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(B) The reactivity of the $C-X$ bond towards nucleophilic substitution depends on the strength of the $C-X$ bond. In $CH_2=CH-Cl$ (Vinyl chloride) and

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Chlorobenzene,Vinyl chloride,Chloroethane

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(B) The reactivity of the $C-X$ bond towards nucleophilic substitution depends on the strength of the $C-X$ bond. In $CH_2=CH-Cl$ (Vinyl chloride) and $C_6H_5-Cl$ (Chlorobenzene),the $C-X$ bond acquires partial double bond character due to resonance,making it stronger and less reactive. In $CH_3-CH_2-Cl$ (Chloroethane),the $C-X$ bond is a pure single bond,making it the most reactive. Comparing Vinyl chloride and Chlorobenzene,the $C-Cl$ bond in vinyl chloride is generally considered less reactive than in chlorobenzene due to the specific hybridization and resonance effects. Thus,the increasing order of reactivity is: $Chlorobenzene < Vinyl chloride < Chloroethane$.

The set of compounds in which the reactivity of the halogen atom increases in the order is ..........

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