Journal of the Chemical Society, Part 5The Society., 1965 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
From inside the book
Results 1-3 of 76
Page 6462
... solution of hydrogen bromide in acetic acid ( 1 drop ) , and then titrated with a solution of bromine in acetic acid ( 10 ml .; 0.5 % v / v solution ; 1.05 mol . ) during 20 min.5 A solution of sodium hydrogen sulphite was added , and ...
... solution of hydrogen bromide in acetic acid ( 1 drop ) , and then titrated with a solution of bromine in acetic acid ( 10 ml .; 0.5 % v / v solution ; 1.05 mol . ) during 20 min.5 A solution of sodium hydrogen sulphite was added , and ...
Page 6794
... solution warmed until it became greenish - brown . Dimethylphenylphosphine ( 3.18 g . ) was added to the cold solution , which was then heated under reflux for 1 hr . and cooled , when a mixture of pink and yellow crystals separated ...
... solution warmed until it became greenish - brown . Dimethylphenylphosphine ( 3.18 g . ) was added to the cold solution , which was then heated under reflux for 1 hr . and cooled , when a mixture of pink and yellow crystals separated ...
Page 7470
... solution was evaporated to low volume . Potassium hydroxide ( 4 g . ) was then added , the solution was evaporated to dryness , and the residue heated at 112 ° for 4 hr . at 12 mm . Ether and water were then added and the ether ...
... solution was evaporated to low volume . Potassium hydroxide ( 4 g . ) was then added , the solution was evaporated to dryness , and the residue heated at 112 ° for 4 hr . at 12 mm . Ether and water were then added and the ether ...
Contents
6613 | 5783 |
Transitionmetal quinoxaline complexes Part II Copper1 derivatives | 5784 |
ptolyl | 5785 |
180 other sections not shown
Other editions - View all
Common terms and phrases
absorption acetic acid acetic anhydride acetone Amer amine anhydride aqueous atoms band benzene benzyl bond borazocine boron bromide Calc carbon carbon tetrachloride CH₂ Chem chloride chloroform chromatography cm.¹ colourless complex compounds concentration crystallised decomp derivatives dibromide dilute dissolved distilled elution ester ethanol ether ethyl acetate evaporated extracted filtered filtrate fluoride Found fraction gave give heated under reflux hydrochloric acid hydrogen hydrogen chloride hydrolysis hydroxide infrared infrared spectrum isolated isomer ketone ligand light petroleum m. p. and mixed methyl mixed m. p. mixture mmoles mole molecule n.m.r. spectrum nitrogen obtained olefin optical oxazolone oxide peak perchlorate phenyl potassium prepared protons pyridine Raney nickel reaction requires residue ring room temperature salt showed sodium sodium hydroxide solid solution solvent spectra structure sulphide sulphoxide sulphuric Table thionyl chloride vacuo values VIII yellow yield