Journal of the Chemical Society, Part 3, Pages 2489-3512The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 2608
Chemical Society (Great Britain). iodine monochloride - thionyl chloride ( 12 ml .; 23 % w / v ) , was added to uranium pentachloride in thionyl chloride ( 30 ml .; 0.13м ) . The precipitate was washed with thionyl chloride ( 10 ml ...
Chemical Society (Great Britain). iodine monochloride - thionyl chloride ( 12 ml .; 23 % w / v ) , was added to uranium pentachloride in thionyl chloride ( 30 ml .; 0.13м ) . The precipitate was washed with thionyl chloride ( 10 ml ...
Page 3017
... Thionyl Chloride . By K. W. BAGNALL , D. BROWN , and R. COLTON . The action of thionyl chloride on rhenium heptoxide and ammonium per - rhenate produces the sulphuryl chloride complexes , ( ReO , Cl ) 2 , SO , Cl , and ( NH4 ) 2ReO2Cl ...
... Thionyl Chloride . By K. W. BAGNALL , D. BROWN , and R. COLTON . The action of thionyl chloride on rhenium heptoxide and ammonium per - rhenate produces the sulphuryl chloride complexes , ( ReO , Cl ) 2 , SO , Cl , and ( NH4 ) 2ReO2Cl ...
Page 3018
... chloride , since thionyl chloride on hydrolysis would produce sulphite which requires oxidation ( e.g. , by bromine water ) before precipitation occurs with barium in acid media . The infrared spectrum shows no absorption around 1230 cm ...
... chloride , since thionyl chloride on hydrolysis would produce sulphite which requires oxidation ( e.g. , by bromine water ) before precipitation occurs with barium in acid media . The infrared spectrum shows no absorption around 1230 cm ...
Contents
Fluorocarbohydrates Part VIII Formation of halogenoderivatives from | 2493 |
Steric influences in radical reactions Part I Benzyl radicals derived from cyclic | 2500 |
56dioisopropylidene | 2514 |
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absorption acetic acid acetone added adduct alcohol Amax Amer aqueous aromatic ation atom atomic orbitals band benzene bond bromide Calc carbon carbonyl CH₂ Chem chloroform chromatography cm.¹ complex compound concentrated cooled crystallised cyclic cyclohexane decomp decomposition dilute dioxide distilled dried electron elution ester ethanol ether ethyl acetate evaporated extracted filtered filtrate formation formed Found fraction gave give heated hydrochloric hydrogen hydrogen chloride hydrolysis hydroxide infrared infrared spectrum ionisation energies isolated isomer ketone kinetic light petroleum mechanism methyl mixed m. p. mixture mole molecular molecule nitrate nitric nitric oxide nitrogen Nujol obtained oxide oxime perchlorate petroleum b. p. polymer potassium potassium hydroxide prepared proton pyridine reaction rearrangement reduced refluxed requires residue room temperature salt sodium solid solution solvent spectra structure sulphuric acid Table thionyl chloride transition ultraviolet values Vmax yellow yield