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 4934
... initial stages of the reaction according to equations ( 1 ) , ( 2 ) , and ( 3 ) . They are formed more rapidly as ... initial rate of reaction of decaborane against the initial pressure of decaborane at a fixed initial pressure of ethyl ...
... initial stages of the reaction according to equations ( 1 ) , ( 2 ) , and ( 3 ) . They are formed more rapidly as ... initial rate of reaction of decaborane against the initial pressure of decaborane at a fixed initial pressure of ethyl ...
Page 4935
... initial rate of reaction of ethyl bromide against the initial pressure of decaborane . Values of k 。 are known from previous work , 2 and the values of ( k1k2 ) were obtained from Figs . 2-4 . It appears from a comparison of the 20 O ...
... initial rate of reaction of ethyl bromide against the initial pressure of decaborane . Values of k 。 are known from previous work , 2 and the values of ( k1k2 ) were obtained from Figs . 2-4 . It appears from a comparison of the 20 O ...
Page 5309
... initial concentration being appropriately adjusted . This procedure minimises systematic errors of timing ; it cannot be used satisfactorily for very fast runs , for which the initial concentration of bromine was obtained by titration ...
... initial concentration being appropriately adjusted . This procedure minimises systematic errors of timing ; it cannot be used satisfactorily for very fast runs , for which the initial concentration of bromine was obtained by titration ...
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