Journal of the Chemical Society, Part 4, Pages 3513-4668The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 3751
... atoms near ( 1 ) . Further calculations using these positions proved reasonably satisfactory when pairs of half - atoms were used to approximate the elliptical shapes of the peaks , and when the atomic scattering factors were reduced ...
... atoms near ( 1 ) . Further calculations using these positions proved reasonably satisfactory when pairs of half - atoms were used to approximate the elliptical shapes of the peaks , and when the atomic scattering factors were reduced ...
Page 4398
... atom was placed arbitrarily at y = 1.0 . The x- and z - co - ordinates of the two bromine atoms were obtained from the ( 010 ) projection of the Patterson function . The y - co - ordinate of the second bromine atom was determined by ...
... atom was placed arbitrarily at y = 1.0 . The x- and z - co - ordinates of the two bromine atoms were obtained from the ( 010 ) projection of the Patterson function . The y - co - ordinate of the second bromine atom was determined by ...
Page 4468
... atoms occurs in all the octa - amino- compounds , the differences in ApK , and ApK , ' among individual compounds being due to other effects . The evidence that the first proton in the cases of both the tri- and tetra - phosphazenes ...
... atoms occurs in all the octa - amino- compounds , the differences in ApK , and ApK , ' among individual compounds being due to other effects . The evidence that the first proton in the cases of both the tri- and tetra - phosphazenes ...
Contents
4028 | 3507 |
Nucleophilic reactivity | 3513 |
Molecular polarisability Dipole moments molar Kerr constants and apparent | 3523 |
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absorption acetic acid acetic anhydride acetone acetoxylation acetyl added alcohol alkaline alumina aluminium Amer amine atoms band benzene benzyl bond bromide Calc carbon carbonyl chabazite Chem chloride chloroform chromatography cm.¹ compounds concentration crystals decomp diethyl diluted dimethylformamide diol dissolved distilled dried ester ethanol ethyl acetate evaporated EXPERIMENTAL extracted with ether filtrate formation Found fraction gave give heated hydrochloric acid hydrochloride hydrogen hydrolysis hydroxyl infrared iodide isomers K₁ ketone light petroleum lithium lithium aluminium hydride log ɛ m. p. and mixed mixed m. p. mixture mole molecules needles nitrate nitric acid nitrogen o-xylene obtained optical oxide oxygen petroleum b. p. phenol picrate potassium precipitated prepared proton pyridine rate constants reaction recrystallised refluxed requires residue room temperature salt sodium hydroxide solvent spectra spectrum stirred structure substitution sulphuric acid Table values washed yield