Journal of the Chemical SocietyThe Society., 1949 |
From inside the book
Results 1-3 of 59
Page 904
... aniline in benzene solution is smaller than the true moment determined as a gas . Such a conclusion would be contrary to the opinions of a number of authors already cited ( e.g. , Cowley and Partington , Higasi , etc. ) who have ...
... aniline in benzene solution is smaller than the true moment determined as a gas . Such a conclusion would be contrary to the opinions of a number of authors already cited ( e.g. , Cowley and Partington , Higasi , etc. ) who have ...
Page 1151
... aniline in the presence of a trace of hydrogen chloride at 250 ° and 2500-3000 atm . to give a polymeric product consisting of aniline residues linked by methylene and / or carbinol groups in the o- and p - positions . The probable ...
... aniline in the presence of a trace of hydrogen chloride at 250 ° and 2500-3000 atm . to give a polymeric product consisting of aniline residues linked by methylene and / or carbinol groups in the o- and p - positions . The probable ...
Page 1152
... anilines was consistent with this interpretation . Dimethyl- aniline failed to react with carbon monoxide under the conditions used for aniline , and methylaniline gave only N - methylformanilide . Primary amines having one substituent ...
... anilines was consistent with this interpretation . Dimethyl- aniline failed to react with carbon monoxide under the conditions used for aniline , and methylaniline gave only N - methylformanilide . Primary amines having one substituent ...
Other editions - View all
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 bromine Calc carbon catalyst CH₂ Chem chloroform citrinin colourless needles compound condensation containing 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