The correct option is C E2→ primary > secondary > tertiary
(a). The reactivity order of alkyl halide for SN1 reaction is depends on the stability of carbocation formed because the reaction goes through the carbocation intermediate.
Order of stability of carbocation is,
tertiary > secondary > primary
Therefore, the relative reactivity of alkyl halide for SN1 is,
tertiary > secondary > primary
(b). The reactivity of alkyl halide for E1 reaction is based on the stability of alkene formed. Tertiary alkyl halide form more stable alkene followed by secondary and at last primary.
So the correct order of reactivity for E1 reaction is,
tertiary > secondary > primary
(c). The reactivity of alkyl halide for E2 reaction is based on the stability of alkene formed. Tertiary alkyl halide form more stable alkene followed by secondary and at last primary.
So the correct order of reactivity for E2 reaction is,
tertiary > secondary > primary
(d). The SN2 reaction proceeds through transition state where the nucleophile will attact the akly halide at back position. Hence, less steric alkyl halide will undergo SN2 reaction fastly. Therefore, the relative reactivity of alkyl halide for SN2 is,
primary > secondary > tertiary
Thus, option (c) is the incorrect order.