Assuming that each chirality center is L, the structural formula for each of the given dipeptides is to be shown in a manner that reveals the stereochemistry at the α-carbon atom. Concept Introduction: A peptide bond is an amide bond. A dipeptide contains two amino acids linked by a peptide bond. It is formed between amino group of one amino acid the carboxyl group of the other amino acid. The peptide structures are written, such that the amino group is at the left side and the carboxyl group is at the right side. The left end of the peptide is called the N terminus and the right end is called the C terminus.

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Answer 1

Question

Chapter 26.7, Problem 14P

Interpretation Introduction

Interpretation:

Assuming that each chirality center is L, the structural formula for each of the given dipeptides is to be shown in a manner that reveals the stereochemistry at the α-carbon atom.

Concept Introduction:

A peptide bond is an amide bond. A dipeptide contains two amino acids linked by a peptide bond.

It is formed between amino group of one amino acid the carboxyl group of the other amino acid.

The peptide structures are written, such that the amino group is at the left side and the carboxyl group is at the right side.

The left end of the peptide is called the N terminus and the right end is called the C terminus.

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Answer 2

Question

Chapter 26.7, Problem 14P

Interpretation Introduction

Interpretation:

Assuming that each chirality center is L, the structural formula for each of the given dipeptides is to be shown in a manner that reveals the stereochemistry at the α-carbon atom.

Concept Introduction:

A peptide bond is an amide bond. A dipeptide contains two amino acids linked by a peptide bond.

It is formed between amino group of one amino acid the carboxyl group of the other amino acid.

The peptide structures are written, such that the amino group is at the left side and the carboxyl group is at the right side.

The left end of the peptide is called the N terminus and the right end is called the C terminus.

Expert Solution & Answer

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Answer 3

Question

Chapter 26.7, Problem 14P

Interpretation Introduction

Interpretation:

Assuming that each chirality center is L, the structural formula for each of the given dipeptides is to be shown in a manner that reveals the stereochemistry at the α-carbon atom.

Concept Introduction:

A peptide bond is an amide bond. A dipeptide contains two amino acids linked by a peptide bond.

It is formed between amino group of one amino acid the carboxyl group of the other amino acid.

The peptide structures are written, such that the amino group is at the left side and the carboxyl group is at the right side.

The left end of the peptide is called the N terminus and the right end is called the C terminus.

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Answer 4

Question

Chapter 26.7, Problem 14P

Interpretation Introduction

Interpretation:

Assuming that each chirality center is L, the structural formula for each of the given dipeptides is to be shown in a manner that reveals the stereochemistry at the α-carbon atom.

Concept Introduction:

A peptide bond is an amide bond. A dipeptide contains two amino acids linked by a peptide bond.

It is formed between amino group of one amino acid the carboxyl group of the other amino acid.

The peptide structures are written, such that the amino group is at the left side and the carboxyl group is at the right side.

The left end of the peptide is called the N terminus and the right end is called the C terminus.

Expert Solution & Answer

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Answer 5

Chapter 26.7, Problem 14P

Interpretation Introduction

Interpretation:

Assuming that each chirality center is L, the structural formula for each of the given dipeptides is to be shown in a manner that reveals the stereochemistry at the α-carbon atom.

Concept Introduction:

A peptide bond is an amide bond. A dipeptide contains two amino acids linked by a peptide bond.

It is formed between amino group of one amino acid the carboxyl group of the other amino acid.

The peptide structures are written, such that the amino group is at the left side and the carboxyl group is at the right side.

The left end of the peptide is called the N terminus and the right end is called the C terminus.

Answer 6

Chapter 26.7, Problem 14P

Interpretation Introduction

Interpretation:

Assuming that each chirality center is L, the structural formula for each of the given dipeptides is to be shown in a manner that reveals the stereochemistry at the α-carbon atom.

Concept Introduction:

A peptide bond is an amide bond. A dipeptide contains two amino acids linked by a peptide bond.

It is formed between amino group of one amino acid the carboxyl group of the other amino acid.

The peptide structures are written, such that the amino group is at the left side and the carboxyl group is at the right side.

The left end of the peptide is called the N terminus and the right end is called the C terminus.

Answer 7

Chapter 26.7, Problem 14P

Interpretation Introduction

Interpretation:

Assuming that each chirality center is L, the structural formula for each of the given dipeptides is to be shown in a manner that reveals the stereochemistry at the α-carbon atom.

Concept Introduction:

A peptide bond is an amide bond. A dipeptide contains two amino acids linked by a peptide bond.

It is formed between amino group of one amino acid the carboxyl group of the other amino acid.

The peptide structures are written, such that the amino group is at the left side and the carboxyl group is at the right side.

The left end of the peptide is called the N terminus and the right end is called the C terminus.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 26.1 - Prob. 1P Ch. 26.2 - Prob. 2P Ch. 26.2 - Prob. 3P Ch. 26.3 - Prob. 4P Ch. 26.3 - Prob. 5P Ch. 26.4 - Prob. 6P Ch. 26.4 - Prob. 7P Ch. 26.4 - Prob. 8P Ch. 26.5 - Prob. 9P Ch. 26.6 - Prob. 10P

Solution Summary: The author explains that the structural formula for each of the given dipeptides reveals the stereochemistry at the -carbon atom.

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