(i) → (b) (ii) → (d) (iii) → (e) (iv) → (a) (v) → (c)

The first reaction is an electrophilic substitution reaction where Cl⁺ from Cl₂ and FeCl₃ complex attacks the benzene ring and carry out the substitution.

The second reaction is an electrophilic addition reaction where HBr is added across the double bond following Markownikoff’s rule.

The third reaction is a nucleophilic substitution reaction following the S_N1 mechanism where the –I group is replaced by –OH group.

The fourth reaction is a nucleophilic aromatic substitution reaction where the –Cl group is replaced by –OH.

The fifth reaction is a dehydrohalogenation reaction where the alkyl halide follows Saytzeff elimination reaction.