Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 371
... solution was heated for 0.5 hr . The product was obtained by cooling the solution , or upon rotary evaporation of the cooled solution . A similar , but more convenient , method of preparation involved heating a suspension of Cu ( sal ) ...
... solution was heated for 0.5 hr . The product was obtained by cooling the solution , or upon rotary evaporation of the cooled solution . A similar , but more convenient , method of preparation involved heating a suspension of Cu ( sal ) ...
Page 855
... solution becomes brown in a few hours . In acid medium there is no such observable colouration , and some authors have incorrectly taken this as a sign of the stability of ( I ) in acid solution . Lu Valle et al . have reported that ( I ) ...
... solution becomes brown in a few hours . In acid medium there is no such observable colouration , and some authors have incorrectly taken this as a sign of the stability of ( I ) in acid solution . Lu Valle et al . have reported that ( I ) ...
Page 859
... solution used as a filter for removing any lower wavelengths had no effect on the photolysis . While being irradiated the test solutions were kept cool at ca. 33 ° by a cold air blast , except for white light irradiation when samples ...
... solution used as a filter for removing any lower wavelengths had no effect on the photolysis . While being irradiated the test solutions were kept cool at ca. 33 ° by a cold air blast , except for white light irradiation when samples ...
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