Chirality

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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.










 
 
  (c) Lehrstuhl für Mathematik II Universität Bayreuth