(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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- Which one of the molecules shown below prefers to exist as its enol tautomer?arrow_forwardwhat is the major product of the SN1 OR SN2 structure below?arrow_forwardWhen bromomethane undergoes solvolysis in a solvent mixture composed of 90% water/10% acetone, the reaction rate is faster than when the same compound is solvolyzed in 80% water/20% acetone. Explain.arrow_forward
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- i need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,arrow_forwardWhich alkyl halide in each pair will undergo the faster SN2 reaction?arrow_forwardWhich of the following compounds (A or M) would be the better choice for a nucleophilic substitution reactionusing Compound T as the starting material and DMSO as the solvent? Would the resulting reaction be SN1 or SN2?arrow_forward
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