Organic Chemistry
Organic Chemistry
4th Edition
ISBN: 9780073402772
Author: Janice G. Smith
Publisher: MCG
bartleby

Concept explainers

bartleby

Videos

Textbook Question
Book Icon
Chapter 29, Problem 29.37P

What is the predominant form of each of the following amino acids at pH = 1 ? What is the overall charge on the amino acid at this pH ? (a) threonine; (b) methionine; (c) aspartic acid; (d) arginine

Expert Solution
Check Mark
Interpretation Introduction

(a)

Interpretation: The predominant form of threonine at pH=1 and the overall charge on it at this pH is to be predicted.

Concept introduction: At isoelectric point, the amino acids exist in their neutral form. The amine groups exists as N+H3 and carboxyl groups as COO. The overall charge on an amino acid at isoelectric point is 0.

Answer to Problem 29.37P

The predominant form of threonine at pH=1 is,

Organic Chemistry, Chapter 29, Problem 29.37P , additional homework tip  1

The overall charge on it is +1.

Explanation of Solution

At isoelectric point, the amino acids exist in their neutral form. The amine groups exists as N+H3 and carboxyl groups as COO. However, when the pH of solution goes below isoelectric point, the amine group and carboxyl group exists as N+H3 and COOH, respectively.

The isoelectric point of threonine is 5.60. Therefore, the predominant form of threonine at pH=1 is,

Organic Chemistry, Chapter 29, Problem 29.37P , additional homework tip  2

Figure 1

The overall charge on threonine at pH=1 is +1.

Conclusion

The predominant form of threonine at pH=1 is shown in Figure 1 and the overall charge on it is +1.

Expert Solution
Check Mark
Interpretation Introduction

(b)

Interpretation: The predominant form of methionine at pH=1 and the overall charge on it at this pH is to be predicted.

Concept introduction: At isoelectric point, the amino acids exist in their neutral form. The amine groups exists as N+H3 and carboxyl groups as COO. The overall charge on an amino acid at isoelectric point is 0.

Answer to Problem 29.37P

The predominant form of methionine at pH=1 is

Organic Chemistry, Chapter 29, Problem 29.37P , additional homework tip  3

The overall charge on it is +1.

Explanation of Solution

At isoelectric point, the amino acids exist in their neutral form. The amine groups exists as N+H3 and carboxyl groups as COO. However, when the pH of solution goes below isoelectric point, the amine group and carboxyl group exists as N+H3 and COOH, respectively.

The isoelectric point of methionine is 5.74. Therefore, the predominant form of methionine at pH=1 is,

Organic Chemistry, Chapter 29, Problem 29.37P , additional homework tip  4

Figure 2

The overall charge on methionine at pH=1 is +1.

Conclusion

The predominant form of methionine at pH=1 is shown in Figure 2 and the overall charge on it is +1.

Expert Solution
Check Mark
Interpretation Introduction

(c)

Interpretation: The predominant form of aspartic acid at pH=1 and the overall charge on it at this pH is to be predicted.

Concept introduction: At isoelectric point, the amino acids exist in their neutral form. The amine groups exists as N+H3 and carboxyl groups as COO. The overall charge on an amino acid at isoelectric point is 0.

Answer to Problem 29.37P

The predominant form of aspartic acid at pH=1 is,

Organic Chemistry, Chapter 29, Problem 29.37P , additional homework tip  5

The overall charge on it is +1.

Explanation of Solution

At isoelectric point, the amino acids exist in their neutral form. The amine groups exists as N+H3 and carboxyl groups as COO. However, when the pH of solution goes below isoelectric point, the amine group and carboxyl group exists as N+H3 and COOH, respectively.

The isoelectric point of aspartic acid is 2.98. Therefore, the predominant form of aspartic acid at pH=1 is,

Organic Chemistry, Chapter 29, Problem 29.37P , additional homework tip  6

Figure 3

The overall charge on aspartic acid at pH=1 is +1.

Conclusion

The predominant form of aspartic acid at pH=1 is shown in Figure 3 and the overall charge on it is +1.

Expert Solution
Check Mark
Interpretation Introduction

(d)

Interpretation: The predominant form of arginine at pH=1 and the overall charge on it at this pH is to be predicted.

Concept introduction: At isoelectric point, the amino acids exist in their neutral form. The amine groups exists as N+H3 and carboxyl groups as COO. The overall charge on an amino acid at isoelectric point is 0.

Answer to Problem 29.37P

The predominant form of arginine at pH=1 is,

Organic Chemistry, Chapter 29, Problem 29.37P , additional homework tip  7

The overall charge on it is +3.

Explanation of Solution

At isoelectric point, the amino acids exist in their neutral form. The amine groups exists as N+H3 and carboxyl groups as COO. However, when the pH of solution goes below isoelectric point, the amine group and carboxyl group exists as N+H3 and COOH, respectively.

The isoelectric point of arginine is 10.76. Therefore, the predominant form of arginine at pH=1 is,

Organic Chemistry, Chapter 29, Problem 29.37P , additional homework tip  8

Figure 4

The overall charge on arginine at pH=1 is +3.

Conclusion

The predominant form of arginine at pH=1 is shown in Figure 4 and the overall charge on it is +3.

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
What is the predominant form of the following amino acids at pH= 1? What is the overall charge on the amino acid at this pH? arginine
What is the predominant form of the following amino acids at pH= 1? What is the overall charge on the amino acid at this pH? threonine
What is the predominant form of the following amino acids at pH= 1? What is the overall charge on the amino acid at this pH? methionine

Chapter 29 Solutions

Organic Chemistry

Ch. 29 - Prob. 29.11PCh. 29 - Problem 29.13 What alkene is needed to synthesize...Ch. 29 - Problem 29.14 Draw the structure of each peptide....Ch. 29 - Name each peptide using both the one-letter and...Ch. 29 - Prob. 29.15PCh. 29 - Prob. 29.16PCh. 29 - Problem 29.18 Glutathione, a powerful antioxidant...Ch. 29 - Problem 29.19 Draw the structure of the...Ch. 29 - Problem 29.20 Give the amino acid sequence of an...Ch. 29 - a What products are formed when each peptide is...Ch. 29 - Prob. 29.21PCh. 29 - Devise a synthesis of each peptide from amino acid...Ch. 29 - Devise a synthesis of the following dipeptide from...Ch. 29 - Prob. 29.24PCh. 29 - Consider two molecules of a tetrapeptide composed...Ch. 29 - What types of stabilizing interactions exist...Ch. 29 - Prob. 29.27PCh. 29 - Draw the product formed when the following amino...Ch. 29 - With reference to the following peptide: a...Ch. 29 - Devise a synthesis of the following dipeptide from...Ch. 29 - Prob. 29.31PCh. 29 - Prob. 29.32PCh. 29 - Histidine is classified as a basic amino acid...Ch. 29 - Tryptophan is not classified as a basic amino acid...Ch. 29 - What is the structure of each amino acid at its...Ch. 29 - To calculate the isoelectric point of amino acids...Ch. 29 - What is the predominant form of each of the...Ch. 29 - 29.37 What is the predominant form of each of the...Ch. 29 - a. Draw the structure of the tripeptide A–A–A, and...Ch. 29 - Draw the organic product formed when the amino...Ch. 29 - 29.39 Draw the organic products formed in each...Ch. 29 - 29.40 What alkyl halide is needed to synthesize...Ch. 29 - 29.41 Devise a synthesis of threonine from diethyl...Ch. 29 - 29.42 Devise a synthesis of each amino acid from...Ch. 29 - Prob. 29.45PCh. 29 - Prob. 29.46PCh. 29 - Prob. 29.47PCh. 29 - Prob. 29.48PCh. 29 - Prob. 29.49PCh. 29 - 29.48 Brucine is a poisonous alkaloid obtained...Ch. 29 - Prob. 29.51PCh. 29 - Prob. 29.52PCh. 29 - Draw the structure for each peptide: (a) Phe–Ala;...Ch. 29 - 29.52 For the tetrapeptide Asp–Arg–Val–Tyr: a....Ch. 29 - Prob. 29.55PCh. 29 - Explain why a peptide CN bond is stronger than an...Ch. 29 - Prob. 29.57PCh. 29 - 29.55 Draw the amino acids and peptide fragments...Ch. 29 - Prob. 29.59PCh. 29 - Prob. 29.60PCh. 29 - Prob. 29.61PCh. 29 - 29.59 An octapeptide contains the following amino...Ch. 29 - Prob. 29.63PCh. 29 - Prob. 29.64PCh. 29 - Draw all the steps in the synthesis of each...Ch. 29 - 29.62 Write out the steps for the synthesis of...Ch. 29 - 29.64 Another method to form a peptide bond...Ch. 29 - Prob. 29.68PCh. 29 - Prob. 29.69PCh. 29 - Which of the following amino acids are typically...Ch. 29 - After the peptide chain of collagen has been...Ch. 29 - Prob. 29.72PCh. 29 - Prob. 29.73PCh. 29 - 29.70 The anti-obesity drug orlistat works by...Ch. 29 - Prob. 29.75P
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
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
Text book image
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Biomolecules - Protein - Amino acids; Author: Tutorials Point (India) Ltd.;https://www.youtube.com/watch?v=ySNVPDHJ0ek;License: Standard YouTube License, CC-BY