ORGANIC CHEMISTRY
ORGANIC CHEMISTRY
6th Edition
ISBN: 9781266633973
Author: SMITH
Publisher: MCG
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Chapter 27, Problem 56P
Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of angiotensin I with trypsin are to be predicted.

Concept introduction: The name of amino acids is represented by the one-letter and three-letter abbreviations. There are some enzymes used to hydrolyzed the specific sites of peptides. The carboxypeptidase enzymes are used to identify the C-terminal amino acid.

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of angiotensin I with chymotrypsin are to be predicted.

Concept introduction: The name of amino acids is represented by the one-letter and three-letter abbreviations. There are some enzymes are used to hydrolyzed the specific sites of peptides. The carboxypeptidase enzymes are used to identify the C-terminal amino acid.

Interpretation Introduction

(c)

Interpretation: The sequence of the amino acid in angiotensin II using three-letter abbreviations is to be given.

Concept introduction: The name of amino acids is represented by the one-letter and three-letter abbreviations. There are some enzymes are used to hydrolyzed the specific sites of peptides. The carboxypeptidase enzymes are used to identify the C-terminal amino acid.

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Chapter 27 Solutions

ORGANIC CHEMISTRY

Ch. 27.3 - Prob. 11PCh. 27.3 - Prob. 12PCh. 27.4 - Problem 29.13 What alkene is needed to synthesize...Ch. 27.5 - Problem 29.14 Draw the structure of each peptide....Ch. 27.5 - Problem 29.15 Name each peptide using both the...Ch. 27 - Draw the product formed when the following amino...Ch. 27 - With reference to the following peptide: a...Ch. 27 - Prob. 31PCh. 27 - Histidine is classified as a basic amino acid...Ch. 27 - Tryptophan is not classified as a basic amino acid...Ch. 27 - What is the structure of each amino acid at its...Ch. 27 - What is the predominant form of each of the...Ch. 27 - 29.37 What is the predominant form of each of the...Ch. 27 - a. Draw the structure of the tripeptide A–A–A, and...Ch. 27 - 29.39 Draw the organic products formed in each...Ch. 27 - 29.40 What alkyl halide is needed to synthesize...Ch. 27 - Prob. 50PCh. 27 - Draw the structure for each peptide: (a) Phe–Ala;...Ch. 27 - 29.52 For the tetrapeptide Asp–Arg–Val–Tyr: a....Ch. 27 - Prob. 53PCh. 27 - Prob. 54PCh. 27 - 29.55 Draw the amino acids and peptide fragments...Ch. 27 - Prob. 56PCh. 27 - Prob. 57PCh. 27 - Prob. 58PCh. 27 - 29.59 An octapeptide contains the following amino...Ch. 27 - 29.60 Draw the organic products formed in each...Ch. 27 - 29.65 Draw the mechanism for the reaction that...Ch. 27 - 29.66 Which of the following amino acids are...Ch. 27 - 29.67 After the peptide chain of collagen has been...Ch. 27 - Prob. 68PCh. 27 - Prob. 69PCh. 27 - 29.70 The anti-obesity drug orlistat works by...Ch. 27 - Prob. 71P
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