Journal of the Chemical SocietyThe Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 188
... solution was prepared , by weight , from acetic acid , potas- sium hydroxide solution , potassium chloride , and water . A stock solution of creatinine hydro- chloride was also prepared by weight . A series of eight experimental solutions ...
... solution was prepared , by weight , from acetic acid , potas- sium hydroxide solution , potassium chloride , and water . A stock solution of creatinine hydro- chloride was also prepared by weight . A series of eight experimental solutions ...
Page 964
... solution ) , 365. CIIrKO requires I , 66-2 ; Ir , 25.0 ; CO , 3.6 % ; M , 767 ] ; molar conductance ( 10 ̃3м - solution in acetone at 30 ° ) , 171 · 3 ohm1 . Tetraphenylarsonium Tetraiodocarbonyliridate ( 111 ) , ( AsPh ̧ ) [ IrI ( CO ) ...
... solution ) , 365. CIIrKO requires I , 66-2 ; Ir , 25.0 ; CO , 3.6 % ; M , 767 ] ; molar conductance ( 10 ̃3м - solution in acetone at 30 ° ) , 171 · 3 ohm1 . Tetraphenylarsonium Tetraiodocarbonyliridate ( 111 ) , ( AsPh ̧ ) [ IrI ( CO ) ...
Page 1062
... solution of perrhenic acid ( 1 g . ) and concentrated hydrochloric acid ( 1 ml . ) in ethanol ( 10 ml . ) , and the mixture boiled for 3-5 min . The yellow crystals were recrystallised ( benzene ) , giving the compound ( 2-6 g . , 78 ...
... solution of perrhenic acid ( 1 g . ) and concentrated hydrochloric acid ( 1 ml . ) in ethanol ( 10 ml . ) , and the mixture boiled for 3-5 min . The yellow crystals were recrystallised ( benzene ) , giving the compound ( 2-6 g . , 78 ...
Contents
NO PAGE | 1 |
Nucleophilic reactivity Part IV Competing bimolecular substitution | 5 |
The biosynthesis of fungal metabolites Part I Two different pathways | 16 |
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Common terms and phrases
absorption acetic acid alkaline aluminium chloride Amer amine anhydride aphins aqueous aromatic atoms band benzene bond bromide Calc carbon Chem chloride chloroform chromatography cm.¹ complex compound concentration coupling constants crystallised crystals decomp decomposition derivatives diazomethane dilute dimethyl dimethyl ether dioxan dried Elution equation erythroaphin-fb erythroaphins ester ethanol ether ethyl ethyl acetate evaporated EXPERIMENTAL extracted formation Found fraction gave halides hydrochloric acid hydrogen hydrogen chloride hydrolysis infrared infrared spectra iodide irradiated isomer k₂ ligand light petroleum m. p. and mixed maltose mixed m. p. mixture mole molecule mµ log ɛ nitrogen obtained oxidation oxygen phenyl piperidine potassium precipitate prepared protoaphin proton pyridine quinone reaction recrystallised refluxed requires residue room temperature sample similar sodium hydroxide soluble solution solvent spectrum structure substitution Table ultraviolet values washed yellow yield