$A$ carbanion acts as a:

  • A
    Base
  • B
    Nucleophile
  • C
    Both of the above
  • D
    None of the above

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Similar Questions

The correct order of decreasing stability of the following carbocations is:
$I. CH_3-CH^{+}-CH_3$
$II. CH_3-CH^{+}-OCH_3$
$III. CH_3-CH^{+}-CH_2-OCH_3$

Which of the following compounds gives the same carbocation on ionization?

Represent the structure of the free radical,carbocation,and carbanion derived from methane.

How many $1,2-$ shifts take place in the following carbocation to reach the most stable form?

Difficult
View Solution

Carbocation as an intermediate is likely to be formed in the reaction:

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