From the mechanistic standpoint alkaline hydrolysis of substituted benzoates has repeatedly been studied carefully and much rate data in various conditions are now available (l-3). Nowever, all these measurements were carried out in organic solvents containing relatively small amounts of water.
β¦ LIBER β¦
The alkaline hydrolysis of substituted ethyl benzoates. The additive effects of substituents
β Scribed by Jones, Brynmor ;Robinson, John
- Book ID
- 111888772
- Publisher
- The Royal Society of Chemistry
- Year
- 1955
- Weight
- 576 KB
- Category
- Article
- ISSN
- 0368-1769
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Ortho effects III. Rates of alkaline hyd
β
Masaru Hojo; Masamori Utaka; Zen-ichi Xoshida
π
Article
π
1966
π
Elsevier Science
π
French
β 206 KB
Ortho effects IV. Rates of alkaline hydr
β
Masaru Hojo; Masanori Utaka; Zen-ichi Yoshida
π
Article
π
1966
π
Elsevier Science
π
French
β 235 KB
In our last pa&u (I) it ras reported that in the olkaline'hydrolysis of substituted ethyl bensoates the change of the solvent from' 85 %(rt.) aqueous ethanol to 3 %(rt.) aqueous ethanol caused 5C times increase in the rate of the unsubstituted compound and decrease to a half in the Bammett p value,
Kinetics of the alkaline hydrolysis of e
β
Bell, R. P.; Coller, B. A. W.
π
Article
π
1965
π
Royal Society of Chemistry
β 665 KB
Kinetic Study of Hydrolysis of Benzoates
β
Nummert, Vilve; Piirsalu, Mare; MΓ€emets, Vahur; Koppel, Ilmar
π
Article
π
2006
π
UOCHB
π
English
β 154 KB
286. The kinetics of alkaline hydrolysis
β
Fischer, A. ;Mitchell, W. J. ;Ogilvie, G. S. ;Packer, J. ;Packer, J. E. ;Vaughan
π
Article
π
1958
π
The Royal Society of Chemistry
β 445 KB
Absence of carbonyl oxygen exchange conc
β
Shain, Sydney A.; Kirsch, Jack F.
π
Article
π
1968
π
American Chemical Society
π
English
β 963 KB