Stereochemistry
From Proteopedia
(Difference between revisions)
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<script>script /scripts/85/859020/Cis-butene/1.spt; script applet B @{"load $butanol"};</script> | <script>script /scripts/85/859020/Cis-butene/1.spt; script applet B @{"load $butanol"};</script> | ||
<text>2-Butanol</text> | <text>2-Butanol</text> | ||
- | </jmolButton></jmol> | + | </jmolButton></jmol><jmol> |
- | <jmol> | ||
<jmolButton> | <jmolButton> | ||
<target>A</target> | <target>A</target> | ||
- | <script>load "$ | + | <script>load "$2-butene"; script applet B @{"load $butene"};</script> |
<text>Butene</text> | <text>Butene</text> | ||
- | </jmolButton></jmol> | + | </jmolButton></jmol><jmol> |
- | <jmol> | ||
<jmolButton> | <jmolButton> | ||
<target>A</target> | <target>A</target> | ||
<script>load "$D-alanine"; script applet B @{"load $alanine"};</script> | <script>load "$D-alanine"; script applet B @{"load $alanine"};</script> | ||
<text>Alanine enantiomers</text> | <text>Alanine enantiomers</text> | ||
- | </jmolButton></jmol> | + | </jmolButton></jmol><jmol> |
- | |||
- | <jmol> | ||
<jmolButton> | <jmolButton> | ||
<target>A</target> | <target>A</target> |
Revision as of 15:16, 14 August 2020
Stereochemistry refers to the three dimensional arrangement of atoms in molecules, especially those aspects that go beyond the connectivity (which atoms are connected to each other) captured in a Lewis structure. Two molecules that are mirror images of each other (enantiomers) differ in stereochemistry. Another common example are cis and trans double bonds, such as in fatty acids.
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