
%0 Journal Article
%A Harvey, GJ 
%A Stimson, VR 
%T Kinetics of Alkyl-oxygen Fission in Ester Hydrolysis: Tertiary Amyl and &#945;-Methylallyl Esters
%J Australian Journal of Chemistry
%D 1962/12/01
%V 15
%N 4
%P 757-763
%K 
%R https://doi.org/10.1071/CH9620757
%U https://www.publish.csiro.au/paper/CH9620757 
%X The rates and Arrhenius parameters for the acid-catalysed hydrolyses of tertiary amyl 2,4,6-trimethylbenzoate and benzoate and &#945;-methylallyl 2,4,6-trimethylbenzoate, benzoate, and acetate in aqueous acetone imply that reaction occurs by mechanism AALl for the former group and that a transition from mechanism AALl to AAC2 occurs between the benzoate and acetate in the latter series. 
