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 1302
... Infrared spectrum : 1439vs , 1200m , 1189sh , 1117s , 1064s , 1047ms , 1026ms , 999m , 800m , 750s , 746sh , 727vs , 715vs , 691vs , 678sh , 656sh , 629ms , 612ms , 568m , 548m , 517vs , 454m , 403m , 355s , 333ms . Dimethylgallium ...
... Infrared spectrum : 1439vs , 1200m , 1189sh , 1117s , 1064s , 1047ms , 1026ms , 999m , 800m , 750s , 746sh , 727vs , 715vs , 691vs , 678sh , 656sh , 629ms , 612ms , 568m , 548m , 517vs , 454m , 403m , 355s , 333ms . Dimethylgallium ...
Page 1641
... infrared spectroscopy , and we now find that the infrared spectrum of the extremely deliquescent " chloroplatinic acid dihydrate " shows conclusively that hydroxonium ions are present . Results are presented in Table 1 , with ranges of ...
... infrared spectroscopy , and we now find that the infrared spectrum of the extremely deliquescent " chloroplatinic acid dihydrate " shows conclusively that hydroxonium ions are present . Results are presented in Table 1 , with ranges of ...
Page 1929
... infrared spectrum with those of mixtures of the two esters . Hydrogen chloride used Product Run ( mmoles ) ( Equiv . compared with acetoxy - ester ) 1 2.87 1.0 Temp . Room temp . ND 20 % hydroxy - ester 1.4190 15 2 11.5 4.0 Room temp ...
... infrared spectrum with those of mixtures of the two esters . Hydrogen chloride used Product Run ( mmoles ) ( Equiv . compared with acetoxy - ester ) 1 2.87 1.0 Temp . Room temp . ND 20 % hydroxy - ester 1.4190 15 2 11.5 4.0 Room temp ...
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Common terms and phrases
1-methylheptyl 1-phenylethyl bromide absorption acetic acid acetone acetonitrile adducts alcohol alginic acid Amer amine anhydride aniline aqueous atom benzene bond Calc calculated carbon Chem chloride chloroform CHPh chromatography cm.¹ complex compounds concentration crystallised cyanohydrin derivative diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether evaporated EXPERIMENTAL extracted formation formed Found fraction gave H₂O halides hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum isomers k₁ k₂ kcal ketone kinetic ligand magnesium manganese(III methanolysis methyl mixed m. p. mixture mmoles mole mole-¹ molecule nitrogen nucleophilic o-complex obtained optical oxaloacetic acid oxidation peaks peroxide petroleum b. p. phenols phosphate phosphine picryl potassium prepared proton pyridine rate coefficients reaction reflux requires residue room temperature rotation shown silanes sodium solution solvent spectra structure substituted sulphide sulphuric Table tetracyanoethylene titration tricyanovinyl values yield