Hydrolysis of CH3Br takes place much faster in presence of Nal because -
(a) I acts as good nucleophile as well as good leaving group.
(b) repusion between Brand Te is less.
(c) @OH is a good nucleophile.
Answers
Answered by
2
Answer:
A
Explanation:
Confirm Option A is the correct answer of this question
Answered by
2
Answer:
(a) I acts as good nucleophile as well as good leaving group...
Explanation:
a group which departed easily act as good leaving group..
and the strength of acid follows following order -
I >Br>Cl>F
remember F is a poor leaving group...
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