Stereochemistry: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
Line 4: | Line 4: | ||
<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> | ||
<target>A</target> | <target>A</target> |
Revision as of 18:27, 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.
|
|