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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Results 1-3 of 76
Page 3698
... Table 3 are shown in Table 4. The mean value , 6-1 x 10-3 1.3 mole 3 sec . - 1 , was used for k''N . Also shown in Table 4 are corrected A / N ratios , i.e. , k ̧ / k 、 values . TABLE 4 . Concurrent acetoxylation and nitration of m ...
... Table 3 are shown in Table 4. The mean value , 6-1 x 10-3 1.3 mole 3 sec . - 1 , was used for k''N . Also shown in Table 4 are corrected A / N ratios , i.e. , k ̧ / k 、 values . TABLE 4 . Concurrent acetoxylation and nitration of m ...
Page 3878
... Table 3 and xp / c , having a value necessary for a plot of R / A , against Am / A , to be a straight line of which the intercept is x / c , and the slope xm / cm . The results are depicted in Table 5 . TABLE 5 . Percentages of isomers ...
... Table 3 and xp / c , having a value necessary for a plot of R / A , against Am / A , to be a straight line of which the intercept is x / c , and the slope xm / cm . The results are depicted in Table 5 . TABLE 5 . Percentages of isomers ...
Page 3912
... Table 10 . TABLE 10 . 21 Effects of various salts on the first - order rate - constants of racemisation of ( — ) - a - carb- ethoxybenzylmercuric bromide ( initial rotation [ x ] -11.8 in acetone ; c = 1.0 % w / v ) in dimethyl ...
... Table 10 . TABLE 10 . 21 Effects of various salts on the first - order rate - constants of racemisation of ( — ) - a - carb- ethoxybenzylmercuric bromide ( initial rotation [ x ] -11.8 in acetone ; c = 1.0 % w / v ) in dimethyl ...
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