Abstract
The composition of the products of photolysis of acetone in the presence of methyl chloride, methyl bromide, methylene chloride, and methylene bromide has been determined. These reactions are attended by complications not found with the photolysis of acetone–hydrocarbon mixtures. Failure to take into account reactions resulting from the formation of halogen hydrides and to allow for the presence of ethylene invalidates the values obtained by Raal and Steacie for the activation energy for hydrogen abstraction by methyl radicals from some halogenated hydrocarbons.
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.
