Journal of the Chemical SocietyThe Society., 1949 |
From inside the book
Results 1-3 of 83
Page 817
... reaction of dibenzyl hydrogen phosphate with cyclohexene oxide ; the further development of this phosphorylation method in the preparation of sugar phosphates using anhydro - sugars as intermediates has also been studied and will form ...
... reaction of dibenzyl hydrogen phosphate with cyclohexene oxide ; the further development of this phosphorylation method in the preparation of sugar phosphates using anhydro - sugars as intermediates has also been studied and will form ...
Page 1146
... reaction between RX and AgNO , in aqueous ethyl alcohol proceeds substantially according to eqn . ( 2 ) , or that such side reactions as may occur have a similar overall molar heat of reaction to ( 2 ) . Studies of the reactions between ...
... reaction between RX and AgNO , in aqueous ethyl alcohol proceeds substantially according to eqn . ( 2 ) , or that such side reactions as may occur have a similar overall molar heat of reaction to ( 2 ) . Studies of the reactions between ...
Page 1214
... reaction mixture , the time ( t ) for a given fraction of the oxidation to occur was determined . The apparent order of the reaction was then calculated from the formula n = 1+ ( log t1 / ta ) / log ( a2 / a1 ) , where t1 and t2 are the ...
... reaction mixture , the time ( t ) for a given fraction of the oxidation to occur was determined . The apparent order of the reaction was then calculated from the formula n = 1+ ( log t1 / ta ) / log ( a2 / a1 ) , where t1 and t2 are the ...
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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 bromine Calc carbon catalyst CHâ‚‚ 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