Chapter 4: Q79 P (page 183)
Are the following pairs identical, enantiomers, diastereomers, or constitutional isomers?
Short Answer
- They are diastereomers.
- They are enantiomers.
- They are Constitutional isomers.
- They are identical.
/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none}
Learning Materials
Features
Discover
Chapter 4: Q79 P (page 183)
Are the following pairs identical, enantiomers, diastereomers, or constitutional isomers?
All the tools & learning materials you need for study success - in one app.
Get started for free
The following compound has only one asymmetric centre. Why then does it have four stereoisomers?
Which of the following compounds has an asymmetric center?

Naproxen, a nonsteroidal anti-inflammatory drug that is the active ingredient in Aleve (p. 115), has a specific rotation of +66. One commercial preparation result in a mixture with a 97% enantiomeric excess.
a. Does naproxen have the R or the S configuration?
b. What percent of each enantiomer is obtained from the commercial preparation?
(S)- (+)-Monosodium glutamate (MSG) is a flavour enhancer used in many foods. Some people have an allergic reaction to MSG (including headache, chest pains, and an overall feeling of weakness). Fast food often contains substantial amounts of MSG, which is widely used in Chinese food as well. (S)-(+)-MSG has a specific rotation of +24.

a. What is the specific rotation of (R)- (-)-monosodium glutamate?
b. What is the specific rotation of a racemic mixture of MSG?
Question: Name the following compounds using R,S designations:

What do you think about this solution?
We value your feedback to improve our textbook solutions.