Which of the following most readily undergoes an E2 reaction with sodium ethoxide (NaOCH2CH3)?A) (CH3)CF.
1 answer:
Answer:
(CH3)CI
Explanation:
As we move down the group, the halogen atoms become more easily polarizable and the C-X bond is more easily broken.
Recall that E2 mechanism has to do with synchronous proton abstraction and loss of the halogen.
These occur faster with (CH3)CI than when the C-X bond involves other halogens.
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