Organic Chemistry
Organic Chemistry
5th Edition
ISBN: 9780078021558
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Chapter 23, Problem 23.47P
Interpretation Introduction

(a)

Interpretation: The products formed by the reaction of Na+CH(CO2Et)2 with the given electrophile followed by treatment with H2O are to be drawn.

Concept introduction: Nucleophilic addition reaction is a type of organic reaction in which the nucleophile is added to the electrophilic site. The carbon atom in carbonyl compound acts as an electrophilic centre where a nucleophile attacks and gives an addition product.

Expert Solution
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Answer to Problem 23.47P

The product formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O is diethyl 2-(2-hydroxypropyl)malonate.

Explanation of Solution

The given compound is,

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  1

Figure 1

The nucleophile CH(CO2Et)2 attacks on the electrophilic centre of the given compound and forms a product followed by hydrolysis. The final product is diethyl 2-(2-hydroxypropyl)malonate. The reaction is shown below.

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  2

Figure 2

On the further treatment of diethyl 2-(2-hydroxypropyl)malonate with water in the presence of heat, it forms derivative of carboxylic acid. The reaction is shown below.

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  3

Figure 3

Hence, the product formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O is diethyl 2-(2-hydroxypropyl)malonate. On further treatment of product with water in the presence of heat yields the derivative of carboxylic acid.

Conclusion

The product formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O is diethyl 2-(2-hydroxypropyl)malonate.

Interpretation Introduction

(b)

Interpretation: The products formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O are to be drawn.

Concept introduction: Nucleophilic addition reaction is a type of organic reaction in which the nucleophile is added to the electrophilic site. The carbon atom in carbonyl compound acts as an electrophilic centre where a nucleophile attacks and gives an addition product.

Expert Solution
Check Mark

Answer to Problem 23.47P

The product formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O is diethyl 2-(hydroxymethyl)malonate.On the further treatment of product with water in the presence of heat yields the derivative of carboxylic acid.

Explanation of Solution

The given compound is,

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  4

Figure 4

The nucleophile CH(CO2Et)2 attacks on the electrophilic centre of the given compound and forms a product followed by hydrolysis. The final product is diethyl 2-(hydroxymethyl)malonate. The reaction is shown below.

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  5

Figure 5

On the further treatment of diethyl 2-(hydroxymethyl)malonate with water in the presence of heat, it forms derivative of carboxylic acid. The reaction is shown below.

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  6

Figure 6

Hence, the product formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O is diethyl 2-(hydroxymethyl)malonate. On further treatment of product with water in the presence of heat yields derivative of carboxylic acid.

Conclusion

The product formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O is diethyl 2-(hydroxymethyl)malonate.

Interpretation Introduction

(c)

Interpretation: The products formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O are to be drawn.

Concept introduction: Nucleophilic addition reaction is a type of organic reaction in which the nucleophile is added to the electrophilic site. The carbon atom in carbonyl compound acts as an electrophilic centre where a nucleophile attacks and gives an addition product.

Expert Solution
Check Mark

Answer to Problem 23.47P

The product formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O is diethyl 2-acetylmalonate. On further treatment of product with water in the presence of heat yields the derivative of carboxylic acid.

Explanation of Solution

The given compound is,

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  7

Figure 7

The nucleophile CH(CO2Et)2 attacks on the electrophilic centre of the given compound and forms a product followed by hydrolysis. The final product is diethyl 2-acetylmalonate. The reaction is shown below.

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  8

Figure 8

On the further treatment of diethyl 2-acetylmalonate with water in the presence of heat, it forms derivative of carboxylic acid. The reaction is shown below.

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  9

Figure 9

Hence, the product formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O is diethyl 2-acetylmalonate. On further treatment of product with water in the presence of heat yields the derivative of carboxylic acid.

Conclusion

The product formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O is diethyl 2-acetylmalonate.

Interpretation Introduction

(d)

Interpretation: The product formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O is to be drawn.

Concept introduction: Nucleophilic addition reaction is a type of organic reaction in which the nucleophile is added to the electrophilic site. The carbon atom in carbonyl compound acts as an electrophilic centre where a nucleophile attacks and gives an addition product.

Expert Solution
Check Mark

Answer to Problem 23.47P

The products formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O are diethyl 2-acetylmalonate and ethanoic acid. On further treatment of product with water in the presence of heat yields the derivative of carboxylic acid.

Explanation of Solution

The given compound is,

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  10

Figure 10

The nucleophile CH(CO2Et)2 attacks on the electrophilic centre of the given compound and forms a product followed by hydrolysis. The final products are diethyl 2-acetylmalonate and ethanoic acid. The reaction is shown below.

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  11

Figure 11

On the further treatment of diethyl 2-acetylmalonate with water in the presence of heat, it forms derivative of carboxylic acid. The reaction is shown below.

Organic Chemistry, Chapter 23, Problem 23.47P , additional homework tip  12

Figure 12

Hence, the products formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O are diethyl 2-acetylmalonate and ethanoic acid. On further treatment of product with water in the presence of heat yields the derivative of carboxylic acid.

Conclusion

The products formed by the reaction of Na+CH(CO2Et)2 with given electrophile followed by treatment with H2O are diethyl 2-acetylmalonate and ethanoic acid.

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Chapter 23 Solutions

Organic Chemistry

Ch. 23 - Problem 23.11 Draw the products of each...Ch. 23 - Problem 23.12 Draw the products of each reaction....Ch. 23 - Prob. 23.13PCh. 23 - Prob. 23.14PCh. 23 - Prob. 23.15PCh. 23 - Prob. 23.16PCh. 23 - Prob. 23.17PCh. 23 - Problem 23.18 How can pentan-2-one be converted...Ch. 23 - Problem 23.19 Identify A, B, and C, intermediates...Ch. 23 - Problem 23.20 Which of the following compounds...Ch. 23 - Problem 23.21 Draw the products of each...Ch. 23 - Prob. 23.22PCh. 23 - Prob. 23.23PCh. 23 - Prob. 23.24PCh. 23 - Prob. 23.25PCh. 23 - Prob. 23.26PCh. 23 - Prob. 23.27PCh. 23 - Prob. 23.28PCh. 23 - 23.29 Draw enol tautomer(s) for each compound....Ch. 23 - 22.30 The cis ketone A is isomerized to a trans...Ch. 23 - 23.31 Draw enol tautomer(s) for each compound. ...Ch. 23 - Prob. 23.32PCh. 23 - Prob. 23.33PCh. 23 - Prob. 23.34PCh. 23 - 23.35 Rank the labeled protons in each compound in...Ch. 23 - Prob. 23.36PCh. 23 - Prob. 23.37PCh. 23 - 23.38 Acyclovir is an effective antiviral agent...Ch. 23 - 23.39 Explain why forms two different alkylation...Ch. 23 - Prob. 23.40PCh. 23 - 23.41 Acid-catalyzed bromination of pentanone ...Ch. 23 - 23.42 Draw a stepwise mechanism for the following...Ch. 23 - Prob. 23.43PCh. 23 - Prob. 23.44PCh. 23 - 23.45 Devise a synthesis of valproic acid , a...Ch. 23 - 23.46 Synthesize each compound from diethyl...Ch. 23 - Prob. 23.47PCh. 23 - Prob. 23.48PCh. 23 - Prob. 23.49PCh. 23 - 23.50 Draw the organic products formed in each...Ch. 23 - 23.51 Draw the products formed (including...Ch. 23 - Prob. 23.52PCh. 23 - Prob. 23.53PCh. 23 - 23.54 Clopidogrel is the generic name for Plavix,...Ch. 23 - 23.55 What reaction conditions—base, solvent, and...Ch. 23 - Prob. 23.56PCh. 23 - 23.57 Draw a stepwise mechanism showing how two...Ch. 23 - 23.58 Draw a stepwise mechanism for the following...Ch. 23 - Prob. 23.59PCh. 23 - 23.60 Draw stepwise mechanisms illustrating how...Ch. 23 - Prob. 23.61PCh. 23 - Prob. 23.62PCh. 23 - 23.63 Synthesize each compound from cyclohexanone...Ch. 23 - Prob. 23.64PCh. 23 - Prob. 23.65PCh. 23 - 23.66 Synthesize (Z)-hept-5-en-2-one from ethyl...Ch. 23 - Prob. 23.67PCh. 23 - 23.68 Capsaicin, the spicy component of hot...Ch. 23 - 23.69 Treatment of W with , followed by , affords...Ch. 23 - Prob. 23.70PCh. 23 - Prob. 23.71PCh. 23 - Prob. 23.72PCh. 23 - Prob. 23.73PCh. 23 - Prob. 23.74P
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