Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 340
... sulphuric acid was as follows . 98 % Sulphuric acid ( 0-85 ml . ) was added to water ( 0.22 ml . ) containing 22 atoms % excess of oxygen - 18 and also 23 atoms % excess of deuterium so that the resultant acid was 85 % sulphuric acid ...
... sulphuric acid was as follows . 98 % Sulphuric acid ( 0-85 ml . ) was added to water ( 0.22 ml . ) containing 22 atoms % excess of oxygen - 18 and also 23 atoms % excess of deuterium so that the resultant acid was 85 % sulphuric acid ...
Page 344
Chemical Society (Great Britain). in both sulphuric acid and perchloric acid , and is somewhat faster in sulphuric acid than in perchloric acid of equivalent acidity . Activation parameters for both stages of the re- arrangement of 2,4,6 ...
Chemical Society (Great Britain). in both sulphuric acid and perchloric acid , and is somewhat faster in sulphuric acid than in perchloric acid of equivalent acidity . Activation parameters for both stages of the re- arrangement of 2,4,6 ...
Page 351
... sulphuric para a acid at 25.0 ° , with [ HNO3 ] = 9 × 10м and [ CH , F2 - p ] 2 × 10 4м , ka 5 · 3 1. mole ̄1 sec. ̄1 ) , but the u.v. extinction curve of the product after 12 half - lives did not correspond fully with that of 2,5 ...
... sulphuric para a acid at 25.0 ° , with [ HNO3 ] = 9 × 10м and [ CH , F2 - p ] 2 × 10 4м , ka 5 · 3 1. mole ̄1 sec. ̄1 ) , but the u.v. extinction curve of the product after 12 half - lives did not correspond fully with that of 2,5 ...
Contents
Physical organic chemistry | 1 |
Topochemistry Part XXX Crystal and molecular structures of chalcone | 11 |
Conformational studies Part I Crystal and molecular structures of cis12dipchlorobenzoyl and cis | 17 |
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acetic acid activation added addition alcohol Amer angle appears aqueous assumed ation atoms base benzene bond bromination calculated carbon carbon tetrachloride Chem chemical Chemistry chloride compared complex compounds concentration conformation containing corresponding coupling crystal dependence derivatives determined difference DISCUSSION effect elimination energy equation error estimated ethanol ether exchange expected experimental experiments Figure formation fraction give given hydrogen increase indicators interaction intermediate involving isomer isotope kinetic measured mechanism method methyl mixture mole molecular molecule observed obtained occurs oxide oxygen parameters Phys plot position possible prepared present proton radical range rate constants ratio reaction reasonable relative reported requires respectively ring shifts shown shows similar sodium solution solvent spectra spectrum structure substituents suggested sulphuric Table temperature transition University values wave yield