Abstract
I POINTED out some time ago,1 that despite Pasteur's original statement, or at all events, the text-book version of it, optical enantiomers were possibly not completely identical. I followed this up with an investigation of the rotatory powers of the mandelic acids,2 in which at least preliminary evidence of non-identity was obtained. I am about to publish an account of a lengthy investigation of the camphoric acids, in which differences of the same kind have been observed.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callSimilar Papers
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
