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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Saved v Question: I've done both of the graphs and generated an equation from excel, I just need help explaining A-B. Below is just the information I used to get the graphs obtain the graph please help. Prepare two graphs, the first with the percent transmission on the vertical axis and concentration on the horizontal axis and the second with absorption on the vertical axis and concentration on the horizontal axis. Solution # Unknown Concentration (mol/L) Transmittance Absorption 9.88x101 635 0.17 1.98x101 47% 0.33 2.95x101 31% 0.51 3.95x10 21% 0.68 4.94x10 14% 24% 0.85 0.62 A.) Give an equation that relates either the % transmission or the absorption to the concentration. Explain how you arrived at your equation. B.) What is the relationship between the percent transmission and the absorption? C.) Determine the concentration of the ironlll) salicylate in the unknown directly from the graph and from the best fit trend-line (least squares analysis) of the graph that yielded a straight…

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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