Quarterly Journal of the Chemical Society of London, Part 3 |
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Page 2604
... Table 2 , and apply to the co - ordinates given in Table 1. No complete analysis of the thermal motion as defined by these parameters has been attempted , but it appears that on the average the values of the Debye temperature factor ( B ) ...
... Table 2 , and apply to the co - ordinates given in Table 1. No complete analysis of the thermal motion as defined by these parameters has been attempted , but it appears that on the average the values of the Debye temperature factor ( B ) ...
Page 2645
... Tables 4–7 in which k is the apparent first - order constant governing the production of halide or hydrogen ion . TABLE 4 . [ CH , Flo = 19.2 mmoles / 1 . , [ KI ]。= 80.04 mmoles / 1 . , T - = 5.78 x 10-7 sec . " 343.54 ° K , k -1 t ...
... Tables 4–7 in which k is the apparent first - order constant governing the production of halide or hydrogen ion . TABLE 4 . [ CH , Flo = 19.2 mmoles / 1 . , [ KI ]。= 80.04 mmoles / 1 . , T - = 5.78 x 10-7 sec . " 343.54 ° K , k -1 t ...
Page 3016
... ( Table 7 ) . TABLE 6. Oxidation of cyclohexanone in sulphuric acid : dependence of rate on = acidity , at 25 ° . 0.0565N , [ Ketone ] [ VV ] [ H3O + ] ( M ) 104 % ( sec . - 1 ) ( 104k ) / [ H2O + ] = 0.096м , ionic strength = 6м . 1.1 ...
... ( Table 7 ) . TABLE 6. Oxidation of cyclohexanone in sulphuric acid : dependence of rate on = acidity , at 25 ° . 0.0565N , [ Ketone ] [ VV ] [ H3O + ] ( M ) 104 % ( sec . - 1 ) ( 104k ) / [ H2O + ] = 0.096м , ionic strength = 6м . 1.1 ...
Contents
ABEL E W Bennett M A and Wilkinson G | 2323 |
Bourne E J Hartigan J and Weigel H | 2332 |
Clark E R | 2344 |
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1,3,5-trinitrobenzene absorption acetic acid acetic anhydride acetone added alcohol alkaline alkyl Amer amine ammonia anhydride atom benzene boiling bond bromide Calc carbon Chem chloride chloroform chromatography complex compound concentration constant cooled crystallised crystals curve decomp derivatives diethylamine dilute dimer dioxan dioxide dissolved distilled dried eluted ester ethanol evaporated filtered filtrate formation formed Found fraction gave give glycollic acid glyoxylic acid heated hydride hydrochloric acid hydrolysis hydroxide infrared infrared spectrum iodide isolated isomer K₁ light petroleum b. p. lithium lithium aluminium hydride m. p. and mixed methyl methyl iodide mixed m. p. mixture mole molecular molecule nitrogen obtained oxidation oxygen perchlorate picrate polymer potassium precipitate prepared prisms pyridine reaction reduced refluxed requires residue room temperature salt sodium hydroxide solid solvent spectra stirred structure sulphuric acid Table titration ultraviolet values washed yield