Stereochemistry
From Proteopedia
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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. | 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. | ||
- | <table><tr><td><applet load='' name='A' size='300' frame='true' scene=''/></td><td><applet load='' name='B' size='300' frame='true' scene=''/></td></tr></table> | + | <table><tr><td><applet load='' name='A' size='300' frame='true' scene='82/824489/Rconfig/4'/></td><td><applet load='' name='B' size='300' frame='true' scene='82/824489/Sconfig/4'/></td></tr></table> |
<jmol> | <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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