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B
It forms carbine or substituted carbine
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C
Two atoms are removed from α and β positions
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D
In CHCl3;α elimination is not possible
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Solution
The correct option is A It forms carbine or substituted carbine α elimination (eliminations in which both the proton and the leaving
group are located on the same atom) follow a mechanism akin to an E1cB
β-elimination. A strong base removes an acidic proton adjacent to an
electron withdrawing group to give a carbanion. Loss of a leaving group
from the carbanion creates a carbene. One of the best known elimination
reactions occurs when chloroform is treated with base, forming a
dichlorocarbene.