Journal of the Chemical Society, Part 2, Pages 1201-2488The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 1284
... mixture of this type . It is quite probable that such mixtures are not uncommon . Brooker 5 reported the isolation of an ester of ferulic acid , and considered the alcohol derived from it to be a mixture of ceryl and lignoceryl alcohols ...
... mixture of this type . It is quite probable that such mixtures are not uncommon . Brooker 5 reported the isolation of an ester of ferulic acid , and considered the alcohol derived from it to be a mixture of ceryl and lignoceryl alcohols ...
Page 2126
... mixture was heated slowly to 360 ° in a nitrogen atmosphere and maintained at 360 ° for 30 min . The cooled residue was ground with soda - lime ( 0 · 1 g . ) and covered with more soda - lime ( 0.1 g . ) . The mixture was heated slowly ...
... mixture was heated slowly to 360 ° in a nitrogen atmosphere and maintained at 360 ° for 30 min . The cooled residue was ground with soda - lime ( 0 · 1 g . ) and covered with more soda - lime ( 0.1 g . ) . The mixture was heated slowly ...
Page 2181
... mixture of the three isomers having the same composition as that found in the isomer - ratio determinations . A known weight of the mixture was then chromatographed , and the total amount of phenyl- pyridines present in the reaction mixture ...
... mixture of the three isomers having the same composition as that found in the isomer - ratio determinations . A known weight of the mixture was then chromatographed , and the total amount of phenyl- pyridines present in the reaction mixture ...
Contents
NO PAGE | 1205 |
The SN mechanism in aromatic compounds Part XXX The sydnone ring | 1213 |
NO PAGE | 1224 |
57 other sections not shown
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1-phenylethyl absorption acetic acid acetone acetonitrile adducts alcohol alginic acid Amer amine aniline aqueous atom benzene bond bromide Calc calculated carbon carboxyl CH₂ Chem chloride chloroform chromatography cm.¹ complex compounds concentration corresponding crystallised derived diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether evaporated experimental extracted fluorine formation formed Found fraction gave H₂O hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum iodide ionisation isomers k₁ k₂ kcal kinetic ligand methanolysis methyl mixed m. p. mixture mmoles mole mole-¹ molecule nitrogen nucleophilic o-complex obtained optical orbitals oxaloacetic acid oxidation oxygen peaks peroxide phenols phosphate phosphine potassium prepared proton pyridine rate coefficients reaction reduced reflux requires residue room temperature rotation shown similar sodium solution solvent spectra structure substituted sulphide sulphuric t-butyl Table tetracyanoethylene titration tricyanovinyl values yield