Quarterly Journal of the Chemical Society of London |
From inside the book
Results 1-3 of 84
Page 1069
... Solvent A moves , therefore , from left to right and solvent B contrariwise . The problems to be solved first are the behaviour of a solute placed in any one vessel , and the possibility of separating solutes , the distribution ...
... Solvent A moves , therefore , from left to right and solvent B contrariwise . The problems to be solved first are the behaviour of a solute placed in any one vessel , and the possibility of separating solutes , the distribution ...
Page 1383
... solvent the main reaction is chlorination ; in solution it is iodination . Iodine monobromide always acts as a brominating agent . The relation between such reactions and the physical properties of the solvents and reactants is ...
... solvent the main reaction is chlorination ; in solution it is iodination . Iodine monobromide always acts as a brominating agent . The relation between such reactions and the physical properties of the solvents and reactants is ...
Page 1743
... solvent passes along the system continuously is considered . It is shown that the solute moves in the form of a wave ... solvent . B = " static " solvent . " volume , although this is not essential ; each vessel contains the same volume ...
... solvent passes along the system continuously is considered . It is shown that the solute moves in the form of a wave ... solvent . B = " static " solvent . " volume , although this is not essential ; each vessel contains the same volume ...
Other editions - View all
Common terms and phrases
absorption acetic anhydride acetone acetyl added alcohol alkaline alunite Amer amine ammonia anhydrous anilide aqueous sodium atom benzene boiling bromine trifluoride Calc carbonate CHâ‚‚ Chem chloroform colour colourless needles compound condensation containing cooled crystallised crystals cyanide cyclisation D.Sc decomp derivatives dilute dissolved distilled dried equiv ester ethanol ethyl acetate evaporated EXPERIMENTAL extracted with ether filtered filtrate fluoride formation formed Found fraction gave give heated under reflux hydrochloric acid hydrogen chloride hydrolysis iodide iodine ions isolated kcals ketone light petroleum b. p. liquid melting method methyl minutes mixed m. p. molecule nitrate nitrile nitrogen obtained oxalate oxide oxime oxygen pickeringite picrate piperidine potassium potassium hydroxide precipitate prepared prisms pyridine reductive dissolution removed requires residue room temperature salt semicarbazone separated sodium hydroxide solid soluble solvent specimen sulphate sulphuric acid values washed xylose yellow needles yield