The following carbocation is stabilized by th | vedclass

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Question

(A) The given carbocation is the $1-$phenylethyl cation $(C_6H_5-CH^+-CH_3)$.This carbocation is stabilized by two main effects:$1$. Resonance: The em

Vedclass · Accepted Answer

filled $\sigma$ and filled $\pi$ orbitals

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(A) The given carbocation is the $1-$phenylethyl cation $(C_6H_5-CH^+-CH_3)$.This carbocation is stabilized by two main effects:$1$. Resonance: The empty $p$ orbital on the carbocation carbon interacts with the filled $\pi$ orbitals of the benzene ring, allowing delocalization of the positive charge.$2$. Hyperconjugation: The empty $p$ orbital on the carbocation carbon interacts with the filled $\sigma$ orbitals (specifically the $C-H$ $\sigma$ bonds of the adjacent methyl group).Therefore, the stabilization occurs through the interaction of the empty $p$ orbital with filled $\sigma$ and filled $\pi$ orbitals.

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

Similar Questions

Consider the following carbocations. What is the relative stability order of these carbocations?
$(1)$ $CH_3O-C_6H_4-CH_2^+$
$(2)$ $C_6H_5-CH_2^+$
$(3)$ $CH_3-C_6H_4-CH_2^+$

State whether the following statements are True or False:
$(i)$ $CH_3-CH_2^+$ is more stable than $CH_3^+$
$(ii)$ $CH_3-CH_2^+$ is less stable than $CH_3^+$
$(iii)$ $(CH_3)_3C^+$ is less stable than $CH_3^+$
$(iv)$ $(CH_3)_3C^+$ is more stable than $CH_3^+$

The stable carbocation formed in the reaction of benzene with $n$-propyl chloride in the presence of anhydrous $AlCl_3$ is:

Homolytic fission of $C-C$ bond in ethane gives an intermediate in which carbon is

Which of the following carbanions is the most stable?

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