No method like that, other then
You can often crystallize out one enent... by using a known enemtiomer...
I believe some people use OTC tartaric acid to get the D-meth from the racemic... Pretty sure the OTC tartaric acid is the D...
you should have read in the link I posted to you:
I highly doubt you'd have the L, or the recemic, but possibly the recemic if it is synthetic.. You can determine if it is racemic vs just an enentiomer via a polarmeter I'd think...
You can often crystallize out one enent... by using a known enemtiomer...
I believe some people use OTC tartaric acid to get the D-meth from the racemic... Pretty sure the OTC tartaric acid is the D...
you should have read in the link I posted to you:
Quote
Enantiomers have, when present in a symmetric environment, identical chemical and physical properties except for their ability to rotate plane-polarized light (+/-) by equal amounts but in opposite directions. A mixture of equal parts of an optically active isomer and its enantiomer is termed racemic and has a net rotation of plane-polarized light of zero.
I highly doubt you'd have the L, or the recemic, but possibly the recemic if it is synthetic.. You can determine if it is racemic vs just an enentiomer via a polarmeter I'd think...