Journal of the Chemical SocietyThe Society., 1948 |
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Page 67
... carbon monoxide and quinol could be recovered from the solution . It melted at 170 ° also with liberation of carbon monoxide . That it is not simply a compound of carbon monoxide and quinol was shown by analysis , by failure to prepare ...
... carbon monoxide and quinol could be recovered from the solution . It melted at 170 ° also with liberation of carbon monoxide . That it is not simply a compound of carbon monoxide and quinol was shown by analysis , by failure to prepare ...
Page 71
... carbon dioxide an aqueous solution gives crystals of a - quinol containing no carbon dioxide . This is attributed to the low concentration of carbon dioxide , the quinol adopting the compact x - structure as it does when crystallised ...
... carbon dioxide an aqueous solution gives crystals of a - quinol containing no carbon dioxide . This is attributed to the low concentration of carbon dioxide , the quinol adopting the compact x - structure as it does when crystallised ...
Page 201
... Carbon Disulphide . By A. H. COOK , SIR IAN HEILBRON , and A. L. LEVY . Pure aminoacetonitrile and carbon disulphide under selected neutral conditions give 5 - amino - 2 - mercaptothiazole ( XI ) , whereas in presence of acetone the ...
... Carbon Disulphide . By A. H. COOK , SIR IAN HEILBRON , and A. L. LEVY . Pure aminoacetonitrile and carbon disulphide under selected neutral conditions give 5 - amino - 2 - mercaptothiazole ( XI ) , whereas in presence of acetone the ...
Contents
kilocals as the free energy difference contributed by the hyperconjugated methyl group | 373 |
SIR WILLIAM RAMSAY AND Ralph Forster LABORATORIES | 417 |
control of anionotropic rearrangement and of the significance of conjugation and hypercon | 440 |
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Common terms and phrases
4-dideuterobenzene absorption spectrum acetic acid acetic anhydride acetone added alkaline Amer ammonia analcite aqueous sodium atoms bands benzene boiling bond bromine Calc carbon catalyst CH₂ chabazite Chem chloride chloroform colourless needles compound concentrated cooled corresponding crystallised from alcohol crystals cyanide D.Sc decomp derivative dilute dissolved distilled dried electronic origin energy ester ethanol ether evaporated excited extracted filtered filtrate fluorescence formed Found fraction fundamental frequencies gave give H₂O heated hexadeuterobenzene hydrochloric acid hydrogen hydrogen chloride hydrolysis Ingold isolated kcals ketone light petroleum method methyl alcohol mixed m. p. mixture molecule obtained oxidation peroxide phenol potassium potassium hydroxide precipitated prepared prisms pyridine reaction reduced pressure refluxed requires residue room temperature salt separated sodium hydroxide solid soluble solution solvent spectra structure sulphide sulphuric acid symmetry transitions unsaturated upper electronic upper-state vibration washed yellow needles yield