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 474
... carbon tisulphide to give a niyıra 38 semag priems and ine red headles The atter presumably the runnydrone , m . p . 201 sould we sumonad y Siding the material along filter paper , when the needles adhered to the ilyas of he ymeT ...
... carbon tisulphide to give a niyıra 38 semag priems and ine red headles The atter presumably the runnydrone , m . p . 201 sould we sumonad y Siding the material along filter paper , when the needles adhered to the ilyas of he ymeT ...
Page 564
... Carbon disulphide Carbon tetrachloride ( α € 1 ) w1 = 0 ( B ) w0 , = 0 ∞P ( c.c. ) RD ( c.c. ) μ ( аpp . ) ( D ) -4.138 -0.255 38.8 26.2 * 0-78 -3.150 -0.079 57.1 44.2 0-79 -2.703 +0.020 73.5 62.3 0.74 - 2.560 +0.112 28.0 20.9 0.59 ...
... Carbon disulphide Carbon tetrachloride ( α € 1 ) w1 = 0 ( B ) w0 , = 0 ∞P ( c.c. ) RD ( c.c. ) μ ( аpp . ) ( D ) -4.138 -0.255 38.8 26.2 * 0-78 -3.150 -0.079 57.1 44.2 0-79 -2.703 +0.020 73.5 62.3 0.74 - 2.560 +0.112 28.0 20.9 0.59 ...
Page 572
... carbon - phosphorus bond , products in which halogen has been eliminated from both a- and ẞ - carbon atoms . Alkaline hydrolysis of polyfluoroalkylphosphonous dichlorides leads to the corresponding polyfluoroalkane , which is mixed with ...
... carbon - phosphorus bond , products in which halogen has been eliminated from both a- and ẞ - carbon atoms . Alkaline hydrolysis of polyfluoroalkylphosphonous dichlorides leads to the corresponding polyfluoroalkane , which is mixed with ...
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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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