Journal of the Chemical SocietyThe Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 4896
... present Paper . 8 The y region represents a single phase consisting of the metal hydride containing " dis- solved " metal . The many published studies of transition metal hydrides leave no doubt that equilibrium pressures can be ...
... present Paper . 8 The y region represents a single phase consisting of the metal hydride containing " dis- solved " metal . The many published studies of transition metal hydrides leave no doubt that equilibrium pressures can be ...
Page 4933
... present system ; its rate of reaction is ~ 2.5 times faster . The main products are 1,2 - diethyldecaborane , 2,4 - diethyldecaborane , decaborane , hydrogen , and methane . Decaborane was present in relatively low concentrations , and ...
... present system ; its rate of reaction is ~ 2.5 times faster . The main products are 1,2 - diethyldecaborane , 2,4 - diethyldecaborane , decaborane , hydrogen , and methane . Decaborane was present in relatively low concentrations , and ...
Page 5097
... present in the original ketone and hydrogenation does not introduce another . It follows that hydrogenation affects an olefinic system . Attempts at selective oxidation failed , the cycloheptaindole either resisting or dis- integrating ...
... present in the original ketone and hydrogenation does not introduce another . It follows that hydrogenation affects an olefinic system . Attempts at selective oxidation failed , the cycloheptaindole either resisting or dis- integrating ...
Contents
NO PAGE | 4677 |
Water in hydrates Part II Light and heavy water and sulphur dioxide | 4684 |
sulphurcontaining antioxidants | 4692 |
Copyright | |
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absorption acetic acid acetone added adduct aluminium chloride Amer amine anisole aqueous aromatic atoms band benzene bond boron trifluoride bromide Calc carbon cation CH₂ Chem chloride chromatography cm.¹ complex compound concentration constant cooled crystallised crystals decaborane decomposition derivatives dilute dimethyl dioxide distilled dried eluted ester ethanol ether evaporated experimental extracted filtered formation formed Found fraction gave give H₂O hydride hydrochloric acid hydrogen hydrolysis hydroxide hydroxyl infrared infrared spectrum iodide isolated isomer ketone ligand light petroleum b. p. lithium aluminium hydride methyl methylene mixture mole molecular molecules needles nitrate nitrogen obtained olefin oxide penten peroxide phenol potassium precipitate prepared pressure protons pyridine radical ratio reaction recrystallised reduced requires residue resonance room temperature salt sample silver sodium sodium hydroxide solid solubility solution solvent spectra structure sulphuric Table values washed yellow yield