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How do you identify a strong electrophile?
Important Questions on Organic Chemistry- Some Basic Principles and Techniques
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In which of the following compounds, the bond ionization shall give most stable carbonium ion?

MEDIUM
The correct order of nucleophilicity is

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

HARD
The major products and in the following reactions are

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The increasing order of nucleophilicity of the following nucleophiles is;


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The compound that is most difficult to protonate is:

EASY
The order of stability of the following carbocations:


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 among the following is a set of nucleophiles?

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Given below are two statements :
Statement I : and both can generate nucleophile.
Statement II : and both will generate nitrile nucleophile with all reaction conditions.
Choose the most appropriate option :

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


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The correct sequence of reagents for the following conversion will be


EASY
The indicated atom is not a nucleophilic site in

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In which of the following pairs is more stable than

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

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

MEDIUM
The following compound
can readily be prepared by Williamson ether synthesis by reaction between

HARD
What will be the correct nucleophilicity order in protic or aprotic solvents?

EASY
The correct statement regarding electrophiles is:

EASY
Which of the following statements is not correct for a nucleophile?

