Abstract
1. The kinetics of the alkaline hydrolysis of substituted phenyl thionophosphinates and acetates has been studied. The activation parameters were calculated, and their dependence on the structure of the leaving group of the esters and the composition of the medium has been analyzed. 2. Polylinear regression dependences were obtained, which show the influence of all the experimentally controlled factors on the hydrolysis of esters (I) and (II). It was concluded that the detailed mechanisms of the alkaline hydrolysis of thionophosphinates and acetates in mixtures of water with acetonitrile are similar.
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 callMore From: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
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.
