a) Interpretation: The preparation of the compound shown using acetoacetic ester synthesis is to be given. Concept introduction: Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S N 2 attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation. To give: The preparation of the compound shown using acetoacetic ester synthesis.

Question

Please correct answer and don't use hand rating

Answer 1

Question

Chapter 22.SE, Problem 45AP

Interpretation Introduction

a)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Interpretation Introduction

b)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Students have asked these similar questions

Please correct answer and don't use hand rating

None

Draw Newman projects for each of the following molecules with 3 different rotational angles from carbon 2 to carbon 3. Rank your structures from lowest to highest energy. What causes the energy differences? Label the overlap. a. b. Br OH C. Br Br

Answer 2

Question

Chapter 22.SE, Problem 45AP

Interpretation Introduction

a)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Interpretation Introduction

b)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 3

Question

Chapter 22.SE, Problem 45AP

Interpretation Introduction

a)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Interpretation Introduction

b)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 4

Question

Chapter 22.SE, Problem 45AP

Interpretation Introduction

a)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Interpretation Introduction

b)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 5

Chapter 22.SE, Problem 45AP

Interpretation Introduction

a)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Interpretation Introduction

b)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Answer 6

Chapter 22.SE, Problem 45AP

Interpretation Introduction

a)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Answer 7

Chapter 22.SE, Problem 45AP

Interpretation Introduction

a)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Answer 8

Interpretation Introduction

b)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Answer 9

Interpretation Introduction

b)

Interpretation:

The preparation of the compound shown using acetoacetic ester synthesis is to be given.

Concept introduction:

Acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons. The methyl ketone part comes from acetoacetic eater while the remaining carbon comes from the primary alkyl halide. The reaction occurs in three steps i) enolate ion formation ii) S_N² attack of the enolate anion on the alkyl halide iii) hydrolysis and decarboxylation.

To give:

The preparation of the compound shown using acetoacetic ester synthesis.

Answer 10

Expert Solution & Answer

Answer 11

Expert Solution & Answer

Answer 12

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 13

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 14

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 15

Trending nowThis is a popular solution!

Answer 16

Trending nowThis is a popular solution!

Answer 17

Trending nowThis is a popular solution!

Answer 18

Trending now

Answer 19

This is a popular solution!

Answer 20

See solution

Check out sample textbook solution

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

Solution Summary: The author explains how acetoacetic ester synthesis converts an alkyl halide in to a methyl ketone having three more carbons.

Chapter 22 Solutions