Journal of the Chemical Society, Part 1The Society., 1959 |
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Results 1-3 of 83
Page 400
... reactions in aqueous solution have been calculated in the hope of discovering which reaction is thermodynamically more probable . The thermodynamic treatment is described in detail in our previous paper.2 The standard free energies have ...
... reactions in aqueous solution have been calculated in the hope of discovering which reaction is thermodynamically more probable . The thermodynamic treatment is described in detail in our previous paper.2 The standard free energies have ...
Page 1193
... reaction vessels recently coated with a carbonaceous film by decomposition of allyl bromide , or in which inhibitors had been used , the reaction rate was irreproducible and invariably less than the rate previously reported . In a reaction ...
... reaction vessels recently coated with a carbonaceous film by decomposition of allyl bromide , or in which inhibitors had been used , the reaction rate was irreproducible and invariably less than the rate previously reported . In a reaction ...
Page 1195
... reaction , nevertheless prolonged the induction period in the chain mechanism sufficiently to enable the initial first - order rate coefficients of the maximally inhibited reaction to be measured . The lack of dependence of the rate ...
... reaction , nevertheless prolonged the induction period in the chain mechanism sufficiently to enable the initial first - order rate coefficients of the maximally inhibited reaction to be measured . The lack of dependence of the rate ...
Contents
3Dioxa and 1 3 | 1 |
Triterpenoids Part LVII The oxidation of norfriedelanone with selenium dioxide | 38 |
2dichloro3 4epoxybutane and related compounds | 44 |
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absorption acetic acid acetone acetyl chloride added alcohol alkaline alumina Amer amine anhydride aqueous sodium atom band benzene boiling bond bromide Calc carbonyl CHâ‚‚ Chem chloroform chromatography complex compound concentrated cooled crystallised cyclohexene decomp derivative dilute dioxan distilled dried electron eluted epoxide ester ethanol evaporated excess extracted with ether filtered filtrate fluoride formation formed Found fraction gave give heated under reflux hydrochloric acid hydrogen chloride hydrolysis hydroxyl ibid infrared spectrum iodide isolated isomers ketone lithium aluminium hydride m. p. and mixed methyl mixed m. p. mixture mmole molecule needles nitrate nitrogen nitrous acid obtained olefin oxidation oxygen peroxide picrate potassium hydroxide precipitate prepared pyridine radicals reaction reagent reduced requires residue room temperature salt separated sodium hydroxide solid solution solvent spectra structure sulphuric acid Table tetrachloride triethylamine ultraviolet values washed yellow yield