A 1:1 mixture of enantiomers is called racemic or a racemate.
A chiral nonracemic compound is a sample of a chiral compound
containing an excess of one enantiomer, either a small excess or an almost
enantiopure sample.
The simplest context in which enantiomers differ is the so-called
optical activity. By this the phenomenon is understood that
a chiral nonracemic compound in solution or as a pure liquid will
influence the plane of linearly polarized light, i.e. rotates that
plane by a certain angle ("optical rotation").
One pure enantiomer rotates clockwise by a certain angle, the other
one counterclockwise by the same angle ("dextrorotatory",
> 0;
"laevorotatory", < 0, the observer is looking against the beam
of light), under well-defined conditions.
A chiral racemic sample does not rotate the plane of polarized
light, it is optically inactive. However, even a chiral nonracemic
compound sample may rotate by an angle too low to be measurable under a
particular set of conditions, so that it is optically inactive as well.
For these reasons we have to differentiate chirality and optical activity.
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