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

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asked Jan 4, 2021 83.0k views

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Andy Harvey · Answer 1 · 2021-01-09T22:31:38+0000

Answer:

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

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

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