EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
6th Edition
ISBN: 8220103151757
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 6, Problem 6.17P
Interpretation Introduction

(a)

Interpretation:

The effect on the given enantiomeric resolution by the given condition is to be stated.

Concept introduction:

A carbon atom that has four nonequivalent atoms or groups attached to it is known as the chiral carbon atom. Chiral carbon centers are also called as asymmetric or stereogenic centers. The chiral atom sometimes results in the formation of enantiomers which are the non-superimposable mirror images of each other.

Interpretation Introduction

(b)

Interpretation:

The effect on the given enantiomeric resolution by the given condition is to be stated.

Concept introduction:

A carbon atom that has four nonequivalent atoms or groups attached to it is known as the chiral carbon atom. Chiral carbon centers are also called as asymmetric or stereogenic centers. The chiral atom sometimes results in the formation of enantiomers which are the non-superimposable mirror images of each other.

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Calculate the enantiomeric excess for the sample of (S)- ibuprofen sample and (R)-ibuprofen sample based on the data in attached image?
(a) Draw all other stereoisomers of the molecule , labelling meso forms (if any), and assign descriptors to chiral carbon atoms.   (b) Including molecule below, label pairs of enantiomers and pairs of diastereomers.   (c) If you were to distill a mixture of all the isomers, how many fractions could be obtained, and what is in each fraction?
(c) What is the optical purity of a sample of the (S)-enantiomer if one- third of it under went conversion to its mirror image?
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