ORGANIC CHEMISTRY-ETEXT REG ACCESS
ORGANIC CHEMISTRY-ETEXT REG ACCESS
12th Edition
ISBN: 9781119308362
Author: Solomons
Publisher: WILEY
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Chapter 5, Problem 5PP
Interpretation Introduction

Interpretation:

The chiral centers of limonene and thalidomide are to be shown.

Concept introduction:

Chirality centers are the atoms (usually carbons) with four different substituents.

A chirality center creates a non-superimposable mirror image.

An atom having four unidentical substituents will be a chirality center.

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Coibacin B (shown below) is a natural product that exhibits potent anti-inflammatory activity and potential activity in the treatment of leishmaniasis, a disease caused by certain parasites (Org. Lett. 2012, 14, 3878-3881): (a) Assign the configuration (R or S) of each chirality center (labeled A to C) in coibacin B. (b) Identify the number of possible stereoisomers for this compound, assuming that the geometry of the alkenes are fixed. Choices are given below and write the CAPITAL LETTER of your choice. A. 2 В. 4 С. 8 D. 16 ANSWERS: (a) A. В. C. (b)
5:51 Draw examples of the following: (a) A meso compound with the formula C8H18 (b) A meso compound with the formula C9H20 (c) A compound with two chirality centers, one R and the other S
(a) Which compounds (B–F) are identical to A? (b) Which compounds (B–F) represent an isomer of A?

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ORGANIC CHEMISTRY-ETEXT REG ACCESS

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