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It is shown via a series of numerical tests on the camphor molecule, C10H16O, that the naturally occurring d-enantiomer is energetically stabilized with respect to its mirror image by electroweak force. The calculated energy difference between enantiomers, about 1.5 x 10(-19) hartree, is roughly eight orders of magnitude smaller than the upper bound suggested by available spectroscopic investigations on the frequency of a spectroscopic transition. However, such a difference is about ten times larger than previous estimates of parity-violating energy contributions reported in the literature for other chiral molecules, which makes the idea of electroweak stabilization of one enantiomer more reliable than expected before.
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Lazzeretti et al. (1999) studied this question.
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