Which of the following intermediates is more | vedclass

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(C) The given intermediates are carbanions stabilized by resonance within the benzene ring. An electron-withdrawing group $(EWG)$ like $-NO_2$ increas

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(C) The given intermediates are carbanions stabilized by resonance within the benzene ring. An electron-withdrawing group $(EWG)$ like $-NO_2$ increases the stability of a carbanion by dispersing the negative charge through the inductive and resonance effects. This stabilization is most effective when the $-NO_2$ group is at the ortho or para position relative to the negative charge,as the negative charge can be delocalized directly onto the oxygen atoms of the nitro group. In option $C$,the $-NO_2$ group is at the para position,providing maximum stabilization compared to the meta position (option $B$) or no substituent (option $A$). Therefore,the intermediate in option $C$ is the most stable.

Which of the following intermediates is more stable?

Similar Questions

Stability order of the following carbocations is:
$(i)$ $CH_3-C^{+}(CH_3)-CH_2-CH_3$
$(ii)$ $CH_3-CH^{+}-CH_3$
$(iii)$ $CH_3-C^{+}(CH_3)-CH_3$
$(iv)$ $Ph-CH^{+}-CH_3$

In the organic reaction by fission of bond,which intermediate species are formed? Name these species and explain their stability.

The following carbocation is stabilized by the interaction of the empty $p$ orbital with:

Number of carbocations from the following that are not stabilized by hyperconjugation is $...........$ .

Which of the following is most likely to undergo a favorable hydride shift?

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