EASY
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The decreasing order of nucleophilicity for the following anions is
(a)
(b)
(c)
(d)

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Important Questions on Organic Chemistry- Some Basic Principles and Techniques
MEDIUM
The correct order of nucleophilicity is

EASY
In electrophilic aromatic substitution reactions of chlorobenzene, the ortho/para-directing ability of chlorine is due to its

EASY
For the following reaction, identify the carbonyl compound that shows the highest reactivity.

EASY
Consider the following compounds

Hyperconjugation occurs in:

MEDIUM
The increasing order of nucleophilicity of the following nucleophiles is;


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

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

MEDIUM
Which of the following molecules is least resonance stabilized?

EASY
Which among the following is a set of nucleophiles?

EASY
The indicated atom is not a nucleophilic site in

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

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

EASY
In pyrrole, the electron density is maximum on


EASY
The order of stability of the following carbocations:


MEDIUM
In which of the following molecules, all atoms are coplanar?

MEDIUM
The stability of carbocations
follows the order

MEDIUM
The hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, due to

MEDIUM
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 statement regarding electrophiles is:

MEDIUM
The correct sequence of reagents for the following conversion will be


