ORGANIC CHEMISTRY W/BIOLOGICAL TOPICS
ORGANIC CHEMISTRY W/BIOLOGICAL TOPICS
6th Edition
ISBN: 9781260325294
Author: SMITH
Publisher: RENT MCG
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Chapter 27, Problem 68P
Interpretation Introduction

Interpretation: A stepwise synthesis of the tripeptide Val-Leu-Val from 3methylbutanal[(CH3)2CHCH2CHO] as the only organic starting material is to be devised.

Concept introduction: Amino acids are biologically important organic molecules that contain amine group, carboxyl group and a non polar side chain. Some of the amino acids are glycine, valine, alanine, and many more. Proteins are made up of amino acid units.

When two or more amino acids are linked in a chain, a compound called peptide is formed in which the carboxyl group of each acid is joined to the amino group of the next forming a -OC-NH- bond, known as peptide bond.

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Devise a stepwise synthesis of the tripeptide Val–Leu–Val from 3-methylbutanal [(CH3)2CHCH2CHO] as the only organic starting material. You may also use any required inorganic or organic reagents.
Devise a synthesis of attached compound using CH3CH2CH=CH2 as the starting material. You may use any other organic compounds or inorganic reagents.
Determine the reagents and the structure of the intermediate products to complete the following reaction sequence (1/2 eq.) NaNH, Br OH OH

Chapter 27 Solutions

ORGANIC CHEMISTRY W/BIOLOGICAL TOPICS

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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