Stereochemistry: Difference between revisions

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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>
Line 32: Line 27:
     <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 18:28, 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.

Drag the structure with the mouse to rotate
Drag the structure with the mouse to rotate

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Karsten Theis