Organic Chemistry; Modified MasteringChemistry with Pearson eText -- ValuePack Access Card; Study Guide and Student Solutions Manual for Organic Chemistry, Books a la Carte Edition (7th Edition)

7th Edition

ISBN: 9780134240152

Author: Paula Yurkanis Bruice

Publisher: PEARSON

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Textbook Question

Chapter 22, Problem 51P

Aspartame (its structure is on page 1007) has a pl of 5.9. Draw its prevailing form at physiological pH (7.4).

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Chapter 22, Problem 50P

Chapter 22, Problem 52P

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Chapter 22 Solutions

Organic Chemistry; Modified MasteringChemistry with Pearson eText -- ValuePack Access Card; Study Guide and Student Solutions Manual for Organic Chemistry, Books a la Carte Edition (7th Edition)

Ch. 22.1 - a. Explain why, when the imidazole ring of...Ch. 22.2 - a. Which isomer(R)-alanine or (S)-alanineis...Ch. 22.2 - Prob. 4P Ch. 22.3 - Prob. 5P Ch. 22.3 - Prob. 6P Ch. 22.3 - Draw the predominant form for glutamate in a...Ch. 22.3 - a. Why is the pKa of the glutamate side chain...Ch. 22.4 - Explain why the pI of lysine is the average of the...Ch. 22.4 - Calculate the pI of each of the following amino...Ch. 22.4 - a. Which amino acid has the lowest pI value? b....

Ch. 22.4 - Prob. 13P Ch. 22.5 - What aldehyde is formed when valine is treated...Ch. 22.5 - Prob. 15P Ch. 22.5 - Prob. 16P Ch. 22.5 - Prob. 17P Ch. 22.5 - Prob. 18P Ch. 22.6 - Why is excess ammonia used in the preceding...Ch. 22.6 - Prob. 20P Ch. 22.6 - What amino acid is formed using the...Ch. 22.6 - Prob. 22P Ch. 22.6 - What amino acid is formed when the aldehyde used...Ch. 22.7 - Esterase is an enzyme that catalyzes the...Ch. 22.8 - Draw the tetrapeptide Ala-Thr-Asp-Asn and indicate...Ch. 22.8 - Prob. 26P Ch. 22.8 - Prob. 27P Ch. 22.8 - Which bonds in the backbone of a peptide can...Ch. 22.9 - What is the configuration about each of the...Ch. 22.9 - Glutathione is a tripeptide whose function is to...Ch. 22.10 - What dipeptides would be formed by heating a...Ch. 22.10 - Suppose you are trying to synthesize the dipeptide...Ch. 22.10 - Show the steps in the synthesis of the...Ch. 22.10 - a. Calculate the overall yield of bradykinin when...Ch. 22.11 - Show the steps in the synthesis of the...Ch. 22.13 - Prob. 36P Ch. 22.13 - In determining the primary structure of insulin,...Ch. 22.13 - A decapeptide undergoes partial hydrolysis to give...Ch. 22.13 - Explain why cyanogen bromide does not cleave on...Ch. 22.13 - Indicate the peptides produced from cleavage by...Ch. 22.13 - Prob. 42P Ch. 22.13 - Three peptides were obtained from a trypsin...Ch. 22.14 - Prob. 44P Ch. 22.15 - How would a protein that resides in the nonpolar...Ch. 22.16 - a. Which would have the greatest percentage of...Ch. 22 - Prob. 47P Ch. 22 - Glycine has pK2 values of 2.34 and 9.60. At what...Ch. 22 - Prob. 49P Ch. 22 - Prob. 50P Ch. 22 - Aspartame (its structure is on page 1007) has a pl...Ch. 22 - Draw the form of aspartate that predominates at...Ch. 22 - A professor was preparing a manuscript for...Ch. 22 - Prob. 54P Ch. 22 - Determine the amino acid sequence of a polypeptide...Ch. 22 - Prob. 56P Ch. 22 - Which is the more effective buffer at...Ch. 22 - Identify the location and type of charge on the...Ch. 22 - Draw the product obtained when a lysine side chain...Ch. 22 - After the polypeptide shown below was treated with...Ch. 22 - Treatment of a polypeptide with 2-mercaptoethanol...Ch. 22 - Show how aspartame can be synthesized using DCCD.Ch. 22 - -Amino acids can be prepared by treating an...Ch. 22 - Reaction of a polypeptide with carboxypeptidase A...Ch. 22 - a. How many different octapeptides can be made...Ch. 22 - Glycine has pKa values of 2.3 and 9.6. Do you...Ch. 22 - A mixture of 15 amino acids gave the fingerprint...Ch. 22 - Write the mechanism for the reaction of an amino...Ch. 22 - Prob. 69P Ch. 22 - Show how valine can be prepared by a. a...Ch. 22 - A chemist wanted to test his hypothesis that the...Ch. 22 - Propose a mechanism for the rearrangement of the...Ch. 22 - A normal polypeptide and a mutant of the...Ch. 22 - Determine the amino acid sequence of a polypeptide...

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Aspartame (its structure is on page 1007) has a pl of 5.9. Draw its prevailing form at physiological pH (7.4).

Solution Summary: The author explains that the prevailing form of aspartame at pH 7.4 was drawn. The isoelectric point is the pH at which the amount of positive and negative charge on an amino

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Chapter 22 Solutions