A way to carry out the given synthesis is to be proposed. Concept introduction: The Wolff–Kishner reduction converts the carbonyl ( C = O ) group of a ketone or aldehyde into a CH 2 group. Thus, a Wolff–Kishner reaction removes the C = O functional group of a ketone or aldehyde. For the given synthesis, we must use a carbon–carbon bond forming reaction. The reaction could be an α alkylation if we imagine one of the CH 2 groups being produced from a carbonyl group in a precursor. This reaction is carried out using retrosynthetic analysis.

Question

Want to see the full answer?

Answer 1

Question

Chapter 19, Problem 19.10P

Interpretation Introduction

Interpretation:

A way to carry out the given synthesis is to be proposed.

Concept introduction:

The Wolff–Kishner reduction converts the carbonyl ( $C = O$ ) group of a ketone or aldehyde into a $CH2$ group. Thus, a Wolff–Kishner reaction removes the $C = O$ functional group of a ketone or aldehyde. For the given synthesis, we must use a carbon–carbon bond forming reaction. The reaction could be an $α$ alkylation if we imagine one of the $CH2$ groups being produced from a carbonyl group in a precursor. This reaction is carried out using retrosynthetic analysis.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Firefly luciferin exhibits three rings. Identify which of the rings are aromatic. Identify which lone pairs are involved in establishing aromaticity. The lone pairs are labeled A-D below.

What is the [OH⁻] of a 1.80 M solution of pyridine (C₅H₅N, Kb = 1.70 × 10⁻⁹)?

What is the percent ionization in a 0.260 M solution of formic acid (HCOOH) (Ka = 1.78 × 10⁻⁴)?

Answer 2

Question

Chapter 19, Problem 19.10P

Interpretation Introduction

Interpretation:

A way to carry out the given synthesis is to be proposed.

Concept introduction:

The Wolff–Kishner reduction converts the carbonyl ( $C = O$ ) group of a ketone or aldehyde into a $CH2$ group. Thus, a Wolff–Kishner reaction removes the $C = O$ functional group of a ketone or aldehyde. For the given synthesis, we must use a carbon–carbon bond forming reaction. The reaction could be an $α$ alkylation if we imagine one of the $CH2$ groups being produced from a carbonyl group in a precursor. This reaction is carried out using retrosynthetic analysis.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 19, Problem 19.10P

Interpretation Introduction

Interpretation:

A way to carry out the given synthesis is to be proposed.

Concept introduction:

The Wolff–Kishner reduction converts the carbonyl ( $C = O$ ) group of a ketone or aldehyde into a $CH2$ group. Thus, a Wolff–Kishner reaction removes the $C = O$ functional group of a ketone or aldehyde. For the given synthesis, we must use a carbon–carbon bond forming reaction. The reaction could be an $α$ alkylation if we imagine one of the $CH2$ groups being produced from a carbonyl group in a precursor. This reaction is carried out using retrosynthetic analysis.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 19, Problem 19.10P

Interpretation Introduction

Interpretation:

A way to carry out the given synthesis is to be proposed.

Concept introduction:

The Wolff–Kishner reduction converts the carbonyl ( $C = O$ ) group of a ketone or aldehyde into a $CH2$ group. Thus, a Wolff–Kishner reaction removes the $C = O$ functional group of a ketone or aldehyde. For the given synthesis, we must use a carbon–carbon bond forming reaction. The reaction could be an $α$ alkylation if we imagine one of the $CH2$ groups being produced from a carbonyl group in a precursor. This reaction is carried out using retrosynthetic analysis.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 19, Problem 19.10P

Interpretation Introduction

Interpretation:

A way to carry out the given synthesis is to be proposed.

Concept introduction:

The Wolff–Kishner reduction converts the carbonyl ( $C = O$ ) group of a ketone or aldehyde into a $CH2$ group. Thus, a Wolff–Kishner reaction removes the $C = O$ functional group of a ketone or aldehyde. For the given synthesis, we must use a carbon–carbon bond forming reaction. The reaction could be an $α$ alkylation if we imagine one of the $CH2$ groups being produced from a carbonyl group in a precursor. This reaction is carried out using retrosynthetic analysis.

Answer 6

Chapter 19, Problem 19.10P

Interpretation Introduction

Interpretation:

A way to carry out the given synthesis is to be proposed.

Concept introduction:

The Wolff–Kishner reduction converts the carbonyl ( $C = O$ ) group of a ketone or aldehyde into a $CH2$ group. Thus, a Wolff–Kishner reaction removes the $C = O$ functional group of a ketone or aldehyde. For the given synthesis, we must use a carbon–carbon bond forming reaction. The reaction could be an $α$ alkylation if we imagine one of the $CH2$ groups being produced from a carbonyl group in a precursor. This reaction is carried out using retrosynthetic analysis.

Answer 7

Chapter 19, Problem 19.10P

Interpretation Introduction

Interpretation:

A way to carry out the given synthesis is to be proposed.

Concept introduction:

The Wolff–Kishner reduction converts the carbonyl ( $C = O$ ) group of a ketone or aldehyde into a $CH2$ group. Thus, a Wolff–Kishner reaction removes the $C = O$ functional group of a ketone or aldehyde. For the given synthesis, we must use a carbon–carbon bond forming reaction. The reaction could be an $α$ alkylation if we imagine one of the $CH2$ groups being produced from a carbonyl group in a precursor. This reaction is carried out using retrosynthetic analysis.

Answer 8

Expert Solution & Answer

Answer 9

Expert Solution & Answer

Answer 10

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 11

Ch. 19 - Prob. 19.1P Ch. 19 - Prob. 19.2P Ch. 19 - Prob. 19.3P Ch. 19 - Prob. 19.4P Ch. 19 - Prob. 19.5P Ch. 19 - Prob. 19.6P Ch. 19 - Prob. 19.7P Ch. 19 - Prob. 19.8P Ch. 19 - Prob. 19.9P Ch. 19 - Prob. 19.10P

Want to see the full answer?

Chapter 19 Solutions