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Byju's Answer
Standard XII
Chemistry
Chlorination
Which of the ...
Question
Which of the following compounds will react faster?
C
H
3
C
H
2
B
r
or
C
H
3
C
H
2
I
with
N
a
O
H
in ethanol________.
A
C
H
3
C
H
2
I
>
C
H
3
C
H
2
B
r
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B
C
H
3
C
H
2
I
<
C
H
3
C
H
2
B
r
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C
C
H
3
C
H
2
I
=
C
H
3
C
H
2
B
r
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D
None of these
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Solution
The correct option is
A
C
H
3
C
H
2
I
>
C
H
3
C
H
2
B
r
Solvents that can donate Hydrogen bonds (
−
O
H
or
−
N
H
)slow
S
N
2
reaction by associating with reactants.
Energy is required to break interactions between reactant and solvent.
But there is no need to consider the effect of solvent as l
arger halide ions are better leaving group.
Iodoalkanes
(
R
−
I
)
react more rapidly than bromoalkanes
(
R
−
B
r
)
.
Hence, the correct option is A.
Suggest Corrections
0
Similar questions
Q.
Which of the following compounds will react faster?
C
H
3
C
H
2
B
r
or
C
H
3
C
H
2
I
with
N
a
O
H
in acetone.
Q.
Which of the following compounds will react faster with
C
H
3
C
H
2
B
r
in ethanol ?
C
H
3
S
−
or
C
H
3
O
−
Q.
Arrange the following compounds in increasing order of their boiling points.
I.
C
H
3
C
H
2
C
H
2
B
r
II.
C
H
3
C
H
2
C
H
2
C
H
2
B
r
III.
(
C
H
3
)
2
C
H
C
H
2
B
r
IV.
(
C
H
3
)
3
C
B
r
Q.
C
H
3
−
C
|
C
H
3
=
C
H
2
H
B
r
−
−−−−
→
p
e
r
o
x
i
d
e
C
H
3
−
C
|
C
H
3
H
−
C
H
2
B
r
The intermediate of this reaction is?
Q.
Which of the following compounds will give racemic mixture of nucleophilic substitution by
O
H
−
ion?
(i)
C
H
3
−
C
H
|
C
2
H
5
−
B
r
(ii)
C
H
3
−
B
r
|
C
|
C
2
H
5
−
C
H
3
(iii)
C
H
3
−
C
H
|
C
2
H
5
−
C
H
2
B
r
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