The enantiomeric excess of an enantiomer pair is the magnitude of the difference between their relative mole fractions, , often reported as a percentage. Here counts the pair only, excluding solvent; the signs label optical rotation under the specified conditions, not R and S configuration.
In the model above, and give . Keep the same total pair concentration , path length, solvent, temperature and wavelength. The two contributions areThe pure-member reference therefore gives . This ratio measures signed population imbalance only for a pure pair with additive linear responses under matching conditions. Adding unrelated solutes, changing total concentration, or changing chemical equilibrium can invalidate that inference. For , the racemate gives zero net optical rotation by cancellation; each molecule remains chiral. A zero reading alone proves neither a racemate nor molecular achirality.
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Enantiomeric excess (ee) is a measure of the purity of a chiral compound in terms of the proportion of one enantiomer relative to the other. Enantiomers are pairs of molecules that are non-superimposable mirror images of each other, and they often differ in their biological activity and properties.