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Crystallization of a racemate can result in separate ( ) and (−) forms, or a single racemic compound.In general, most biochemical reactions are stereoselective, so only one stereoisomer will produce the intended product while the other simply does not participate or can cause side-effects.Because of the distortions and lies spread by fundamentalists about scientific dating there is a need for a centralized source of information on the topic.

Apparently a result of the shadow cast by one of the girl's legs onto the other, the picture also appears to show a penis between her legs.The two forms, which are non-superimposable when rotated in 3-dimensional space, are said to be enantiomers.The notation is not to be confused with -glyceraldehyde.Racemate may have different physical properties from either of the pure enantiomers because of the differential intermolecular interactions (see Biological Significance section).The change from a pure enantiomer to a racemate can change its density, melting point, solubility, heat of fusion, refractive index, and its various spectra.

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The production and analysis of enantiomers in the pharmaceutical industry is studied in the field of chiral organic synthesis.

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