Only three distinct stereoisomers of 1,3-dimethylcyclohexane are possible. These include a pair of enantiomers (bottom) and a single achiral stereoisomer.

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The nomogram is also not useful if the time of ingestion is uncertain, if ingestion occurred more than 24 hours before presentation, or if repeated ingestion.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Meso Compounds Section 5.6.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Presentation transcript:

Only three distinct stereoisomers of 1,3-dimethylcyclohexane are possible. These include a pair of enantiomers (bottom) and a single achiral stereoisomer (top) that is diastereomeric with each of the chiral stereoisomers. Source: Stereochemistry, The Organic Chemistry of Medicinal Agents Citation: Renslo A. The Organic Chemistry of Medicinal Agents; 2016 Available at: http://accesspharmacy.mhmedical.com/DownloadImage.aspx?image=/data/books/1731/renslo_ch03_fig-03-06.png&sec=116669156&BookID=1731&ChapterSecID=116669137&imagename= Accessed: November 14, 2017 Copyright © 2017 McGraw-Hill Education. All rights reserved

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