Quarterly Journal of the Chemical Society of London |
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Page 168
... give meso - radical adducts , e.g. 9 : 10 - dibenzyl - 9 : 10 - dihydroanthracene , in higher yields than meso ... give 9 - methyl - 10 - phenylanthracene , whereas methyl radicals give only 1 : 2 - di - 9 ' - anthrylethane.10 ...
... give meso - radical adducts , e.g. 9 : 10 - dibenzyl - 9 : 10 - dihydroanthracene , in higher yields than meso ... give 9 - methyl - 10 - phenylanthracene , whereas methyl radicals give only 1 : 2 - di - 9 ' - anthrylethane.10 ...
Page 378
... give alloinositol ( 65 mg . , 36 % ) , m . p . 310-320 ° ( decomp . ) . Dangschat and Fischer 11 record m . p . 270-275 ° . The inositol ( 35 mg . ) was heated with acetic anhydride ( 1 ml . ) and pyridine ( 1 ml . ) for 3 hr . at 100 ...
... give alloinositol ( 65 mg . , 36 % ) , m . p . 310-320 ° ( decomp . ) . Dangschat and Fischer 11 record m . p . 270-275 ° . The inositol ( 35 mg . ) was heated with acetic anhydride ( 1 ml . ) and pyridine ( 1 ml . ) for 3 hr . at 100 ...
Page 1233
... gives m . p . 101 ° , 84 % yield . • Stobbe , J. prakt . Chem . , 1929 , 123 , 241 ( NaOEt - EtOH ) , gives m . p . 94 ° , 45 % yield . Kostanecki and Tambor , Ber . , 1899 , 32 , 1924 ( NaOH ) , give m . p . 126 ° , yield not stated ...
... gives m . p . 101 ° , 84 % yield . • Stobbe , J. prakt . Chem . , 1929 , 123 , 241 ( NaOEt - EtOH ) , gives m . p . 94 ° , 45 % yield . Kostanecki and Tambor , Ber . , 1899 , 32 , 1924 ( NaOH ) , give m . p . 126 ° , yield not stated ...
Contents
19 | 4 |
The effect of temperature on azonitriles as initiators in the polymerization of styrene | 12 |
The kinetics and mechanisms of addition to olefinic substances Part V Products | 36 |
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absorption acetic acid acetic anhydride alcohol alkoxides Amer amine ammonia aniline anion aromatic atoms benzene boiling bromine buffer C₁ Calc carbonate catalysed cation Chem chloride chromatography colourless complex compound concentration constant containing crystallised decomp derivative diazotisation dilute dinitrogen trioxide disaccharide dissolved distilled equation ester ethanol ether ethylenediamine evaporated EXPERIMENTAL extracted filtered filtrate formation Found fraction gave give H₂O halides heated hydrochloric acid hydrogen hydrogen chloride hydrolysis hypochlorous iodide ionic isolated isomer K₁ kinetic ligand light petroleum b. p. m. p. and mixed mannose methyl mixed m. p. mixture mole mole-¹ molecular molecule needles niobium nitrate nitrosating nitrosonium nitrous acid obtained oxidation pentafluoride perchloric acid phenylhydrazine potassium precipitate prepared prisms pyridine rate-constants reaction reactivity refluxed requires residue resin salt silver sodium hydroxide solid solvent spectra stoicheiometric sugar sulphuric acid syrup Table values yellow yield