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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Page 1591
... methyl 3 - chlorobutyrate . The absence , even of traces , of methyl methacrylate was demonstrated ( g.l.c. ) . The gaseous products were shown ( by mass spectrographic analysis ) to contain methyl chloride as main component . Whilst ...
... methyl 3 - chlorobutyrate . The absence , even of traces , of methyl methacrylate was demonstrated ( g.l.c. ) . The gaseous products were shown ( by mass spectrographic analysis ) to contain methyl chloride as main component . Whilst ...
Page 1594
... Methyl crotonate , b . p . 120-5 ° , was prepared from crotonoyl chloride , methanol , and pyridine ( cf. Jeffery and Vogel 16 who record b . p . 119 ° / 768 mm . ) . Methyl isobutyrate , b . p . 90–91 ° , was prepared as described by ...
... Methyl crotonate , b . p . 120-5 ° , was prepared from crotonoyl chloride , methanol , and pyridine ( cf. Jeffery and Vogel 16 who record b . p . 119 ° / 768 mm . ) . Methyl isobutyrate , b . p . 90–91 ° , was prepared as described by ...
Page 1838
... methyl protons in compounds ( XIX ) , ( XX ) , and ( XXII ) , compared with methyl gibberellate ( 8-8 ) , are probably due to de - shielding by the oxygen function of the 2 - substituent ; they are not caused by the 2,3 - double bond ...
... methyl protons in compounds ( XIX ) , ( XX ) , and ( XXII ) , compared with methyl gibberellate ( 8-8 ) , are probably due to de - shielding by the oxygen function of the 2 - substituent ; they are not caused by the 2,3 - double bond ...
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