Abstract
Using a new semirigid model, conformation maps of cyclohexane, p‐dioxane, m‐dioxane, and cycloheptane are recalculated. The ideal out‐of‐plane coordinates are used together with in‐plane coordinates and are found to give the correct energies of all the significant conformations of six membered rings and of the chair–twist–chair form of cycloheptane. Conformation maps display higher symmetry than maps previously reported.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.