The most important reaction of amino acid is formation of peptide bonds. In this reaction amines and acid can condense gives water and form amides. The amide linkage between the amino acids is called a peptide bond. In this way, any number of amino acid can be bonded in a continuous chain. Or Concept Introduction: Any number of amino acids can be bonded in a continuous chain in any order. The end of the peptide with the free amino group ( − NH 3 + ) is called N − terminus and the end of the peptide with the free carboxyl group It is called C -terminus. Peptide structures are generally drawn with N − terminus at the left and C terminus at the right. The nomenclature of peptide is also in the same sequence. Ex:

Question

Want to see the full answer?

Answer 1

Question

Chapter 16.3, Problem 16.19QAP

Interpretation Introduction

Interpretation:

The most important reaction of amino acid is formation of peptide bonds. In this reaction amines and acid can condense gives water and form amides. The amide linkage between the amino acids is called a peptide bond. In this way, any number of amino acid can be bonded in a continuous chain.

Or

Concept Introduction:

Any number of amino acids can be bonded in a continuous chain in any order. The end of the peptide with the free amino group $(- {NH}_{3}^{+})$ is called $N -$ terminus and the end of the peptide with the free carboxyl group

It is called $C$ -terminus. Peptide structures are generally drawn with $N -$ terminus at the left and $C$ terminus at the right. The nomenclature of peptide is also in the same sequence.

Ex:

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 2

Question

Chapter 16.3, Problem 16.19QAP

Interpretation Introduction

Interpretation:

The most important reaction of amino acid is formation of peptide bonds. In this reaction amines and acid can condense gives water and form amides. The amide linkage between the amino acids is called a peptide bond. In this way, any number of amino acid can be bonded in a continuous chain.

Or

Concept Introduction:

Any number of amino acids can be bonded in a continuous chain in any order. The end of the peptide with the free amino group $(- {NH}_{3}^{+})$ is called $N -$ terminus and the end of the peptide with the free carboxyl group

It is called $C$ -terminus. Peptide structures are generally drawn with $N -$ terminus at the left and $C$ terminus at the right. The nomenclature of peptide is also in the same sequence.

Ex:

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 16.3, Problem 16.19QAP

Interpretation Introduction

Interpretation:

The most important reaction of amino acid is formation of peptide bonds. In this reaction amines and acid can condense gives water and form amides. The amide linkage between the amino acids is called a peptide bond. In this way, any number of amino acid can be bonded in a continuous chain.

Or

Concept Introduction:

Any number of amino acids can be bonded in a continuous chain in any order. The end of the peptide with the free amino group $(- {NH}_{3}^{+})$ is called $N -$ terminus and the end of the peptide with the free carboxyl group

It is called $C$ -terminus. Peptide structures are generally drawn with $N -$ terminus at the left and $C$ terminus at the right. The nomenclature of peptide is also in the same sequence.

Ex:

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 16.3, Problem 16.19QAP

Interpretation Introduction

Interpretation:

The most important reaction of amino acid is formation of peptide bonds. In this reaction amines and acid can condense gives water and form amides. The amide linkage between the amino acids is called a peptide bond. In this way, any number of amino acid can be bonded in a continuous chain.

Or

Concept Introduction:

Any number of amino acids can be bonded in a continuous chain in any order. The end of the peptide with the free amino group $(- {NH}_{3}^{+})$ is called $N -$ terminus and the end of the peptide with the free carboxyl group

It is called $C$ -terminus. Peptide structures are generally drawn with $N -$ terminus at the left and $C$ terminus at the right. The nomenclature of peptide is also in the same sequence.

Ex:

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 16.3, Problem 16.19QAP

Interpretation Introduction

Interpretation:

The most important reaction of amino acid is formation of peptide bonds. In this reaction amines and acid can condense gives water and form amides. The amide linkage between the amino acids is called a peptide bond. In this way, any number of amino acid can be bonded in a continuous chain.

Or

Concept Introduction:

Any number of amino acids can be bonded in a continuous chain in any order. The end of the peptide with the free amino group $(- {NH}_{3}^{+})$ is called $N -$ terminus and the end of the peptide with the free carboxyl group

It is called $C$ -terminus. Peptide structures are generally drawn with $N -$ terminus at the left and $C$ terminus at the right. The nomenclature of peptide is also in the same sequence.

Ex:

Answer 6

Chapter 16.3, Problem 16.19QAP

Interpretation Introduction

Interpretation:

The most important reaction of amino acid is formation of peptide bonds. In this reaction amines and acid can condense gives water and form amides. The amide linkage between the amino acids is called a peptide bond. In this way, any number of amino acid can be bonded in a continuous chain.

Or

Concept Introduction:

Any number of amino acids can be bonded in a continuous chain in any order. The end of the peptide with the free amino group $(- {NH}_{3}^{+})$ is called $N -$ terminus and the end of the peptide with the free carboxyl group

It is called $C$ -terminus. Peptide structures are generally drawn with $N -$ terminus at the left and $C$ terminus at the right. The nomenclature of peptide is also in the same sequence.

Ex:

Answer 7

Chapter 16.3, Problem 16.19QAP

Interpretation Introduction

Interpretation:

The most important reaction of amino acid is formation of peptide bonds. In this reaction amines and acid can condense gives water and form amides. The amide linkage between the amino acids is called a peptide bond. In this way, any number of amino acid can be bonded in a continuous chain.

Or

Concept Introduction:

Any number of amino acids can be bonded in a continuous chain in any order. The end of the peptide with the free amino group $(- {NH}_{3}^{+})$ is called $N -$ terminus and the end of the peptide with the free carboxyl group

It is called $C$ -terminus. Peptide structures are generally drawn with $N -$ terminus at the left and $C$ terminus at the right. The nomenclature of peptide is also in the same sequence.

Ex:

Answer 8

Expert Solution & Answer

Answer 9

Expert Solution & Answer

Answer 10

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 11

Ch. 16.1 - Classify each of the following proteins according...Ch. 16.1 - Prob. 16.2QAP Ch. 16.1 - Prob. 16.3QAP Ch. 16.1 - Prob. 16.4QAP Ch. 16.1 - Draw the structure for each of the following amino...Ch. 16.1 - Draw the structure for each of the following amino...Ch. 16.1 - Draw the strcture for each of the following amino...Ch. 16.1 - Prob. 16.8QAP Ch. 16.1 - Prob. 16.9QAP Ch. 16.1 - Prob. 16.10QAP

Want to see the full answer?

Chapter 16 Solutions