ORGANIC CHEMISTRY
ORGANIC CHEMISTRY
9th Edition
ISBN: 9780134645704
Author: WADE AND SIMEK
Publisher: PEARSON
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Chapter 25.5, Problem 25.8P
Interpretation Introduction

Interpretation: An explanation to show that the phosphatidic acid is chiral, even though none of its fatty acids are chiral is to be stated and identification of asymmetric carbon in phosphatidic acid is to be done.

Concept introduction: A carbon atom, linked to four different functional groups in a compound is known as an asymmetric carbon. An asymmetric carbon is also known as chiral carbon.

To determine: An explanation to show that the phosphatidic acid is chiral, even though none of its fatty acids are chiral and identification of asymmetric carbon in phosphatidic acid.

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Q1: Draw the most stable and the least stable Newman projections about the C2-C3 bond for each of the following isomers (A-C). Are the barriers to rotation identical for enantiomers A and B? How about the diastereomers (A versus C or B versus C)? enantiomers H Br H Br (S) CH3 H3C (S) (R) CH3 H3C H Br A Br H C H Br H3C (R) B (R)CH3 H Br H Br H3C (R) (S) CH3 Br H D identical
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