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 1724
... hydroxide con- centration supervenes beyond ca. 4м . The spectrum of a solution of picric acid in 3 · 44m - sodium hydroxide after 15-8 days at 40 ° ( reaction half - life = 2.1 days ) showed maxima at 2700 and 3900 Å . Nitrite analyses ...
... hydroxide con- centration supervenes beyond ca. 4м . The spectrum of a solution of picric acid in 3 · 44m - sodium hydroxide after 15-8 days at 40 ° ( reaction half - life = 2.1 days ) showed maxima at 2700 and 3900 Å . Nitrite analyses ...
Page 1727
... Hydroxide . By V. GOLD and C. H. ROCHESTER . At low concentrations of sodium hydroxide in water , picramide reacts with one hydroxide ion , and dimethylpicramide with two hydroxide ions , to form soluble complexes . The corresponding ...
... Hydroxide . By V. GOLD and C. H. ROCHESTER . At low concentrations of sodium hydroxide in water , picramide reacts with one hydroxide ion , and dimethylpicramide with two hydroxide ions , to form soluble complexes . The corresponding ...
Page 2193
... hydroxide - calcium hydroxide . Aqueous sodium hydroxide was added to a solution of uscharidin ( 0.0054м , 5 ml . ) in dioxan - water ( 1 : 4 ) to bring the final volume to 10 ml . and to 0.005N with respect to alkali . The water used ...
... hydroxide - calcium hydroxide . Aqueous sodium hydroxide was added to a solution of uscharidin ( 0.0054м , 5 ml . ) in dioxan - water ( 1 : 4 ) to bring the final volume to 10 ml . and to 0.005N with respect to alkali . The water used ...
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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