Abstract
Several C-nitro compounds were demonstrated to nitrosate morpholine, a secondary amine, to form N-nitrosomorpholine (NMOR). These C-nitro compounds responded to thermal energy analyzer (TEA); however, there was no correlation between the nitrosation rate and the relative TEA molar response of the C-nitro compounds. Alkyl and aromatic C-nitro compounds bearing electron-withdrawing groups such as NO 2, Br, Cl and F were active nitrosating agents. On the other hand, C-nitro compounds without such electron-withdrawing groups did not nitrosate morpholine.
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.
