Journal of the Chemical Society, Part 2, Pages 1201-2488The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Results 1-3 of 41
Page 1217
... Peroxide and Benzoyl Peroxide . By H. B. HENBEST , J. A. W. REID , and C. J. M. STIRLING . Decomposition of t - butyl peroxide in t - butyl methyl ether at 140 ° yielded a mixture of compounds in which neopentyl alcohol was identified ...
... Peroxide and Benzoyl Peroxide . By H. B. HENBEST , J. A. W. REID , and C. J. M. STIRLING . Decomposition of t - butyl peroxide in t - butyl methyl ether at 140 ° yielded a mixture of compounds in which neopentyl alcohol was identified ...
Page 1220
... Peroxide and Benzoyl Peroxide . By H. B. HENBEST , J. A. W. REID , and C. J. M. STIRLING . Thioanisole and t - butyl peroxide at 140 ° give 1,2 - di ( phenylthio ) ethane and nuclear methylated products . By contrast , photochemical ...
... Peroxide and Benzoyl Peroxide . By H. B. HENBEST , J. A. W. REID , and C. J. M. STIRLING . Thioanisole and t - butyl peroxide at 140 ° give 1,2 - di ( phenylthio ) ethane and nuclear methylated products . By contrast , photochemical ...
Page 1223
... peroxide ( 7 · 05 g . , 0 · 1 mole ) were irradiated in a quartz flask for 80 hr . at 40-45 ° with a Hanovia mercury ... peroxide ( 78 % ) . Removal of the excess of thioanisole , and chromatography of the residue on alumina in light ...
... peroxide ( 7 · 05 g . , 0 · 1 mole ) were irradiated in a quartz flask for 80 hr . at 40-45 ° with a Hanovia mercury ... peroxide ( 78 % ) . Removal of the excess of thioanisole , and chromatography of the residue on alumina in light ...
Contents
NO PAGE | 1205 |
The SN mechanism in aromatic compounds Part XXX The sydnone ring | 1213 |
NO PAGE | 1224 |
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1-phenylethyl absorption acetic acid acetone acetonitrile adducts alcohol alginic acid Amer amine aniline aqueous atom benzene bond bromide Calc calculated carbon carboxyl CH₂ Chem chloride chloroform chromatography cm.¹ complex compounds concentration corresponding crystallised derived diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether evaporated experimental extracted fluorine formation formed Found fraction gave H₂O hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum iodide ionisation isomers k₁ k₂ kcal kinetic ligand methanolysis methyl mixed m. p. mixture mmoles mole mole-¹ molecule nitrogen nucleophilic o-complex obtained optical orbitals oxaloacetic acid oxidation oxygen peaks peroxide phenols phosphate phosphine potassium prepared proton pyridine rate coefficients reaction reduced reflux requires residue room temperature rotation shown similar sodium solution solvent spectra structure substituted sulphide sulphuric t-butyl Table tetracyanoethylene titration tricyanovinyl values yield