Abstract
The two adducts obtained from the Diels-Alder condensation between 1,3-cyclohexadiene and trans-p-Chloro-β-nitrostyrene have been characterized from the PMR spectra of the respective cyclohexane dicarboxylic acids obtained from chromic acid oxidation of the adducts. The Diels-Alder condensation yielded a larger quantity of the isomer with the nitro group endo to the double bond. Hydrogenation of the double bond in the two adducts yielded one product, the PMR spectrum of which is consistent with the expected product. The PMR spectra of the adducts, their oxidation products and the hydrogenation product are reported and discussed.
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 callDisclaimer: 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.
