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Question
The reaction of the bromo compound shown below with sodium ethoxide gives predominantly:
The reaction of the bromo compound shown below with sodium ethoxide gives predominantly:
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Solution
The correct option is C
In the above reaction, EtO− acts as a strong base and gives dehydrohalogenation type product via E2-elimination.
Cyclohexane and its derivatives are more preferred in the chair configuration.
D and Br are anti-periplanar to each other. So, E2-elimination is easy.
In the above reaction, EtO− acts as a strong base and gives dehydrohalogenation type product via E2-elimination.
Cyclohexane and its derivatives are more preferred in the chair configuration.
D and Br are anti-periplanar to each other. So, E2-elimination is easy.
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