The correct option is C E2 eliminations are by the use of polar aprotic solvent and high concentration of a strong base
(a) First step in both SN1 and E1 involves dissociation of leaving group and formation of carbocation. Hence, the first step in the both SN1 and E1 reaction is same.
(b) A SN2 reaction proceeds with complete stereochemical inversion while SN1 reaction proceeds with racemisation.
(c) E2 reactions are favoured by polar aprotic solvents and rate of E2 reaction increases as the strength of base increases.
(d) A SN2 reaction proceeds with complete stereochemical inversion while SN1 reaction proceeds with racemisation.