Journal of the Chemical SocietyThe 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 82
Page 4885
... experimental value is 0.90 × 10-5 , and the difference of 30 % is well outside the experimental error . = With the values of a in Table 2 as a guide , we calculated log K as a function of 1 / ɛT for constant values of a = 4-5 , 4-6 ...
... experimental value is 0.90 × 10-5 , and the difference of 30 % is well outside the experimental error . = With the values of a in Table 2 as a guide , we calculated log K as a function of 1 / ɛT for constant values of a = 4-5 , 4-6 ...
Page 5106
... experimental values of x , and at values of x midway between each consecutive pair of experimental values . dx / dt was also evaluated at these points . In general , it was found that the lowest - order polynomial ( n 3 ) did not agree ...
... experimental values of x , and at values of x midway between each consecutive pair of experimental values . dx / dt was also evaluated at these points . In general , it was found that the lowest - order polynomial ( n 3 ) did not agree ...
Page 5107
... experimental . B , eqn . ( 7 ) . C , eqn . ( 16 ) . D , eqn . ( 17 ) . 4000 8000 Time ( sec . ) 12000 16000 DISCUSSION Table 1 shows that , for any one system containing solvent , the agreement between the equations tested and experiment ...
... experimental . B , eqn . ( 7 ) . C , eqn . ( 16 ) . D , eqn . ( 17 ) . 4000 8000 Time ( sec . ) 12000 16000 DISCUSSION Table 1 shows that , for any one system containing solvent , the agreement between the equations tested and experiment ...
Contents
NO PAGE | 4677 |
Water in hydrates Part II Light and heavy water and sulphur dioxide | 4684 |
sulphurcontaining antioxidants | 4692 |
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absorption acetic acid acetone added adduct aluminium chloride Amer amine anisole aqueous aromatic atoms band benzene bond boron trifluoride bromide Calc carbon cation CH₂ Chem chloride chromatography cm.¹ complex compound concentration constant cooled crystallised crystals decaborane decomposition derivatives dilute dimethyl dioxide distilled dried eluted ester ethanol ether evaporated experimental extracted filtered formation formed Found fraction gave give H₂O hydride hydrochloric acid hydrogen hydrolysis hydroxide hydroxyl infrared infrared spectrum iodide isolated isomer ketone ligand light petroleum b. p. lithium aluminium hydride methyl methylene mixture mole molecular molecules needles nitrate nitrogen obtained olefin oxide penten peroxide phenol potassium precipitate prepared pressure protons pyridine radical ratio reaction recrystallised reduced requires residue resonance room temperature salt sample silver sodium sodium hydroxide solid solubility solution solvent spectra structure sulphuric Table values washed yellow yield