Give reasons for the following:
(i) Benzyl chloride is highly reactive towards the SN1 reaction.
(ii) 2-bromobutane is optically active but 1-bromobutane is optically inactive.
(iii) Electrophilic reactions in haloarenes occur slowly.
(i) The rate of reaction of SN1 reaction depends on stability of carbocation formed. The benzyl carbocation formed after removal of Cl is highly stabilized by resonance effect and thus, it is highly reactive towards the SN1 reaction.

(ii) 2-bromobutane is optically active but 1-bromobutane is optically inactive because 2-bromobutane have a chiral (all 4 groups attached to C* are different) carbon whereas 1-bromobutane is achiral.

(2-bromobutane)
(iii) In haloarenes, due to resonance the electron density increases on ortho and para position than at meta position. Further due to –I effect halogen has the tendency to withdraw electrons from benzene ring and hence the ring gets deactivated as compared to benzene. Hence, ESR of haloarenes occurs slowly.
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