Journal of the Chemical Society, Part 4Chemical Society., 1962 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
From inside the book
Results 1-3 of 58
Page 4511
... activity 0-794 μc / mmole ) . Energy input 5-3 × 1022 ev Carrier ( mmoles ) ( vol . 4 1. ) . HOCH , CHO 10.0 1.96 × 10-3 0.253 Product Spec . activity ( μc / mmole ) Yield ( mmole ) ( CH , OH ) , 323 1.53 x 10-2 63.8 Erythritol 4.09 7 ...
... activity 0-794 μc / mmole ) . Energy input 5-3 × 1022 ev Carrier ( mmoles ) ( vol . 4 1. ) . HOCH , CHO 10.0 1.96 × 10-3 0.253 Product Spec . activity ( μc / mmole ) Yield ( mmole ) ( CH , OH ) , 323 1.53 x 10-2 63.8 Erythritol 4.09 7 ...
Page 4658
... activity Unsatd . CO formed in products products Satd . products Involatile Temp . ( mm . ) ( 10-2 mmoles ) ( 10-6 ... activity of the acetone decomposed , calculated from the CO formed , it being assumed that each molecule of acetone ...
... activity Unsatd . CO formed in products products Satd . products Involatile Temp . ( mm . ) ( 10-2 mmoles ) ( 10-6 ... activity of the acetone decomposed , calculated from the CO formed , it being assumed that each molecule of acetone ...
Page 5173
... activity , had m . p . 246--247 ° , specific activity 6.5 μc per g . To a suspension of anhydrous sodium [ 2-14C ] acetate ( 62 mg .; 0.01 mc ) in pyridine ( 3 ml . ) at 5 ° was added toluene - p - sulphonyl chloride ( 140 mg . ) and ...
... activity , had m . p . 246--247 ° , specific activity 6.5 μc per g . To a suspension of anhydrous sodium [ 2-14C ] acetate ( 62 mg .; 0.01 mc ) in pyridine ( 3 ml . ) at 5 ° was added toluene - p - sulphonyl chloride ( 140 mg . ) and ...
Contents
Organic | 4261 |
NO PAGE | 4265 |
The synthesis of polycyclic aromatic hydrocarbons Part II Optical rotatory | 4268 |
58 other sections not shown
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Common terms and phrases
absorption acetic acid acetic anhydride acetone acetylacetone alcohol Amer anhydride aqueous atom b₁ band benzene bond bromide Calc carbon tetrachloride carbonyl CH₂ Chem chloroform chromatography cm.¹ CO₂H complex compound concentration constant cooled Cotton effect crystallised decomp derivative diethyl dilute dioxan distilled dried electron ester ethanol ether ethyl acetate ethylene evaporated experimental extracted filtered filtrate formed Found fraction gave give heated hydrochloric hydrogen chloride hydrolysis hydroxide infrared infrared spectrum k₁ ketone lactone ligand light petroleum b. p. measured methyl mixed m. p. mixture mmoles mole molecular molecule molybdenum needles nitrate nitrogen obtained oxidation peroxide phenyl polymer potassium precipitate prepared protons pyridine radicals reaction reduced refluxed requires residue resonance room temperature salt sample sodium sodium hydroxide solid solution solvent spectra steric structure substitution sulphide sulphuric acid t-butyl Table values washed yellow yield