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-I Effect

Which of the ...

Question

Which of the following is the most stable carbocation intermediate?

\oplus C H_{2} - N H_{2}

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\oplus C H_{2} - O H

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\oplus C H_{2} - C l

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\oplus C H_{2} - {C H}_{3}

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Solution

The correct option is C $\oplus C H_{2} - N H_{2}$
Stability of carbocation is directly proportional to electron donating group.
As N and O has lone pair of electrons.

So, $\oplus C H_{2} - N H_{2} > \oplus C H_{2} - O H$
As electron donating power of $N H_{2}$ is higher than $O H$ .

Suggest Corrections

Similar questions

C H_{2} = C H - + C H_{2} and C H_{2} = C H - C H_{2} - + C H_{2}

C H_{3} - N H - + C H_{2} and + C H_{2} - O H

C H_{3} - O - C H_{2} - + C H_{2} and C H_{2} - O - + C H_{2}

C H_{3} - + C H - C H_{2} C H_{2} C H_{3} and C H_{3} C H_{2} - + C H - C H_{2} C H_{3}

C H_{3}

C H_{3}

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C H_{3} - C - C H_{2} - B r + N a O H ⟶ C H_{3} - C - C H_{2} - C H_{3}

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C H_{3}

O H

O H^{-}, N H_{2}^{-}, H C \equiv C^{⊝}

C H_{3} - C H_{2}^{⊝}

C H_{3} - C H_{2} - C l

C H_{3} - C H_{2} - C H_{2} - N H_{2}

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