Journal of the Chemical Society, Part 2, Pages 1201-2488The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
From inside the book
Results 1-3 of 75
Page 1324
... relative selectivities it appeared that the fluorine atom or the tri- fluoromethyl group have no effect on the rate of halogenation at the terminal & carbon atom and very little influence at the y position . In order to calculate ...
... relative selectivities it appeared that the fluorine atom or the tri- fluoromethyl group have no effect on the rate of halogenation at the terminal & carbon atom and very little influence at the y position . In order to calculate ...
Page 1470
... relative to silanes on tritolyl phosphate columns ( polar phase ) than on Silicone 702 ( non - polar phase ) ... relative retention time are of great practical value in the isolation of individual silicon - germanium hydrides . 10 ( ii ) ...
... relative to silanes on tritolyl phosphate columns ( polar phase ) than on Silicone 702 ( non - polar phase ) ... relative retention time are of great practical value in the isolation of individual silicon - germanium hydrides . 10 ( ii ) ...
Page 1683
... relative rate constants under similar experimental conditions , and at 275 ° found kg / k1 = 1.41 which corresponds well with the value ( 1 · 35 ) obtained from our Arrhenius plot . Comparison of Reactivities of Sodium and Potassium ...
... relative rate constants under similar experimental conditions , and at 275 ° found kg / k1 = 1.41 which corresponds well with the value ( 1 · 35 ) obtained from our Arrhenius plot . Comparison of Reactivities of Sodium and Potassium ...
Contents
NO PAGE | 1205 |
The SN mechanism in aromatic compounds Part XXX The sydnone ring | 1213 |
NO PAGE | 1224 |
57 other sections not shown
Other editions - View all
Common terms and phrases
1-phenylethyl absorption acetic acid acetone acetonitrile adducts alcohol alginic acid Amer amine aniline aqueous atom benzene bond bromide Calc calculated carbon carboxyl CH₂ Chem chloride chloroform chromatography cm.¹ complex compounds concentration corresponding crystallised derived diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether evaporated experimental extracted fluorine formation formed Found fraction gave H₂O hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum iodide ionisation isomers k₁ k₂ kcal kinetic ligand methanolysis methyl mixed m. p. mixture mmoles mole mole-¹ molecule nitrogen nucleophilic o-complex obtained optical orbitals oxaloacetic acid oxidation oxygen peaks peroxide phenols phosphate phosphine potassium prepared proton pyridine rate coefficients reaction reduced reflux requires residue room temperature rotation shown similar sodium solution solvent spectra structure substituted sulphide sulphuric t-butyl Table tetracyanoethylene titration tricyanovinyl values yield