Consider the following molecules:

The correct order of rate of hydrolysis is: [2025]
r > q > p > s
q > p > r > s
p > r > q > s
p > q > r > s
(4)
Hydrolysis of acid derivatives is a nucleophilic elimination reaction. For such reactions rate of reaction is acid chloride > anhydride > ester > amide.

Assertion A: Hydrolysis of an alkyl chloride is a slow reaction but in the presence of , the rate of the hydrolysis increases.
Reason R: is a good nucleophile as well as a good leaving group.
In the light of the above statements, choose the correct answer from the options given below: [2023]
A is false but R is true
A is true but R is false
Both A and R are true but R is NOT the correct explanation of A
Both A and R are true and R is the correct explanation of A
(4)
being a good nucleophile forms which gets hydrolysed readily.
The compound which will have the lowest rate towards nucleophilic aromatic substitution on treatment with is [2023]




(2)

Chlorobenzene with strong EWG (i.e., ) undergoes nucleophilic aromatic substitution at a faster rate with .
Decreasing order towards reaction for the following compounds is: [2023]

d > b > c > a
b > d > c > a
a > c > d > b
a > b > c > d
(2)
Rate of depends upon stability of carbocation.
The correct order of reactivity of following haloarenes towards nucleophilic substitution with aqueous NaOH is:

Choose the correct answer from the options given below: [2023]
D > C > B > A
A > B > D > C
C > A > D > B
D > B > A > C
(4)
Chlorobenzene undergoes aromatic nucleophilic substitution via carbanion intermediate. In such a reaction greater the –M group (–, –CN etc.) at o and p-position, greater the stability of carbanion intermediate and faster the rate of reaction.
Arrange the following compounds in increasing order of rate of aromatic electrophilic substitution reaction. [2023]

d, b, a, c
b, c, a, d
c, a, b, d
d, b, c, a
(3)
Due to increase in electron density in the ring, rate of increases, ERG increases the electron density.
Decreasing order of reactivity towards electrophilic substitution for the following compounds is: [2023]

a > d > e > b > c
d > a > e > c > b
e > d > a > b > c
c > b > a > d > e
(3)
Higher the electron density on benzene ring, higher is its reactivity towards electrophilic substitution reaction.
Hence, the correct order is
Correct statements for the given reaction are:

(A) Compound ‘B’ is aromatic
(B) The completion of above reaction is very slow
(C) ‘A’ shows tautomerism
(D) The bond length of C–C in compound B are found to be same
Choose the correct answer from the options given below: [2023]
A, C and D only
A, B and C only
A, B and D only
B, C and D only
(1)

Compound (A) shows tautomerism.
The correct order of reactivity of in methanol with the following nucleophiles is
[2026]
(3)
For the following given reaction

[X] & [Y] are-
Enantiomer of each other
Diastereomer of each other
Both are meso compounds
Constitutional isomer of each other
(2)
Diastereomer of each other

Most stable product of the above following reaction is




(2)
