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Stereochemistry
From Proteopedia
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<jmol> | <jmol> | ||
| - | <jmolButton> | ||
| - | <target>A</target> | ||
| - | <script>script /scripts/82/824489/Rconfig/4.spt; script applet B @{"script /scripts/82/824489/Sconfig/4.spt"};</script> | ||
| - | <text>2-Butanol</text> | ||
| - | </jmolButton></jmol> <jmol> | ||
<jmolButton> | <jmolButton> | ||
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<script>load $erythrose; script applet B @{"load $threose"};</script> | <script>load $erythrose; script applet B @{"load $threose"};</script> | ||
<text>Erythrose vs. Threose</text> | <text>Erythrose vs. Threose</text> | ||
| + | </jmolButton></jmol> <jmol> | ||
| + | <jmolButton> | ||
| + | <target>A</target> | ||
| + | <script>script /scripts/82/824489/Rconfig/4.spt; script applet B @{"script /scripts/82/824489/Sconfig/4.spt"};</script> | ||
| + | <text>reload initial scenes</text> | ||
</jmolButton></jmol> | </jmolButton></jmol> | ||
Revision as of 15:28, 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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