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Chirality does not give rise to a a pair of stereo-isomers but to a pair of optical isomers.

Optical isomers are identical in every way but one: that the two isomers are mirror images of each other...

they are not superimposeable...

they are defined as + and - or laevo and dextro rotatory (left handed and right handed) because of the effect they have on polarised light. Polarised light is oriented in one plane and passing such light through a laevo rotatory optical isomeric substance it will be rotated through an angle and emerge in a different plane.

In living organisms a higher proportion of one optical isomer over the other occurs.

Substances produced in the lab have more or less equal proportions of each isomer and are called racemic mixtures

A chiral carbon atom is defined as having four differentconstituent atoms or groups of atoms attached to it by means of single covalent chemical bonds.

This confers a status of assymetry to this carbon atom.

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Q: How does the presence of a chiral carbon atom in a molecule give rise to the existence of a pair of stereoisomers?
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