Quarterly Journal of the Chemical Society of London, Part 3 |
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Page 2395
... methyl iodide ( 0.1 ml . ) , set aside at 20 ° for 2 days , gave yellow 8 - methylthioquinoline hydriodide , m . p . 196—197.5 ° ( from ethanol ) ( Found : C , 39-4 ; H , 3.3 ; N , 4.6 . C10H10NIS requires C , 39-6 ; H , 3-3 ; N , 4.6 ...
... methyl iodide ( 0.1 ml . ) , set aside at 20 ° for 2 days , gave yellow 8 - methylthioquinoline hydriodide , m . p . 196—197.5 ° ( from ethanol ) ( Found : C , 39-4 ; H , 3.3 ; N , 4.6 . C10H10NIS requires C , 39-6 ; H , 3-3 ; N , 4.6 ...
Page 2640
... methyl iodide and potassium cyanide in aqueous solution is shown to be irreversible , bimolecular , and free from ... methyl iodide were made up in conductivity water that had been freed from dissolved gases ; known volumes of the ...
... methyl iodide and potassium cyanide in aqueous solution is shown to be irreversible , bimolecular , and free from ... methyl iodide were made up in conductivity water that had been freed from dissolved gases ; known volumes of the ...
Page 2644
... Iodide and between Methyl Iodide and Potassium Chloride in Aqueous Solution . - The ratio kak2 K was first determined for this system by ascertaining the position of the minimum concentration of the halide ion originally present , for ...
... Iodide and between Methyl Iodide and Potassium Chloride in Aqueous Solution . - The ratio kak2 K was first determined for this system by ascertaining the position of the minimum concentration of the halide ion originally present , for ...
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