Journal of the Chemical SocietyThe Society., 1950 |
From inside the book
Results 1-3 of 72
Page 123
... complex ion and , in addition , more than one R group may be lost by the complex ion , leading to further equilibria involving water and the anion . The extent to which the last two groups enter the co - ordination sphere depends on the ...
... complex ion and , in addition , more than one R group may be lost by the complex ion , leading to further equilibria involving water and the anion . The extent to which the last two groups enter the co - ordination sphere depends on the ...
Page 128
... complex as a fine white or very pale green powder . A simple apparatus was devised for filtering off these compounds in the absence of air ( see p . 130 ) . Cuprous iodide complexes are stable in air and are formed when cuprous iodide ...
... complex as a fine white or very pale green powder . A simple apparatus was devised for filtering off these compounds in the absence of air ( see p . 130 ) . Cuprous iodide complexes are stable in air and are formed when cuprous iodide ...
Page 848
... complex dissolved readily in chloroform or benzene on shaking and was fairly soluble in acetone and warm alcohol . From the alcoholic solution the bisarsine compound was precipitated on cooling unless excess of arsine was present . The ...
... complex dissolved readily in chloroform or benzene on shaking and was fairly soluble in acetone and warm alcohol . From the alcoholic solution the bisarsine compound was precipitated on cooling unless excess of arsine was present . The ...
Other editions - View all
Common terms and phrases
4-dione absorption acetic acid acetic anhydride acetone acetyl activity added alcohol alkaline Amer amine ammonia amylose anhydride atom benzene boiling bromide bromine trifluoride Calc carbon dioxide carbon tetrachloride catalyst CH₂ Chem chloride chloroform CO₂ colour colourless complex compound cooling corresponding crystallised crystals cyclisation D.Sc decomp derivatives diazomethane dilute dioxan dissolved distilled disulphide dried electron ester ethanol ether ethyl acetate ethylamine evaporated extracted filtered filtrate formed Found fraction gave give heated under reflux hydrochloric acid hydrogen chloride hydrolysis iodide isolated ketone light petroleum b. p. liquid m. p. and mixed metals method methyl minutes mixed m. p. mixture molecule needles nitrate obtained oxidation potassium precipitate prepared prisms pyridine Q-enzyme reaction reagent reduced requires residue room temperature salt separated sodium hydroxide solid soluble solution solvent sulphate sulphide sulphuric acid washed yellow yield