Journal of the Chemical Society, Part 1The Society., 1959 |
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Page 316
... soluble and fairly soluble signify solubility of about † 0 = Nil ; = cooling ; + = slight ; ++ = considerable . Formation of solvates in acetyl chloride has been known since 1901 when a solvate of aluminium chloride was reported.8 ...
... soluble and fairly soluble signify solubility of about † 0 = Nil ; = cooling ; + = slight ; ++ = considerable . Formation of solvates in acetyl chloride has been known since 1901 when a solvate of aluminium chloride was reported.8 ...
Page 318
... soluble in acetyl chloride give highly conducting solutions . These also increase the chloride - ion concentration and will act as ansolvobases . The behaviour of these compounds as acids or bases is confirmed in Parts III and IV of ...
... soluble in acetyl chloride give highly conducting solutions . These also increase the chloride - ion concentration and will act as ansolvobases . The behaviour of these compounds as acids or bases is confirmed in Parts III and IV of ...
Page 448
... soluble products . When the nitrate was treated in methyl cyanide solution with benzylamine or morpholine , the yield of water - soluble nitrite was practically quantitative . Fluorenone was isolated from the ether - soluble products of ...
... soluble products . When the nitrate was treated in methyl cyanide solution with benzylamine or morpholine , the yield of water - soluble nitrite was practically quantitative . Fluorenone was isolated from the ether - soluble products of ...
Contents
3Dioxa and 1 3 | 1 |
Triterpenoids Part LVII The oxidation of norfriedelanone with selenium dioxide | 38 |
2dichloro3 4epoxybutane and related compounds | 44 |
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Common terms and phrases
absorption acetic acid acetone acetyl chloride added alcohol alkaline alumina Amer amine anhydride aqueous sodium atom band benzene boiling bond bromide Calc carbonyl CH₂ Chem chloroform chromatography complex compound concentrated cooled crystallised cyclohexene decomp derivative dilute dioxan distilled dried electron eluted epoxide ester ethanol evaporated excess extracted with ether filtered filtrate fluoride formation formed Found fraction gave give heated under reflux hydrochloric acid hydrogen chloride hydrolysis hydroxyl ibid infrared spectrum iodide isolated isomers ketone lithium aluminium hydride m. p. and mixed methyl mixed m. p. mixture mmole molecule needles nitrate nitrogen nitrous acid obtained olefin oxidation oxygen peroxide picrate potassium hydroxide precipitate prepared pyridine radicals reaction reagent reduced requires residue room temperature salt separated sodium hydroxide solid solution solvent spectra structure sulphuric acid Table tetrachloride triethylamine ultraviolet values washed yellow yield