"Dishing Out" Stereochemical Principles

Harold Hart
Department of Chemistry, Michigan State University, East Lansing, MI 48824-1322
J. Chem. Educ., 2001, 78 (12), p 1632
DOI: 10.1021/ed078p1632
Publication Date (Web): December 1, 2001

Abstract

Otherwise identical plates with suitable stick-on labels near the edges are used as models to illustrate the principles of stereochemistry. Symmetry axes, enantiomers, meso forms, diastereomers, and molecules with multiple stereogenic centers are readily visualized.

Keywords (Audience):

First-Year Undergraduate / General

Keywords (Domain):

Demonstrations

Keywords (Pedagogy):

Analogies / Transfer

Keywords (Subject):

Chirality / Optical Activity

Citing Articles

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This article has been cited by 5 ACS Journal articles (5 most recent appear below).

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      Several pedagogical objects can be used to discuss chirality. Here, we use the cut of an apple to show that the association of identical chiral moieties can form a non-chiral object. Octahedral chirality is used to find situations equivalent to the cut of ...

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    Chirality Made Simple: A 1- and 2-Dimensional Introduction to Stereochemistry

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      Using internal and external reflection elements in one-, two-, and three-dimensional space, the concept of chirality can be introduced in simple terms that are readily understood. Illustrations of 2-D chirality include block letters of the alphabet and ...

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    Demonstration of Enantiomer Specificity of Proteins and Drugs

    Gretchen L. Anderson , Shallee T. Page
    Journal of Chemical Education2004 81 (7), 971
    • Demonstration of Enantiomer Specificity of Proteins and Drugs

      Gretchen L. Anderson , Shallee T. Page
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      In addition to the traditional use of molecular models of tetrahedral asymmetric centers, the concept of chirality and its importance to protein–drug interactions is demonstrated in a guided classroom activity. A watchglass with three different colored ...

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History

  • Received: August 03, 2009

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