Journal of the Chemical SocietyThe Society., 1954 |
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Page 359
... Table 1 ( c ) as com- pared with Table 1 ( b ) , it is clear that the proportion of cross halogen product is increased by reduction of the rate of supply of hydrogen halide or by complete interruption of the supply . Direct Halogen ...
... Table 1 ( c ) as com- pared with Table 1 ( b ) , it is clear that the proportion of cross halogen product is increased by reduction of the rate of supply of hydrogen halide or by complete interruption of the supply . Direct Halogen ...
Page 564
... ( Table 4 ) . The magnetic susceptibilities of pure PuF , and pure PuO , have been measured recently ( Dawson , J. , 1952 , 1882 ) and this suggested an alternative means of analysing this reaction product , the magnetic susceptibility of ...
... ( Table 4 ) . The magnetic susceptibilities of pure PuF , and pure PuO , have been measured recently ( Dawson , J. , 1952 , 1882 ) and this suggested an alternative means of analysing this reaction product , the magnetic susceptibility of ...
Page 957
... Table 2 , coupled with those derived from Table 1 , reveal a trend which strongly suggests that the variable factor in these solvent grades is the water content . The effect of water on acetone solutions of potassium iodide has already ...
... Table 2 , coupled with those derived from Table 1 , reveal a trend which strongly suggests that the variable factor in these solvent grades is the water content . The effect of water on acetone solutions of potassium iodide has already ...
Contents
Organic | xv |
Magnetic Moments and Stereochemistry of Cobaltous Compounds | xv |
789Tetrahydro4 7sulphinylthionaphthen | 15 |
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absorption spectra acetic acid acetic anhydride acetone acetyl added addition alcohol alkaline alumina aluminium Amer amine ammonia aqueous atom band benzaldehyde benzene boiling bond bromide Calc carbonate carbonyl Chem chloride chloroform chromatography colour colourless complexes compound concentrated cooled crystallised crystals cyanogen cyanogen chloride decomp derivatives diazotised dilute dissolved distilled dried eluted equiv ester ether evaporated extracted ferric filtered formed Found fraction gave give H₂O heated hydrobromic acid hydrochloric acid hydrogen hydrogen chloride hydrolysis infra-red isolated ketone ligand light petroleum b. p. liquid m. p. and mixed methanol methyl mixed m. p. mixture molecule needles nitrate obtained orbitals oxidation phenol phosphate potassium hydroxide precipitate prepared pyridine reaction refluxed Reprint Order requires residue room temperature salt separated sodium carbonate sodium hydroxide solid solution solvent spectrum stirring sulphate sulphide sulphone sulphuric acid Table washed yield