The possible structures for the products obtained from the reaction of benzaldehyde reacts with 1 , 2 − octanediol in benzene containing a small amount of p − toluenesulfonic acid is to be stated. Concept introduction: Carbonyl compounds react with diols to form acetals. This reaction is generally used as a way of protecting the carbonyl group in reactions. The carbonyl group can be generated back by hydrolysis of the acetal. Aldol condensation is a type of nucleophilic addition reaction that there must be at least one α hydrogen on one of the reactants.

Question

Want to see the full answer?

Answer 1

Question

Chapter 18, Problem 35P

Interpretation Introduction

Interpretation:

The possible structures for the products obtained from the reaction of benzaldehyde reacts with 1,2− octanediol in benzene containing a small amount of p− toluenesulfonic acid is to be stated.

Concept introduction:

Carbonyl compounds react with diols to form acetals. This reaction is generally used as a way of protecting the carbonyl group in reactions.

The carbonyl group can be generated back by hydrolysis of the acetal.

Aldol condensation is a type of nucleophilic addition reaction that there must be at least one α hydrogen on one of the reactants.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.

If possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.

Answer 2

Question

Chapter 18, Problem 35P

Interpretation Introduction

Interpretation:

The possible structures for the products obtained from the reaction of benzaldehyde reacts with 1,2− octanediol in benzene containing a small amount of p− toluenesulfonic acid is to be stated.

Concept introduction:

Carbonyl compounds react with diols to form acetals. This reaction is generally used as a way of protecting the carbonyl group in reactions.

The carbonyl group can be generated back by hydrolysis of the acetal.

Aldol condensation is a type of nucleophilic addition reaction that there must be at least one α hydrogen on one of the reactants.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 18, Problem 35P

Interpretation Introduction

Interpretation:

The possible structures for the products obtained from the reaction of benzaldehyde reacts with 1,2− octanediol in benzene containing a small amount of p− toluenesulfonic acid is to be stated.

Concept introduction:

Carbonyl compounds react with diols to form acetals. This reaction is generally used as a way of protecting the carbonyl group in reactions.

The carbonyl group can be generated back by hydrolysis of the acetal.

Aldol condensation is a type of nucleophilic addition reaction that there must be at least one α hydrogen on one of the reactants.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 18, Problem 35P

Interpretation Introduction

Interpretation:

The possible structures for the products obtained from the reaction of benzaldehyde reacts with 1,2− octanediol in benzene containing a small amount of p− toluenesulfonic acid is to be stated.

Concept introduction:

Carbonyl compounds react with diols to form acetals. This reaction is generally used as a way of protecting the carbonyl group in reactions.

The carbonyl group can be generated back by hydrolysis of the acetal.

Aldol condensation is a type of nucleophilic addition reaction that there must be at least one α hydrogen on one of the reactants.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 18, Problem 35P

Interpretation Introduction

Interpretation:

The possible structures for the products obtained from the reaction of benzaldehyde reacts with 1,2− octanediol in benzene containing a small amount of p− toluenesulfonic acid is to be stated.

Concept introduction:

Carbonyl compounds react with diols to form acetals. This reaction is generally used as a way of protecting the carbonyl group in reactions.

The carbonyl group can be generated back by hydrolysis of the acetal.

Aldol condensation is a type of nucleophilic addition reaction that there must be at least one α hydrogen on one of the reactants.

Answer 6

Chapter 18, Problem 35P

Interpretation Introduction

Interpretation:

The possible structures for the products obtained from the reaction of benzaldehyde reacts with 1,2− octanediol in benzene containing a small amount of p− toluenesulfonic acid is to be stated.

Concept introduction:

Carbonyl compounds react with diols to form acetals. This reaction is generally used as a way of protecting the carbonyl group in reactions.

The carbonyl group can be generated back by hydrolysis of the acetal.

Aldol condensation is a type of nucleophilic addition reaction that there must be at least one α hydrogen on one of the reactants.

Answer 7

Chapter 18, Problem 35P

Interpretation Introduction

Interpretation:

The possible structures for the products obtained from the reaction of benzaldehyde reacts with 1,2− octanediol in benzene containing a small amount of p− toluenesulfonic acid is to be stated.

Concept introduction:

Carbonyl compounds react with diols to form acetals. This reaction is generally used as a way of protecting the carbonyl group in reactions.

The carbonyl group can be generated back by hydrolysis of the acetal.

Aldol condensation is a type of nucleophilic addition reaction that there must be at least one α hydrogen on one of the reactants.

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. 18.1 - Prob. 1P Ch. 18.1 - Prob. 2P Ch. 18.3 - Prob. 3P Ch. 18.4 - Prob. 4P Ch. 18.4 - Prob. 5P Ch. 18.6 - Prob. 6P Ch. 18.7 - Prob. 7P Ch. 18.7 - Prob. 8P Ch. 18.7 - Prob. 9P Ch. 18.8 - Prob. 10P

Solution Summary: The author explains how benzaldehyde reacts with octanediol to form acetals. The alkene undergoes tautomerism to give a

Videos

Want to see the full answer?

Chapter 18 Solutions