Quarterly Journal of the Chemical Society of London, Volume 6 |
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Results 1-3 of 88
Page 1076
... reduction of 1 - chloronitroethane by the radicals CMe , OH , CMe2OCHMe2 , and ⚫CO2H at pH 1.8 Reducing agent aN ( 1 ) ан ( 1 ) acı ( 1 ) • CH2OH • 24.9 1.3 4.1 • CHMe OH a , b 24.1 1.4 4.1 • CHMe⚫OEt 24.4 1.3 3.8 • C , H , O C • CH ...
... reduction of 1 - chloronitroethane by the radicals CMe , OH , CMe2OCHMe2 , and ⚫CO2H at pH 1.8 Reducing agent aN ( 1 ) ан ( 1 ) acı ( 1 ) • CH2OH • 24.9 1.3 4.1 • CHMe OH a , b 24.1 1.4 4.1 • CHMe⚫OEt 24.4 1.3 3.8 • C , H , O C • CH ...
Page 1136
... reduction of benzophenones is more complex and that the hydrogen atoms of the first - formed alkoxy - derivatives are not available for reduction . This was a reason for again limiting our observations to the first 30 % of reaction ...
... reduction of benzophenones is more complex and that the hydrogen atoms of the first - formed alkoxy - derivatives are not available for reduction . This was a reason for again limiting our observations to the first 30 % of reaction ...
Page 1239
... Reduction of Isatogens By J. E. Bunney and M. Hooper , School of Pharmacy , Sunderland Polytechnic , Sunderland , Co. Durham The polarographic reduction of a number of isatogens has been studied . The results show that the reduction ...
... Reduction of Isatogens By J. E. Bunney and M. Hooper , School of Pharmacy , Sunderland Polytechnic , Sunderland , Co. Durham The polarographic reduction of a number of isatogens has been studied . The results show that the reduction ...
Contents
ISCHA 013 | 1034 |
Physical organic chemistry | 1035 |
Studies of the reactions of the anhydrosulphites of ahydroxycarboxylic acids Part IV Steric | 1044 |
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absorption acetic acid activation added addition alcohol Amer amine anhydrosulphite anion appears aqueous aromatic assigned atom attack bands base benzene bond buffer calculated carbon carbon tetrachloride Chem chloride compared compounds concentration conformation containing corresponding decomposition derived described determined discussed effect electron energy equation ester ether evidence excess expected experimental experiments factors Figure followed formation formed further gave give given hydrogen hydrolysis increase indicate interaction involving kinetic less measured mechanism method methyl MICHIGAN mixture molecular molecules nitrogen nucleophilic observed obtained occurs organic oxidation phenyl phosphate plot position possible prepared presence proton pyridine radical radical anion rate constants ratio reaction reactivity reduction relative reported requires respectively ring showed shown similar sodium solution solvent spectra spectrum splitting structure studied substituent suggested Table temperature transition University values yield