Organic Chemistry-Package(Custom)
Organic Chemistry-Package(Custom)
4th Edition
ISBN: 9781259141089
Author: SMITH
Publisher: MCG
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Chapter 24, Problem 24.28P
Interpretation Introduction

(a)

Interpretation: The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is to be drawn.

Concept introduction: Aldol reaction is the condensation reaction of the organic chemistry. In this reaction an enolate ion or an enol reacts with the carbonyl compound that leads to the formation of β-hydroxyaldehyde or β-hydroxyketone which on further dehydration gives the conjugated enone.

Expert Solution
Check Mark

Answer to Problem 24.28P

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is 3hydroxy2,2,4trimethylpentanal.

Organic Chemistry-Package(Custom), Chapter 24, Problem 24.28P , additional homework tip  1

Explanation of Solution

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is shown as,

Organic Chemistry-Package(Custom), Chapter 24, Problem 24.28P , additional homework tip  2

Figure 1

In this reaction, one molecule of isobutyraldehyde is treated with the strong base that leads to the formation of a resonance-stabilized enolate ion. Then, this enolate ion reacts with the second molecule of isobutyraldehyde followed by the hydrolysis to form 3hydroxy2,2,4trimethylpentanal as the desired product.

Conclusion

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is 3hydroxy2,2,4trimethylpentanal.

Interpretation Introduction

(b)

Interpretation: The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is to be drawn.

Concept introduction: Aldol reaction is the condensation reaction of the organic chemistry. In this reaction an enolate ion or an enol reacts with the carbonyl compound that leads to the formation of β-hydroxyaldehyde or β-hydroxyketone which on further dehydration gives the conjugated enone.

Expert Solution
Check Mark

Answer to Problem 24.28P

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is 3hydroxy2,2dimethylpropanal.

Organic Chemistry-Package(Custom), Chapter 24, Problem 24.28P , additional homework tip  3

Explanation of Solution

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is shown as,

Organic Chemistry-Package(Custom), Chapter 24, Problem 24.28P , additional homework tip  4

Figure 2

In this reaction, the compound, isobutyraldehyde is treated with the strong base that leads to the formation of a resonance-stabilized enolate ion. Then, this enolate ion reacts with formaldehyde followed by the hydrolysis to form 3hydroxy2,2dimethylpropanal as the desired product.

Conclusion

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is 3hydroxy2,2dimethylpropanal.

Interpretation Introduction

(c)

Interpretation: The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is to be drawn.

Concept introduction: Aldol reaction is the condensation reaction of the organic chemistry. In this reaction an enolate ion or an enol reacts with the carbonyl compound that leads to the formation of β-hydroxyaldehyde or β-hydroxyketone which on further dehydration gives the conjugated enone.

Expert Solution
Check Mark

Answer to Problem 24.28P

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is 2(hydroxy(phenyl)methyl)butanal.

Organic Chemistry-Package(Custom), Chapter 24, Problem 24.28P , additional homework tip  5

Explanation of Solution

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is shown as,

Organic Chemistry-Package(Custom), Chapter 24, Problem 24.28P , additional homework tip  6

Figure 3

In this reaction, the compound, butyraldehyde is treated with the strong base that leads to the formation of a resonance-stabilized enolate ion. Then, this enolate ion reacts with benzaldehyde followed by the hydrolysis to form 2(hydroxy(phenyl)methyl)butanal as the desired product.

Conclusion

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is 2(hydroxy(phenyl)methyl)butanal.

Interpretation Introduction

(d)

Interpretation: The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is to be drawn.

Concept introduction: Aldol reaction is the condensation reaction of the organic chemistry. In this reaction an enolate ion or an enol reacts with the carbonyl compound that leads to the formation of β-hydroxyaldehyde or β-hydroxyketone which on further dehydration gives the conjugated enone.

Expert Solution
Check Mark

Answer to Problem 24.28P

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is shown below.

Organic Chemistry-Package(Custom), Chapter 24, Problem 24.28P , additional homework tip  7

Explanation of Solution

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is shown as,

Organic Chemistry-Package(Custom), Chapter 24, Problem 24.28P , additional homework tip  8

Figure 4

In this reaction, one molecule of pentan-3-one is treated with the strong base that leads to the formation of a resonance-stabilized enolate ion. Then, this enolate ion reacts with the second molecule of pentan-3-one followed by the hydrolysis to form the desired β-hydroxyketone.

Conclusion

The product that is formed by the aldol reaction of the given starting material(s) by using OH, H2O is shown in Figure 4.

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Chapter 24 Solutions

Organic Chemistry-Package(Custom)

Ch. 24 - Prob. 24.11PCh. 24 - Prob. 24.12PCh. 24 - Prob. 24.13PCh. 24 - Prob. 24.14PCh. 24 - Problem 24.16 What ester is formed when each...Ch. 24 - What crossed Claisen product is formed from each...Ch. 24 - Prob. 24.17PCh. 24 - Draw the products of each reaction. a. b. Ch. 24 - Problem 24.20 Two steps in a synthesis of the...Ch. 24 - Prob. 24.20PCh. 24 - Problem 24.22 Which of the following compounds can...Ch. 24 - What product is formed when each pair of compounds...Ch. 24 - Problem 24.24 What starting materials are needed...Ch. 24 - Problem 24.25 Draw the products when each pair of...Ch. 24 - Problem 24.27 What starting materials are needed...Ch. 24 - Prob. 24.26PCh. 24 - 24.29 What steps are needed to convert A to B? Ch. 24 - Prob. 24.28PCh. 24 - Prob. 24.29PCh. 24 - 24.31 Draw the product formed in each directed...Ch. 24 - Prob. 24.31PCh. 24 - What starting materials are needed to synthesize...Ch. 24 - Prob. 24.33PCh. 24 - Prob. 24.34PCh. 24 - Prob. 24.35PCh. 24 - 24.36 Identify the structures of C and D in the...Ch. 24 - Prob. 24.37PCh. 24 - Prob. 24.38PCh. 24 - Prob. 24.39PCh. 24 - Draw the product formed from a Claisen reaction...Ch. 24 - Prob. 24.41PCh. 24 - 24.41 Even though B contains three ester groups, a...Ch. 24 - Prob. 24.43PCh. 24 - What starting materials are needed to prepare each...Ch. 24 - 24.44 Vetivone is isolated from vetiver, a...Ch. 24 - Draw the product of each Robinson annulation from...Ch. 24 - Prob. 24.47PCh. 24 - Draw the organic products formed when butanal...Ch. 24 - 24.47 Draw the organic products formed in each...Ch. 24 - 24.48 Fill in the lettered reagents needed for...Ch. 24 - Prob. 24.51PCh. 24 - Prob. 24.52PCh. 24 - Prob. 24.53PCh. 24 - Draw a stepwise mechanism for the following...Ch. 24 - Prob. 24.55PCh. 24 - Prob. 24.56PCh. 24 - Prob. 24.57PCh. 24 - Prob. 24.58PCh. 24 - Prob. 24.59PCh. 24 - Prob. 24.60PCh. 24 - Prob. 24.61PCh. 24 - Prob. 24.62PCh. 24 - Devise a synthesis of each compound from...Ch. 24 - Prob. 24.64PCh. 24 - Prob. 24.65PCh. 24 - Prob. 24.66PCh. 24 - 24.65 Answer the following questions about...Ch. 24 - Prob. 24.68PCh. 24 - Prob. 24.69PCh. 24 - Prob. 24.70PCh. 24 - Prob. 24.71PCh. 24 - 24.70 Draw a stepwise mechanism for the following...Ch. 24 - Prob. 24.73PCh. 24 - Prob. 24.74PCh. 24 - Prob. 24.75P
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