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 1290
... concentration of about 0.1M - hydrogen peroxide , proceeds with a convenient rate at 70 ° . The data were treated on the assumptions that the rate was ( i ) of first order dependence on bromomolybdate ( 11 ) concentration , ( ii ) ...
... concentration of about 0.1M - hydrogen peroxide , proceeds with a convenient rate at 70 ° . The data were treated on the assumptions that the rate was ( i ) of first order dependence on bromomolybdate ( 11 ) concentration , ( ii ) ...
Page 1690
... concentration of 5.1 x 10-3M and remains constant thereafter for at least a 25 - fold increase in concentration . At very much higher methoxide concentrations ( 1 · 5— 2.8M ) the absorption intensity at 4100 Å decreases , and this is ...
... concentration of 5.1 x 10-3M and remains constant thereafter for at least a 25 - fold increase in concentration . At very much higher methoxide concentrations ( 1 · 5— 2.8M ) the absorption intensity at 4100 Å decreases , and this is ...
Page 1701
... concentration regions in which E and F are found ( as there is in the similar case of methyl picrate 4 ) , but the concentration range of chief interest for the second complex is one where the h_ acidity function diverges significantly ...
... concentration regions in which E and F are found ( as there is in the similar case of methyl picrate 4 ) , but the concentration range of chief interest for the second complex is one where the h_ acidity function diverges significantly ...
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1-methylheptyl 1-phenylethyl bromide absorption acetic acid acetone acetonitrile adducts alcohol Amer amine anhydride aniline aqueous atom benzene bond Calc calculated carbon carboxyl Chem chloroform chromatography complex compounds concentration correlation crystallised cyclopropane derived diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether experimental extracted fluorine formation Found fraction gave H₂O halides hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum ionisation isomers k₁ k₂ kcal kinetic ligand methanolysis mixed m. p. mixture mmoles mole mole-¹ molecular molecules nitrogen nucleophilic o-complex obtained oleyl alcohol optical orbitals oxaloacetic acid oxidation oxygen peak phenols phosphate phosphine picryl potassium prepared proton pyridine rate coefficients rate constants reaction reflux requires residue rotation shown similar sodium solution solvent spectra structure substituted sulphide t-butyl methyl t-butyl peroxide Table tetracyanoethylene titration toluene-p-sulphonate values yield