Quarterly Journal of the Chemical Society of London, Part 1, Pages 1-1200 |
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Page 152
... chloride , to form hydrogen chloride and methane as the main gaseous products ( approximately one mole of each per mole of compound decomposed ) . DISCUSSION The product analysis in Table 1 can be interpreted in terms of the ...
... chloride , to form hydrogen chloride and methane as the main gaseous products ( approximately one mole of each per mole of compound decomposed ) . DISCUSSION The product analysis in Table 1 can be interpreted in terms of the ...
Page 532
... chloride . The first part of the reaction represents the isomeric rearrange- ment of 1 - phenylallyl chloride to cinnamyl chloride ; the second concerns the reaction of the latter with triethylamine . First - order rate constants ...
... chloride . The first part of the reaction represents the isomeric rearrange- ment of 1 - phenylallyl chloride to cinnamyl chloride ; the second concerns the reaction of the latter with triethylamine . First - order rate constants ...
Page 666
... chloride was prepared by rearrangement of camphene hydrochloride in dry , refluxing methylene chloride , or more conveniently in liquid sulphur dioxide . It could also be prepared by passing dry hydrogen chloride into a solution of ...
... chloride was prepared by rearrangement of camphene hydrochloride in dry , refluxing methylene chloride , or more conveniently in liquid sulphur dioxide . It could also be prepared by passing dry hydrogen chloride into a solution of ...
Contents
Preparation and reactions of some oxoalkyliron complexes | 1 |
Developments in the theory of cationic polymerisation Part IV A general | 16 |
The lowfrequency infrared spectra of some complex halides of zinc cadmium | 26 |
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absorption acetic acid acetic anhydride alkaline aluminium aluminium chloride Amax Amer amine ammonia aqueous aromatic atom band benzene bond bromide Calc carbon CH₂ Chem chloride chloroform chromatography cm.¹ complex compound concentration coupling constants crystallised crystals decomp decomposition derivative dilute dimethyl dimethyl ether distilled dried Elution equation erythroaphins ester ethanol ether ethyl acetate evaporated EXPERIMENTAL extracted filtered fluoride formation Found fraction gave halides heated hydrochloric acid hydrogen hydrolysis infrared infrared spectra iodide K₁ ligand light petroleum lithium aluminium hydride log ɛ m. p. and mixed maltose method mixed m. p. mixture mole molecules nitrogen obtained oxidation oxygen phenyl picrate potassium precipitate prepared proton pyridine quinone reaction recrystallised refluxed requires residue resonance room temperature salt sample sodium hydroxide solution solvent spectrum structure substitution Table ultraviolet values washed yield