Quarterly Journal of the Chemical Society of London |
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Page 31
... gives arsonium salts more readily than its phenyl analogue ; e.g. , it unites vigorously with methyl iodide to give 2 : 2 - dimethylisoarsindolinium iodide . Furthermore , it also unites with o - xylylene dibromide to give 2-0 ...
... gives arsonium salts more readily than its phenyl analogue ; e.g. , it unites vigorously with methyl iodide to give 2 : 2 - dimethylisoarsindolinium iodide . Furthermore , it also unites with o - xylylene dibromide to give 2-0 ...
Page 497
... give 113 ° ) ; ( II ) 67 ° ( Nietzki , Annalen , 1882 , 215 , 125 , gives 67 ° ) ; ( III ) 38 ° ( prepared by the ... give 72 ° ) ; ( V ) 77 · 5 ° ( idem , ibid . , give 77 · 5 ° ) ; ( VI ) 83 ° ( idem , ibid . , give 83 ...
... give 113 ° ) ; ( II ) 67 ° ( Nietzki , Annalen , 1882 , 215 , 125 , gives 67 ° ) ; ( III ) 38 ° ( prepared by the ... give 72 ° ) ; ( V ) 77 · 5 ° ( idem , ibid . , give 77 · 5 ° ) ; ( VI ) 83 ° ( idem , ibid . , give 83 ...
Page 627
... give m . p . 161–162 ° corr . ) and thence into 5 - nitro - acetylanthranilic acid which formed pale yellow needles from water , m . p . 220 ° Ullmann and Úzbachian , Ber . , 1903 , 36 , 1797 , give m . p . 221 ° ) . Evaporation of the ...
... give m . p . 161–162 ° corr . ) and thence into 5 - nitro - acetylanthranilic acid which formed pale yellow needles from water , m . p . 220 ° Ullmann and Úzbachian , Ber . , 1903 , 36 , 1797 , give m . p . 221 ° ) . Evaporation of the ...
Contents
An Investigation of the Occurrence of the Coordinate or Dative Link by Electric Dipolemoment | 38 |
Electrolytic Dissociation Processes Part IV The Ionisation of a CarbonHalogen Bond | 129 |
By J SHERIDAN | 133 |
14 other sections not shown
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4-benzthiazine absorption acetic anhydride acetone acetyl acetylene added addition adsorbed alkali Amer ammonia aqueous atoms benzene boiling bond Calc carbinol carbon catalyst CH₂ Chem chloroform colourless needles compound concentrated condensation cooling crystallised from alcohol crystals cyclisation D.Sc decomp derivative described dilute dissolved distilled dried ester ethanol ether ethylene evaporated EXPERIMENTAL extracted filtered filtrate formation formed Found fraction gave give heated hydrocarbons hydrochloric acid hydrogen bromide hydrogen chloride hydrolysis iodide isolated ketone light petroleum liquid methiodide method methyl alcohol mixed m. p. mixture molecule nickel nitric nitrogen obtained optically oxide oxychloride phosphate phosphorus picrate potassium potassium hydroxide precipitate prepared pressure prisms pyridine reaction reduced refluxed requires residue ring room temperature salt saturated separated sodium carbonate sodium hydroxide solid soluble solution solvent structure substance sulphate sulphuric acid vacuum washed yellow needles yield zinc