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Which of the following carbocation would have the greatest stability?
(a)
(b)
(c)
(d)

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Important Questions on Basic Principles of Organic Chemistry
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

HARD
The major products and in the following reactions are

EASY
For the following carbocations, the correct order of stability is
I.
II.
III.

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Which of the following carbocations is most stable?

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

EASY
Which of the following is not a reaction intermediate?

EASY
The correct order of stability for the following alkoxides is:


EASY
The correct order of stability of given carbocation is:

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The stability of carbocations
follows the order

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In which of the following pairs is more stable than

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The stability order of the above carbocations is

EASY
The order of stability of the following carbocations:


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Choose the correct statement regarding the formation of carbocations A and B given :-

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Arrange the following carbanions in order of their decreasing stability
(i)
(ii)
(iii)

EASY
Arrange the following free radicals in order of decreasing stability:

EASY
The decreasing order of the stability of the following carbocations is

EASY
The most stable carbocation among the following is

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The compound that is most difficult to protonate is:

HARD
A solution of in toluene racemises slowly in the presence of a small amount of SbCl5, due to the formation of :

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Arrange the following compounds in order of decreasing acidity :


