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The correct stability order of carbocations is

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Important Questions on Some Basic Principles of Organic Chemistry

EASY
The order of stability of the following carbocations:
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EASY
The lower stability of ethyl anion compared to methyl anion and the higher stability of ethyl radical compared to methyl radical, respectively, are due to
 
EASY
Which of the following is not a reaction intermediate?
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Choose the correct statement regarding the formation of carbocations A and B given :-

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In which of the following pairs A is more stable than B?
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The stability order of the above carbocations is 

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Arrange the following carbanions in order of their decreasing stability

(i) H3C-CC-

(ii) H-CC-

(iii) H3C-CH2-

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The compound that is most difficult to protonate is:
HARD

The major products A and B in the following reactions are

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EASY

 Arrange the following free radicals in order of decreasing stability:

MethylI, VinylII,AllylIII and benzyl(IV)

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In which of the following compounds, the C-Cl bond ionization shall give most stable carbonium ion?
EASY

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The correct order of stability of given carbocation is:

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Which of the following carbocations is most stable?

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Arrange the following carbocations in decreasing order of stability.

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EASY
For the following carbocations, the correct order of stability is
I. CH2-COCH3
II. CH2-OCH3
III. CH2-CH3
HARD
A solution of (-)1-chloro-1-phenylethane in toluene racemises slowly in the presence of a small amount of SbCl5, due to the formation of :