Question

Of the two bromoderivatives, C6H5CH(CH3)Br and C6H5CH(C6H5)Br which one is more reactive in SN1 substitution reaction and why?

Answer 1

tertiary

Step-by-step explanation:

tertiary halogenoalkanes are more reactive than primary and secondary as the carbocation is more stable due to alkyl groups( have high electron density) donating electrons to stabilise the carbocation