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ascorbic acid has two optical isomers: L-ascorbic and D-ascorbic acid

In general, there is no difference in the chemical reactivity of the two forms. However if you are using reagents that are stereo-selective, like enzymes, then only one form will be used in the reaction. Usually that would be L-ascorbic acid.
If you have the racemic mixture of the two forms, then you would have 50% of the mixture being L- and 50% D-, so you would have half the concentration/amount of what you would like reacting (for stereoselective reactions with enzymes in vitro or if you are doing experiments with living organisms).

2006-10-10 23:35:45 · answer #1 · answered by bellerophon 6 · 0 0

L-ascorbic acid can rotate polarized light to the left. It is an optically active molecule.

2006-10-10 14:52:57 · answer #2 · answered by cece 1 · 0 0

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