To predict the products of the following transesterification reaction. (a) ethyl benzoate + excess isopropanol + HCl Concept introduction: Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H 2 O . As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

Question

Want to see the full answer?

Answer 1

Question

Chapter 15.8, Problem 25P

(a)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(a) ethyl benzoate + excess isopropanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

(b)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(b) phenyl acetate + excess ethanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Reactions of carbonyl compounds with hydride ion donors. a. Draw reaction of an aldehyde with sodium borohydride forms a primary alcohol. b. Draw reaction of a ketone with sodium borohydride forms a secondary alcohol.

fill in the reagents а. b. OH + En

Compound that is most easily hydrolyzed by acid in water `NH A. В. F C. D.

Answer 2

Question

Chapter 15.8, Problem 25P

(a)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(a) ethyl benzoate + excess isopropanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

(b)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(b) phenyl acetate + excess ethanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 15.8, Problem 25P

(a)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(a) ethyl benzoate + excess isopropanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

(b)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(b) phenyl acetate + excess ethanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 15.8, Problem 25P

(a)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(a) ethyl benzoate + excess isopropanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

(b)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(b) phenyl acetate + excess ethanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 15.8, Problem 25P

(a)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(a) ethyl benzoate + excess isopropanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

(b)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(b) phenyl acetate + excess ethanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

Answer 6

Chapter 15.8, Problem 25P

(a)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(a) ethyl benzoate + excess isopropanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

Answer 7

Chapter 15.8, Problem 25P

(a)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(a) ethyl benzoate + excess isopropanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

Answer 8

(b)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(b) phenyl acetate + excess ethanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

Answer 9

(b)

Interpretation Introduction

Interpretation:

To predict the products of the following transesterification reaction.

(b) phenyl acetate + excess ethanol + HCl

Concept introduction:

Transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester. This is like hydrolysis of ester but here nucleophile is alcohol molecule instead of H2O. As alkoxide groups have same basicity, therefore, an excess amount of alcohol is used. The addition of an acid also increases the rate of reaction by protonating the carbonyl oxygen atom. A general transesterification is written as,

Answer 10

Expert Solution & Answer

Answer 11

Expert Solution & Answer

Answer 12

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 13

Ch. 15.1 - The aromas of many flowers and fruits are due to...Ch. 15.1 - Name the following:Ch. 15.1 - Prob. 3P Ch. 15.2 - Which is longer, the carbon-oxygen single bond in...Ch. 15.2 - There are three carbon-oxygen bonds in methyl...Ch. 15.2 - Prob. 6P Ch. 15.4 - a. What is the product of the reaction of acetyl...Ch. 15.4 - What is the product of an acyl substitution...Ch. 15.5 - a. Which compound has the stretching vibration for...Ch. 15.5 - Using the pKa values listed in Table 15.1, predict...

Solution Summary: The author explains that transesterification is the process of formation of a new ester molecule from the reaction of alcohol and an ester.

Concept explainers

Want to see the full answer?

Chapter 15 Solutions