character

B) C-Cl bond length is 169 pm which is much lesser C-Cl single bond (177 pm)

C) Difficult to replace -Cl group attached to more electronegative $s p^{2}$ carbon

Phenyl carbocation cannot stabilize through resonance

E) Phenyl group is electron rich and repels the incoming necleophile

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