Which of the following carbocations is most s | vedclass

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(D) The stability of a carbocation is increased by the presence of electron-donating groups that can stabilize the positive charge through resonance.I

Vedclass · Accepted Answer

$CH_3O-CH=CH-CH=CH^+$

Vedclass · Answer

(D) The stability of a carbocation is increased by the presence of electron-donating groups that can stabilize the positive charge through resonance.In the given options,the methoxy group $(-OCH_3)$ acts as a strong electron-donating group due to the $+M$ (mesomeric) effect.Among the options,the carbocation $CH_3O-CH=CH-CH=CH^+$ is the most stable because the positive charge is delocalized over a larger conjugated system,and the $+M$ effect of the $-OCH_3$ group is effectively transmitted through the extended conjugation to stabilize the carbocation.

Which of the following carbocations is most stable?

Similar Questions

The increasing order of stability of the following free radicals is:

Arrange the following cations in decreasing order of their stability:
$(a)$ $CH_3^+$
$(b)$ $F-CH_2-CH_2^+$
$(c)$ $Br-CH_2-CH_2^+$
$(d)$ $CH_3-CH_2-CH_2^+$

Which of the following is the most stable carbocation?

Which of the following represents the incorrect stability order?

The shape of a carbocation is:

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