An equation for the preparation of the given compound from a suitable alcohol and a reactant molecule is to be written. Concept Introduction: Alkyl sulfonates are prepared by the reaction of an alcohol with sulfonyl chlorides. These reactions are carried out in suitable solvents such as trimethylamine, amines , etc. In these reactions, the hydrogen atom of the hydroxyl group in alcohols is substituted by the methyl sulfonate group. Their preparation involves the oxygen of the alcohol and not the carbon to which the oxygen is attached. If the structure for the product molecule is known, then the corresponding reactant alcohol can be found out by replacing the methyl sulfonate group by the hydrogen atom. The stereochemistry of the original alcohol and the carbon skeleton, both are maintained when the alcohols are converted to their corresponding alkyl sulfonates.

Question

Want to see the full answer?

Answer 1

Question

Chapter 5, Problem 38P

Interpretation Introduction

Interpretation:

An equation for the preparation of the given compound from a suitable alcohol and a reactant molecule is to be written.

Concept Introduction:

Alkyl sulfonates are prepared by the reaction of an alcohol with sulfonyl chlorides. These reactions are carried out in suitable solvents such as trimethylamine, amines, etc.

In these reactions, the hydrogen atom of the hydroxyl group in alcohols is substituted by the methyl sulfonate group.

Their preparation involves the oxygen of the alcohol and not the carbon to which the oxygen is attached.

If the structure for the product molecule is known, then the corresponding reactant alcohol can be found out by replacing the methyl sulfonate group by the hydrogen atom.

The stereochemistry of the original alcohol and the carbon skeleton, both are maintained when the alcohols are converted to their corresponding alkyl sulfonates.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Please help me with number 1-3. Thank you so much.

Draw the major product of this reaction ingnore the inorganic byproducts. 1. NaOCH2CH3 at 25 C 2. PhCH2Br (1 eq)

At 90ºC the vapor pressure of ortho-xylene is 20 kPa and that of meta-xylene is 18 kPa. What is the composition of the vapor in equilibrium with a mixture in which the mole fraction of o-xylene is 0.60?

Answer 2

Question

Chapter 5, Problem 38P

Interpretation Introduction

Interpretation:

An equation for the preparation of the given compound from a suitable alcohol and a reactant molecule is to be written.

Concept Introduction:

Alkyl sulfonates are prepared by the reaction of an alcohol with sulfonyl chlorides. These reactions are carried out in suitable solvents such as trimethylamine, amines, etc.

In these reactions, the hydrogen atom of the hydroxyl group in alcohols is substituted by the methyl sulfonate group.

Their preparation involves the oxygen of the alcohol and not the carbon to which the oxygen is attached.

If the structure for the product molecule is known, then the corresponding reactant alcohol can be found out by replacing the methyl sulfonate group by the hydrogen atom.

The stereochemistry of the original alcohol and the carbon skeleton, both are maintained when the alcohols are converted to their corresponding alkyl sulfonates.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 5, Problem 38P

Interpretation Introduction

Interpretation:

An equation for the preparation of the given compound from a suitable alcohol and a reactant molecule is to be written.

Concept Introduction:

Alkyl sulfonates are prepared by the reaction of an alcohol with sulfonyl chlorides. These reactions are carried out in suitable solvents such as trimethylamine, amines, etc.

In these reactions, the hydrogen atom of the hydroxyl group in alcohols is substituted by the methyl sulfonate group.

Their preparation involves the oxygen of the alcohol and not the carbon to which the oxygen is attached.

If the structure for the product molecule is known, then the corresponding reactant alcohol can be found out by replacing the methyl sulfonate group by the hydrogen atom.

The stereochemistry of the original alcohol and the carbon skeleton, both are maintained when the alcohols are converted to their corresponding alkyl sulfonates.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 5, Problem 38P

Interpretation Introduction

Interpretation:

An equation for the preparation of the given compound from a suitable alcohol and a reactant molecule is to be written.

Concept Introduction:

Alkyl sulfonates are prepared by the reaction of an alcohol with sulfonyl chlorides. These reactions are carried out in suitable solvents such as trimethylamine, amines, etc.

In these reactions, the hydrogen atom of the hydroxyl group in alcohols is substituted by the methyl sulfonate group.

Their preparation involves the oxygen of the alcohol and not the carbon to which the oxygen is attached.

If the structure for the product molecule is known, then the corresponding reactant alcohol can be found out by replacing the methyl sulfonate group by the hydrogen atom.

The stereochemistry of the original alcohol and the carbon skeleton, both are maintained when the alcohols are converted to their corresponding alkyl sulfonates.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 5, Problem 38P

Interpretation Introduction

Interpretation:

An equation for the preparation of the given compound from a suitable alcohol and a reactant molecule is to be written.

Concept Introduction:

Alkyl sulfonates are prepared by the reaction of an alcohol with sulfonyl chlorides. These reactions are carried out in suitable solvents such as trimethylamine, amines, etc.

In these reactions, the hydrogen atom of the hydroxyl group in alcohols is substituted by the methyl sulfonate group.

Their preparation involves the oxygen of the alcohol and not the carbon to which the oxygen is attached.

If the structure for the product molecule is known, then the corresponding reactant alcohol can be found out by replacing the methyl sulfonate group by the hydrogen atom.

The stereochemistry of the original alcohol and the carbon skeleton, both are maintained when the alcohols are converted to their corresponding alkyl sulfonates.

Answer 6

Chapter 5, Problem 38P

Interpretation Introduction

Interpretation:

An equation for the preparation of the given compound from a suitable alcohol and a reactant molecule is to be written.

Concept Introduction:

Alkyl sulfonates are prepared by the reaction of an alcohol with sulfonyl chlorides. These reactions are carried out in suitable solvents such as trimethylamine, amines, etc.

In these reactions, the hydrogen atom of the hydroxyl group in alcohols is substituted by the methyl sulfonate group.

Their preparation involves the oxygen of the alcohol and not the carbon to which the oxygen is attached.

If the structure for the product molecule is known, then the corresponding reactant alcohol can be found out by replacing the methyl sulfonate group by the hydrogen atom.

The stereochemistry of the original alcohol and the carbon skeleton, both are maintained when the alcohols are converted to their corresponding alkyl sulfonates.

Answer 7

Chapter 5, Problem 38P

Interpretation Introduction

Interpretation:

An equation for the preparation of the given compound from a suitable alcohol and a reactant molecule is to be written.

Concept Introduction:

Alkyl sulfonates are prepared by the reaction of an alcohol with sulfonyl chlorides. These reactions are carried out in suitable solvents such as trimethylamine, amines, etc.

In these reactions, the hydrogen atom of the hydroxyl group in alcohols is substituted by the methyl sulfonate group.

Their preparation involves the oxygen of the alcohol and not the carbon to which the oxygen is attached.

If the structure for the product molecule is known, then the corresponding reactant alcohol can be found out by replacing the methyl sulfonate group by the hydrogen atom.

The stereochemistry of the original alcohol and the carbon skeleton, both are maintained when the alcohols are converted to their corresponding alkyl sulfonates.

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. 5.1 - Prob. 1P Ch. 5.1 - Prob. 2P Ch. 5.1 - Many compounds contain more than one functional...Ch. 5.2 - Prob. 4P Ch. 5.3 - Prob. 5P Ch. 5.4 - Classify the isomeric C4H10O alcohols as being...Ch. 5.5 - Bromine is less electronegative than chlorine, yet...Ch. 5.6 - Prob. 8P Ch. 5.7 - Prob. 9P Ch. 5.8 - Prob. 10P

Solution Summary: The author explains that an equation for the preparation of the given compound from a suitable alcohol is to be written.

Concept explainers

Want to see the full answer?

Chapter 5 Solutions