Journal of the Chemical Society, Part 2Chemical Society., 1949 |
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Results 1-3 of 83
Page 1291
... Chem . Soc . , 1933 , 55 , 3624. ( 2 ) Gold- schmidt and Salcher , Z. physikal . Chem . , 1899 , 29 , 89. ( 3 ) Hahn and Klockmann , ibid . , 1904 , 48 , 435 . ( 4 ) Lunden , J. Chim . physique , 1907 , 5 , 574. ( 5 ) Mizutani , Z ...
... Chem . Soc . , 1933 , 55 , 3624. ( 2 ) Gold- schmidt and Salcher , Z. physikal . Chem . , 1899 , 29 , 89. ( 3 ) Hahn and Klockmann , ibid . , 1904 , 48 , 435 . ( 4 ) Lunden , J. Chim . physique , 1907 , 5 , 574. ( 5 ) Mizutani , Z ...
Page 1368
... Chem . Soc . , 1947 , 69 , 303 ) . This was unexpected in view of the behaviour of the closely related 4 - hydroxyquinazoline ( Bogert and Geiger , J. Amer . Chem . Soc . , 1912 , 34 , 524 ; Morley and Simpson , J. , 1948 , 360 ) and 4 ...
... Chem . Soc . , 1947 , 69 , 303 ) . This was unexpected in view of the behaviour of the closely related 4 - hydroxyquinazoline ( Bogert and Geiger , J. Amer . Chem . Soc . , 1912 , 34 , 524 ; Morley and Simpson , J. , 1948 , 360 ) and 4 ...
Page 1465
... Chem . , 1892 , 9 , 553 ) if , in the form m . p . 35 ° , the phenyl and the hydroxyl were not vicinal . The difficulty has since been cleared by conductivity observations directly on the two oximes themselves in liquid sulphur dioxide ...
... Chem . , 1892 , 9 , 553 ) if , in the form m . p . 35 ° , the phenyl and the hydroxyl were not vicinal . The difficulty has since been cleared by conductivity observations directly on the two oximes themselves in liquid sulphur dioxide ...
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Common terms and phrases
4-dinitrophenylhydrazone absorption acetic anhydride acetone acetyl acidified added aldehyde alkaline aluminium chloride Amer amine ammonia aniline aqueous sodium atom benzene boiling bond bromine Calc carbon catalyst CH₂ Chem chloroform citrinin colourless needles compound condensation cooled crystallised crystallised from alcohol crystals cyanide cyclisation decomp derivative dilute dissolved distilled dried electrode ester evaporated extracted with ether filtered filtrate formed colourless Found fraction gave give heated under reflux hydrochloric acid hydrogen chloride hydrolysis iodide isolated ketone lactone light petroleum b. p. m. p. and mixed methanol method methyl alcohol minutes mixed m. p. mixture molecule obtained oxide phenol phosphoric picrate potassium hydroxide precipitate prepared pyridine reaction reduced pressure requires residue resin room temperature salt separated sodium hydroxide solid soluble solution solvent specimen structure substance sulphuric acid triethylamine values washed yellow needles yield