Which compound out of the following pairs will react faster in SN1 reaction and
why ? CH2=CHBr or CH2=CHCHBr.
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Answer:
SN
1
reaction
Substitution Nucleophilic Unimolecular reaction:
It proceeds via the formation of a carbocation.
Reactivity towards SN
1
reaction depends upon the stability of carbocation and since tertiary carbocation is the most stable i.e, why tertiary halides show high reactivity towards SN
1
reaction.
Reactivity order of carbocation 3
∘
>2
∘
>1
∘
.
Therefore, this would undergo SN
1
reaction faster as it forms a 3
∘
carbocation.
Thus, the tert-butyl bromide will go S
N
1 reaction faster than ethyl bromide.
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