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Introduction to Haloalkanes

The correct o...

Question

The correct order of stability of following carbocation :

A

A > B > C > D

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B

D > B > C > A

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C

D > C > B > A

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D

B > A > D > C

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Solution

The correct option is B D > B > C > A
R.E.F
$- I$ effect of $O -$ atom $∴$ Stability order $D > B > C > A$

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A carbocation is a group of atoms with a positively charged carbon atom having six electrons in the valence shell after sharing. Carbocations are formed in the heterolysis of a bond and are planar species. Stability of carbocation is determined by inductive effect, hyperconjugation and resonance effect. Greater the number of contributing structures more is the stability of a Carbocation. Electron releasing groups (+I effect) increases the stability of a carbocation whereas the electron withdrawing groups (I effect) have an opposite effect.

Which of the following is most stable carbocation?

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