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The most stable carbocation amongst the following is:

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$C H_{3} - \overset{\oplus}{C} = N H$

$C H_{3} \overset{\oplus}{C} H_{2}$

${(C H_{3})}_{2} - \underset{\oplus}{C} H$

$C H_{3} \overset{\oplus}{C} = O$

answer is C.

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Detailed Solution

The positively charged carbon atom in the carbocation is sp2 hybridised. This part of the carbocation is planar and the vacant p- orbital is perpendicular to this plane. The shape of methyl carbocation is trigonal planar.

A carbocation having plus I groups or electron donating groups will be more stable. Less electro negative elements will have more donating ability.

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