The Lewis structure for the tripeptide tyrosine-histidine-glycine has to be drawn. Concept introduction: Amino acids condense to form peptide bonds releasing small water molecules. A peptide bond is the chemical bond which is formed between two molecules of amino acid when carboxyl group of one molecule reacts with the amino group of another molecule. A polypeptide containing n amino acids will have ( n − 1 ) peptide bonds. The side of a polypeptide chain having free carboxylic group is called C-terminal and the side having free amino group is called N-terminal end.

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Answer 1

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Chapter 24, Problem 8PS

Interpretation Introduction

Interpretation:

The Lewis structure for the tripeptide tyrosine-histidine-glycine has to be drawn.

Concept introduction: Amino acids condense to form peptide bonds releasing small water molecules. A peptide bond is the chemical bond which is formed between two molecules of amino acid when carboxyl group of one molecule reacts with the amino group of another molecule. A polypeptide containing n amino acids will have (n−1) peptide bonds.

The side of a polypeptide chain having free carboxylic group is called C-terminal and the side having free amino group is called N-terminal end.

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Answer 2

Question

Chapter 24, Problem 8PS

Interpretation Introduction

Interpretation:

The Lewis structure for the tripeptide tyrosine-histidine-glycine has to be drawn.

Concept introduction: Amino acids condense to form peptide bonds releasing small water molecules. A peptide bond is the chemical bond which is formed between two molecules of amino acid when carboxyl group of one molecule reacts with the amino group of another molecule. A polypeptide containing n amino acids will have (n−1) peptide bonds.

The side of a polypeptide chain having free carboxylic group is called C-terminal and the side having free amino group is called N-terminal end.

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Answer 3

Question

Chapter 24, Problem 8PS

Interpretation Introduction

Interpretation:

The Lewis structure for the tripeptide tyrosine-histidine-glycine has to be drawn.

Concept introduction: Amino acids condense to form peptide bonds releasing small water molecules. A peptide bond is the chemical bond which is formed between two molecules of amino acid when carboxyl group of one molecule reacts with the amino group of another molecule. A polypeptide containing n amino acids will have (n−1) peptide bonds.

The side of a polypeptide chain having free carboxylic group is called C-terminal and the side having free amino group is called N-terminal end.

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Answer 4

Question

Chapter 24, Problem 8PS

Interpretation Introduction

Interpretation:

The Lewis structure for the tripeptide tyrosine-histidine-glycine has to be drawn.

Concept introduction: Amino acids condense to form peptide bonds releasing small water molecules. A peptide bond is the chemical bond which is formed between two molecules of amino acid when carboxyl group of one molecule reacts with the amino group of another molecule. A polypeptide containing n amino acids will have (n−1) peptide bonds.

The side of a polypeptide chain having free carboxylic group is called C-terminal and the side having free amino group is called N-terminal end.

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Answer 5

Chapter 24, Problem 8PS

Interpretation Introduction

Interpretation:

The Lewis structure for the tripeptide tyrosine-histidine-glycine has to be drawn.

Concept introduction: Amino acids condense to form peptide bonds releasing small water molecules. A peptide bond is the chemical bond which is formed between two molecules of amino acid when carboxyl group of one molecule reacts with the amino group of another molecule. A polypeptide containing n amino acids will have (n−1) peptide bonds.

The side of a polypeptide chain having free carboxylic group is called C-terminal and the side having free amino group is called N-terminal end.

Answer 6

Chapter 24, Problem 8PS

Interpretation Introduction

Interpretation:

The Lewis structure for the tripeptide tyrosine-histidine-glycine has to be drawn.

Concept introduction: Amino acids condense to form peptide bonds releasing small water molecules. A peptide bond is the chemical bond which is formed between two molecules of amino acid when carboxyl group of one molecule reacts with the amino group of another molecule. A polypeptide containing n amino acids will have (n−1) peptide bonds.

The side of a polypeptide chain having free carboxylic group is called C-terminal and the side having free amino group is called N-terminal end.

Answer 7

Chapter 24, Problem 8PS

Interpretation Introduction

Interpretation:

The Lewis structure for the tripeptide tyrosine-histidine-glycine has to be drawn.

Concept introduction: Amino acids condense to form peptide bonds releasing small water molecules. A peptide bond is the chemical bond which is formed between two molecules of amino acid when carboxyl group of one molecule reacts with the amino group of another molecule. A polypeptide containing n amino acids will have (n−1) peptide bonds.

The side of a polypeptide chain having free carboxylic group is called C-terminal and the side having free amino group is called N-terminal end.

Answer 8

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Answer 11

Ch. 24.1 - Draw the Lewis structure for the tripeptide...Ch. 24.3 - What is the sequence of the strand of DNA...Ch. 24.3 - Prob. 24.3CYU Ch. 24.5 - Kynamro has the hydrogen bonding sequence:...Ch. 24.5 - The formula of Kynamro is...Ch. 24.5 - Prob. 1.3ACP Ch. 24.5 - Prob. 2.1ACP Ch. 24.5 - Prob. 2.2ACP Ch. 24.5 - Prob. 2.3ACP Ch. 24 - (a) Draw the Lewis structure for the amino acid...

Solution Summary: The author explains the Lewis structure for the tripeptide tyrosine-histidine-glycine.

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