Which of the following is the most correct el | vedclass

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(A) For a nucleophilic reaction to occur,the leaving group must depart,often facilitated by the formation of a stable carbocation. In the given molecu

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(A) For a nucleophilic reaction to occur,the leaving group must depart,often facilitated by the formation of a stable carbocation. In the given molecule,$CH_3-CH=CH-CH_2-Cl$,the departure of the $Cl^-$ ion is assisted by the resonance stabilization of the resulting carbocation. The $\pi$-electrons of the $C=C$ bond shift towards the $CH_2$ group,creating a positive charge on the carbon atom adjacent to the double bond,which is stabilized by the $+I$ effect of the $-CH_3$ group. This corresponds to the electron displacement shown in option $A$.

Which of the following is the most correct electron displacement for a nucleophilic reaction to take place?

Similar Questions

Which type of the overlap of orbitals is involved in hyperconjugation?

Identify the lowest positive charge developed (indicated by $\delta, \delta_1, \delta_2, \delta_3$) due to the inductive effect in the following compound: $CH_3-CH_2-CH_2-CH_2-Cl$.

What is the effect of electron displacement in a covalent bond?

$+I$ effect is shown by:

The correct stability order of the following species/molecules is:

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