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File:Mecoprop-racemic-dimer-from-xtal-3D-balls.png

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Ball-and-stick model of an enantiomeric pair of mecoprop molecules, as found in the crystal structure of racemic mecoprop. The (S)-(−)-enantiomer is on the left; the (R)-(+) enantiomer is to the right.

X-ray crystallographic data from G. Smith, C. H. L. Kennard, A. H. White and P. G. Hodgson (April 1980). "(+-)-2-(4-Chloro-2-methylphenoxy)propionic acid (mecoprop)". Acta Cryst. B36 (4): 992-994. DOI:10.1107/S0567740880005134..

Model constructed in CrystalMaker 8.1.

Image generated in Accelrys DS Visualizer.
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Author Ben Mills
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current17:11, 25 January 2009Thumbnail for version as of 17:11, 25 January 20091,100 × 696 (160 KB)Benjah-bmm27 (talk | contribs){{Information |Description = Ball-and-stick model of an enantiomeric pair of mecoprop molecules, as found in the crystal structure of racemic mecoprop. The (''S'')-(−)-enantiomer is on the left; the (''R'')-(+) enantiomer is to the right. X-ray crystal

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