Journal of the Chemical SocietyThe Society., 1965 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 3223
... butene before about eighty percent removal of diene shows that butene was less strongly adsorbed than buta - 1,3 - diene . Studies of butene hydrogenation by the present authors , using catalyst samples from the same stocks , have shown ...
... butene before about eighty percent removal of diene shows that butene was less strongly adsorbed than buta - 1,3 - diene . Studies of butene hydrogenation by the present authors , using catalyst samples from the same stocks , have shown ...
Page 3226
... butene . Comparisons with Previous Work . - The initial butene distributions and selectivities obtained by using palladium and platinum in the present work are compared with results from other studies in Table 4. Strict comparisons of ...
... butene . Comparisons with Previous Work . - The initial butene distributions and selectivities obtained by using palladium and platinum in the present work are compared with results from other studies in Table 4. Strict comparisons of ...
Page 3227
... butene hydrogen- ation and hence butene desorption is again favoured relative to butane formation in the former reaction . The combined magnitude of these effects clearly varies from metal to metal ; it is considerable for palladium ...
... butene hydrogen- ation and hence butene desorption is again favoured relative to butane formation in the former reaction . The combined magnitude of these effects clearly varies from metal to metal ; it is considerable for palladium ...
Contents
By W GEE R A SHAW and B C SMITH | 3012 |
Organic | 3015 |
By DAVID PETERS | 3026 |
Copyright | |
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absorption acetic acid acetone added alcohol alumina Amer amine aqueous aromatic atom band benzene boron boron trichloride bromide butene butenolide Calc calculated carbonyl catalyst cation CH₂ Chem chloride chloroform chromatography cm.¹ CO₂Me complexes compounds concentration conjugated constants crystallised crystals delocalisation diluted dimethyl dimethylformamide dioxan distilled diyne dried electron eluted energy equilibrium ester ethanol ethyl acetate evaporated experimental extracted with ether Figure formation formed Found fraction frequency gave gibberellin give halides heated hexane hydrochloric hydrolysis hydroxide infrared infrared spectra iodide isomer isomerisation isoxazole ketone ligand light petroleum lophine method mixture molar mole molecular molecule needles nitrogen obtained orbitals oxidation peak petroleum b. p. phenyl piperidine polymers potassium prepared pressure proton pyridine reaction reflux requires residue resonance ring room temperature sodium hydrogen carbonate solid solution solvent spectrum structure Table ultraviolet values washed yield