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 4933
... Reaction ( 3 ) accounts for the fact that the rate of reaction of decaborane is faster than that of ethyl bromide . In the later stages of the reaction , both the decaborane and ethyl bromide curve show a much faster rate than would be ...
... Reaction ( 3 ) accounts for the fact that the rate of reaction of decaborane is faster than that of ethyl bromide . In the later stages of the reaction , both the decaborane and ethyl bromide curve show a much faster rate than would be ...
Page 4934
... reaction maintained by the ethyl bromide throughout the process is therefore due to reaction with the more active ethylated decaborane derivatives . It is not due to thermal decomposition of ethyl bromide 8 according to the equation C2H ...
... reaction maintained by the ethyl bromide throughout the process is therefore due to reaction with the more active ethylated decaborane derivatives . It is not due to thermal decomposition of ethyl bromide 8 according to the equation C2H ...
Page 5125
... ( reaction 20 ) and ethanol . It will be shown in Part II that reactions ( 4 ) and ( 5 ) are insignificant under our conditions , so that ( 7 ) must be the only ethanol - producing reaction ; however , whilst it may have a small activ ...
... ( reaction 20 ) and ethanol . It will be shown in Part II that reactions ( 4 ) and ( 5 ) are insignificant under our conditions , so that ( 7 ) must be the only ethanol - producing reaction ; however , whilst it may have a small activ ...
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