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. |
From inside the book
Results 1-3 of 78
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 ...
Other editions - View all
Common terms and phrases
1-methylheptyl 1-phenylethyl bromide absorption acetic acid acetone acetonitrile adducts alcohol alginic acid Amer amine anhydride aniline aqueous atom benzene bond Calc calculated carbon Chem chloride chloroform CHPh chromatography cm.¹ complex compounds concentration crystallised cyanohydrin derivative diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether evaporated EXPERIMENTAL extracted formation formed Found fraction gave H₂O halides hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum isomers k₁ k₂ kcal ketone kinetic ligand magnesium manganese(III methanolysis methyl mixed m. p. mixture mmoles mole mole-¹ molecule nitrogen nucleophilic o-complex obtained optical oxaloacetic acid oxidation peaks peroxide petroleum b. p. phenols phosphate phosphine picryl potassium prepared proton pyridine rate coefficients reaction reflux requires residue room temperature rotation shown silanes sodium solution solvent spectra structure substituted sulphide sulphuric Table tetracyanoethylene titration tricyanovinyl values yield