
(a)
Interpretation:
The member that rapidly undergoes
Concept Introduction:
The
The first step of
Frist step is the slow step also rate determining step so the rate of the reaction is depends on the concentration of substrate only.
Nucleophile attacks the both front and back side of carbocation in
Order of the substrate that favored in
(a)

Answer to Problem 9.25P
The member that rapidly undergoes
Explanation of Solution
Given:
In
2-chloro-2 methyl propane gives more stable carbocation than 1-chlorobutane.
Hence, the member that rapidly undergoes
(b)
Interpretation:
The member that rapidly undergoes
Concept Introduction:
The rate of the reaction is depends on a single reactant in reaction is known as
The first step of
Frist step is the slow step also rate determining step so the rate of the reaction is depends on the concentration of substrate only.
Nucleophile attacks the both front and back side of carbocation in
Order of the substrate that favored in
(b)

Answer to Problem 9.25P
The member that rapidly undergoes
Explanation of Solution
Given:
Bromine is better leaving group than chlorine.
Hence, the member that rapidly undergoes
(c)
Interpretation:
The member that rapidly undergoes
Concept Introduction:
The rate of the reaction is depends on a single reactant in reaction is known as
The first step of
Frist step is the slow step also rate determining step so the rate of the reaction is depends on the concentration of substrate only.
Nucleophile attacks the both front and back side of carbocation in
Order of the substrate that favored in
(c)

Answer to Problem 9.25P
The member that rapidly undergoes
Explanation of Solution
Given:
In
Allyl cation is more stable than primary cation.
Hence, the member that rapidly undergoes
(d)
Interpretation:
The member that rapidly undergoes
Concept Introduction:
The rate of the reaction is depends on a single reactant in reaction is known as
The first step of
Frist step is the slow step also rate determining step so the rate of the reaction is depends on the concentration of substrate only.
Nucleophile attacks the both front and back side of carbocation in
Order of the substrate that favored in
(d)

Answer to Problem 9.25P
The member that rapidly undergoes
Explanation of Solution
Given:
In
Substuted allyllic cation is more stable than allylic cation.
Hence, the member that rapidly undergoes
(e)
Interpretation:
The member that rapidly undergoes
Concept Introduction:
The rate of the reaction is depends on a single reactant in reaction is known as
The first step of
Frist step is the slow step also rate determining step so the rate of the reaction is depends on the concentration of substrate only.
Nucleophile attacks the both front and back side of carbocation in
Order of the substrate that favored in
(e)

Answer to Problem 9.25P
The member that rapidly undergoes
Explanation of Solution
Given:
In
2-chloropentane gives more stable carbocation than 1-chloropentane.
Hence, the member that rapidly undergoes
(f)
Interpretation:
The member that rapidly undergoes
Concept Introduction:
The rate of the reaction is depends on a single reactant in reaction is known as
The first step of
Frist step is the slow step also rate determining step so the rate of the reaction is depends on the concentration of substrate only.
Nucleophile attacks the both front and back side of carbocation in
Order of the substrate that favored in
(f)

Answer to Problem 9.25P
The member that rapidly undergoes
Explanation of Solution
Given:
In
Allylic cation is more stable than vinyl cation.
Hence, the member that rapidly undergoes
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Chapter 9 Solutions
Organic Chemistry
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