Organic Chemistry (Looseleaf) - With Access
Organic Chemistry (Looseleaf) - With Access
4th Edition
ISBN: 9780077707316
Author: SMITH
Publisher: MCG
bartleby

Concept explainers

bartleby

Videos

Textbook Question
Book Icon
Chapter 22, Problem 22.75P

Devise a synthesis of each labeled compound using H 2 18 O and CH 3 13 CH 2 OH as the only sources of labeled starting materials. You may use any other unlabeled organic compounds and inorganic reagents.

a. Chapter 22, Problem 22.75P, Devise a synthesis of each labeled compound using H218O and CH313CH2OH as the only sources of , example  1 b. Chapter 22, Problem 22.75P, Devise a synthesis of each labeled compound using H218O and CH313CH2OH as the only sources of , example  2 c. Chapter 22, Problem 22.75P, Devise a synthesis of each labeled compound using H218O and CH313CH2OH as the only sources of , example  3 d. Chapter 22, Problem 22.75P, Devise a synthesis of each labeled compound using H218O and CH313CH2OH as the only sources of , example  4

Expert Solution
Check Mark
Interpretation Introduction

(a)

Interpretation:

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is to be stated.

Concept introduction:

The replacement or substitution of one functional group with another functional group in any chemical reaction is termed as substitution reaction. The electron rich chemical species that contains negative charge or lone pair of electrons is known as a nucleophile. In nucleophilc acyl substitution reaction, a nucleophile takes the position of a leaving group.

Answer to Problem 22.75P

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is,

Organic Chemistry (Looseleaf) - With Access, Chapter 22, Problem 22.75P , additional homework tip  1

Explanation of Solution

An ester is formed by the reaction of carboxylic acid with alcohol. This reaction is known as Fischer Esterification. During this reaction, bond formation between carbon and oxygen takes place and water removes as a byproduct. In the synthesis of given compound, acetic acid is used as the source of unlabeled carbon atom and CH313CH2OH as the source of labeled carbon atom as shown in Figure 1.

Organic Chemistry (Looseleaf) - With Access, Chapter 22, Problem 22.75P , additional homework tip  2

Figure 1

Conclusion

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is shown in Figure 1.

Expert Solution
Check Mark
Interpretation Introduction

(b)

Interpretation:

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is to be stated.

Concept introduction:

The replacement or substitution of one functional group with another functional group in any chemical reaction is termed as substitution reaction. The electron rich chemical species that contains negative charge or lone pair of electrons is known as a nucleophile. In nucleophilc acyl substitution reaction, a nucleophile takes the position of a leaving group.

Answer to Problem 22.75P

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is,

Organic Chemistry (Looseleaf) - With Access, Chapter 22, Problem 22.75P , additional homework tip  3

Explanation of Solution

An ester is formed by the reaction of carboxylic acid with alcohol. This reaction is known as Fischer Esterification. During this reaction, bond formation between carbon and oxygen takes place and water removes as a byproduct. In the synthesis of given compound, CH313CH2OH is first converted to CH313COOH in the presence of Na2Cr2O7. Ethanol on reaction with CH313COOH leads to the formation of desired compound as shown in Figure 2.

Organic Chemistry (Looseleaf) - With Access, Chapter 22, Problem 22.75P , additional homework tip  4

Figure 2

Conclusion

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is shown in Figure 2.

Expert Solution
Check Mark
Interpretation Introduction

(c)

Interpretation:

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is to be stated.

Concept introduction:

The replacement or substitution of one functional group with another functional group in any chemical reaction is termed as substitution reaction. The electron rich chemical species that contains negative charge or lone pair of electrons is known as a nucleophile. In nucleophilc acyl substitution reaction, a nucleophile takes the position of a leaving group.

Answer to Problem 22.75P

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is,

Organic Chemistry (Looseleaf) - With Access, Chapter 22, Problem 22.75P , additional homework tip  5

Explanation of Solution

An ester is formed by the reaction of carboxylic acid with alcohol. This reaction is known as Fischer Esterification. During this reaction, bond formation between carbon and oxygen takes place and water removes as a byproduct. In the synthesis of given compound, diethylether is first hydrolyzed to give CH3CH218OH. Acetic acid undergoes Esterification with CH3CH218OH and leads to the formation of desired compound as shown in Figure 3.

Organic Chemistry (Looseleaf) - With Access, Chapter 22, Problem 22.75P , additional homework tip  6

Figure 3

Conclusion

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is shown in Figure 3.

Expert Solution
Check Mark
Interpretation Introduction

(d)

Interpretation:

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is to be stated.

Concept introduction:

The replacement or substitution of one functional group with another functional group in any chemical reaction is termed as substitution reaction. The electron rich chemical species that contains negative charge or lone pair of electrons is known as a nucleophile. In nucleophilc acyl substitution reaction, a nucleophile takes the position of a leaving group.

Answer to Problem 22.75P

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is,

Organic Chemistry (Looseleaf) - With Access, Chapter 22, Problem 22.75P , additional homework tip  7

Explanation of Solution

An ester is formed by the reaction of carboxylic acid with alcohol. This reaction is known as Fischer Esterification. During this reaction, bond formation between carbon and oxygen takes place and water removes as a byproduct. In the synthesis of given compound, CH313CH2OH is first convert to CH313CH218OH in a two step reaction. This product is then converted to CH313C18OOH which undergoes Esterification reaction with unlabeled ethanol to give desired product as shown below.

Organic Chemistry (Looseleaf) - With Access, Chapter 22, Problem 22.75P , additional homework tip  8

Figure 4

Conclusion

The synthesis of given compound by the use of H218O and CH313CH2OH as the only source of labeled staring materials is shown in Figure 4.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Devise a synthesis of each compound from aniline (C6H5NH2) as starting material.
Devise a synthesis of each compound. You may use HC ≡ CH, ethylene oxide, and alkyl halides as organic starting materials and any inorganic reagents.
Devise a synthesis of each compound from phenol (C6H5OH) and any other organic or inorganic reagents.

Chapter 22 Solutions

Organic Chemistry (Looseleaf) - With Access

Ch. 22 - Prob. 22.11PCh. 22 - Prob. 22.12PCh. 22 - Prob. 22.13PCh. 22 - Prob. 22.14PCh. 22 - Problem 22.15 Draw the products of each...Ch. 22 - Problem 22.16 Draw the products of each reaction. ...Ch. 22 - Prob. 22.17PCh. 22 - Problem 22.18 Draw a stepwise mechanism for the...Ch. 22 - Prob. 22.19PCh. 22 - Problem 22.20 Fenofibrate is a...Ch. 22 - Problem 22.21 What product is formed when the...Ch. 22 - How would you synthesize olestra from sucrose? Ch. 22 - What is the composition of the soap prepared by...Ch. 22 - Problem 22.24 Draw a stepwise mechanism for the...Ch. 22 - Prob. 22.25PCh. 22 - Problem 22.26 Some penicillins cannot be...Ch. 22 - Prob. 22.27PCh. 22 - Prob. 22.28PCh. 22 - Prob. 22.29PCh. 22 - Problem 22.30 Glucosamine is a dietry supplement...Ch. 22 - Draw the products of each reaction. a. c. b.Ch. 22 - Draw a tautomer of each compound.Ch. 22 - Draw the product of each reaction. a.b.Ch. 22 - Draw the product of each reaction. a. b.Ch. 22 - Prob. 22.35PCh. 22 - Problem 22.36 Outline two different ways that can...Ch. 22 - 22.37 Rank the following compounds in order of...Ch. 22 - Prob. 22.38PCh. 22 - Prob. 22.39PCh. 22 - Prob. 22.40PCh. 22 - Give thestructure corresponding to each name. a....Ch. 22 - Prob. 22.42PCh. 22 - Prob. 22.43PCh. 22 - 22.43 Explain why is a stronger acid and a weaker...Ch. 22 - Draw the product formed when pentanoyl chloride...Ch. 22 - Draw the product formed when pentanoic anhydride...Ch. 22 - Draw the product formed when phenylacetic acid is...Ch. 22 - Prob. 22.48PCh. 22 - Prob. 22.49PCh. 22 - Draw the product formed when phenylacetonitrile ...Ch. 22 - Prob. 22.51PCh. 22 - Prob. 22.52PCh. 22 - Prob. 22.53PCh. 22 - Prob. 22.54PCh. 22 - Prob. 22.55PCh. 22 - Prob. 22.56PCh. 22 - Draw a stepwise mechanism for each reaction. a. b.Ch. 22 - When acetic acid CH3COOH is treated with a trace...Ch. 22 - Prob. 22.59PCh. 22 - Prob. 22.60PCh. 22 - Prob. 22.61PCh. 22 - Prob. 22.62PCh. 22 - Prob. 22.63PCh. 22 - Draw a stepwise mechanism for the following...Ch. 22 - 22.63 Acid-catalyzed hydrolysis of forms compound...Ch. 22 - Prob. 22.66PCh. 22 - Devise a synthesis of each compound using...Ch. 22 - Convert 1-bromohexane (CH3CH2CH2CH2CH2CH2Br) into...Ch. 22 - Prob. 22.69PCh. 22 - Prob. 22.70PCh. 22 - Prob. 22.71PCh. 22 - Prob. 22.72PCh. 22 - Prob. 22.73PCh. 22 - Prob. 22.74PCh. 22 - Devise a synthesis of each labeled compound using...Ch. 22 - 22.70 What polyester or poly amide can be prepared...Ch. 22 - 22.71 What two monomers are needed to prepare each...Ch. 22 - Prob. 22.78PCh. 22 - How can IR spectroscopy be used to distinguish...Ch. 22 - Rank the compounds in each group in order of...Ch. 22 - 22.75 Identify the structures of each compound...Ch. 22 - 22.76 Identify the structures of A and B, isomers...Ch. 22 - Prob. 22.83PCh. 22 - 22.78 Identify the structure of compound C...Ch. 22 - 22.79 Identify the structures of D and E, isomers...Ch. 22 - 22.80 With reference to amides A and B, the...Ch. 22 - Prob. 22.87PCh. 22 - Prob. 22.88PCh. 22 - Prob. 22.89PCh. 22 - Draw a stepwise mechanism for the following...Ch. 22 - Draw a stepwise mechanism for the following...
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY
Nomenclature: Crash Course Chemistry #44; Author: CrashCourse;https://www.youtube.com/watch?v=U7wavimfNFE;License: Standard YouTube License, CC-BY