a) Interpretation: Using an alkylation reaction as the key step how the compound shown can be prepared is to be given. Concept introduction: An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone , ester or nitrile by a S N 2 reaction of the enolate ion with an alkyl halide . Thus by looking at Î±- carbon of the product, the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA). To give: Using an alkylation reaction as the key step how to prepare the compound shown.

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Answer 1

Question

Chapter 22.7, Problem 16P

Interpretation Introduction

a)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared is to be given.

Concept introduction:
An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product, the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).
To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

b)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

c)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.
Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a^SN²reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

d)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

e)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

f)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

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(11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B Bond A Bond C a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. Weakest Bond Strongest Bond b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. c. (5pts) Use principles discussed in lecture, supported by relevant structures, to succinctly explain the why your part b (i) radical is more stable than your part b(ii) radical. Written explanation can be no more than one-two succinct sentence(s)!

Answer 2

Question

Chapter 22.7, Problem 16P

Interpretation Introduction

a)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared is to be given.

Concept introduction:
An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product, the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).
To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

b)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

c)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.
Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a^SN²reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

d)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

e)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

f)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

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Answer 3

Question

Chapter 22.7, Problem 16P

Interpretation Introduction

a)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared is to be given.

Concept introduction:
An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product, the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).
To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

b)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

c)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.
Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a^SN²reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

d)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

e)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

f)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

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Answer 4

Question

Chapter 22.7, Problem 16P

Interpretation Introduction

a)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared is to be given.

Concept introduction:
An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product, the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).
To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

b)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

c)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.
Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a^SN²reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

d)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

e)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

f)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Expert Solution & Answer

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Answer 5

Chapter 22.7, Problem 16P

Interpretation Introduction

a)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared is to be given.

Concept introduction:
An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product, the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).
To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

b)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

c)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.
Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a^SN²reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

d)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

e)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Interpretation Introduction

f)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 6

Chapter 22.7, Problem 16P

Interpretation Introduction

a)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared is to be given.

Concept introduction:
An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product, the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).
To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 7

Chapter 22.7, Problem 16P

Interpretation Introduction

a)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared is to be given.

Concept introduction:
An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product, the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).
To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 8

Interpretation Introduction

b)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 9

Interpretation Introduction

b)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 10

Interpretation Introduction

c)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.
Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a^SN²reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 11

Interpretation Introduction

c)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.
Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a^SN²reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 12

Interpretation Introduction

d)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 13

Interpretation Introduction

d)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 14

Interpretation Introduction

e)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 15

Interpretation Introduction

e)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 16

Interpretation Introduction

f)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 17

Interpretation Introduction

f)

Interpretation:

Using an alkylation reaction as the key step how the compound shown can be prepared.

Concept introduction:

An alkylation reaction is used to introduce a methyl or a primary alkyl group in Î±- position of a ketone, ester or nitrile by a ^SN² reaction of the enolate ion with an alkyl halide. Thus by looking at Î±- carbon of the product the alkyl halide to be used in the reaction can be identified. The enolate ion can be produced by using lithium diisopropylamide (LDA).

To give:

Using an alkylation reaction as the key step how to prepare the compound shown.

Answer 18

Expert Solution & Answer

Answer 19

Expert Solution & Answer

Answer 20

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Answer 21

Ch. 22.1 - Prob. 1P Ch. 22.1 - How many acidic hydrogens does each of the...Ch. 22.1 - Prob. 3P Ch. 22.3 - Write the complete mechanism for the deuteration...Ch. 22.3 - Prob. 5P Ch. 22.4 - If methanol rather than water is added at the end...Ch. 22.5 - Prob. 7P Ch. 22.5 - Draw a resonance structure of the acetonitrile...Ch. 22.6 - If methanol rather than water is added at the end...Ch. 22.7 - Prob. 10P

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Chapter 22 Solutions