Journal of the Chemical SocietyThe Society., 1963 |
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Page 175
... give mesityl oxide Amax . 235 mμ ( ɛ 14,000 ) and crotonaldehyde 217 mu ( both in EtOH ) . 5 Nagakura , Minegishi , and Stanfield ( J. Amer . Chem . Soc . , 1957 , 79 , 1033 ) give mesityl oxide Amax . 284 mu ( ≈ 15,600 ) ( in H2SO1 ) ...
... give mesityl oxide Amax . 235 mμ ( ɛ 14,000 ) and crotonaldehyde 217 mu ( both in EtOH ) . 5 Nagakura , Minegishi , and Stanfield ( J. Amer . Chem . Soc . , 1957 , 79 , 1033 ) give mesityl oxide Amax . 284 mu ( ≈ 15,600 ) ( in H2SO1 ) ...
Page 505
... give colourless needles of 4 - chloro - 2 - methyl - 6- ( methylthio ) benzamide ( 17.2 g . ) , m . p . 200-202 ° ( Found : C , 50.5 ; H , 4.9 ; Cl , 16 · 7 ; N , 6 · 4 ; S , 14.9 . C , H10CINOS requires C , 50-1 ; H , 4 · 6 ; Cl , 16 ...
... give colourless needles of 4 - chloro - 2 - methyl - 6- ( methylthio ) benzamide ( 17.2 g . ) , m . p . 200-202 ° ( Found : C , 50.5 ; H , 4.9 ; Cl , 16 · 7 ; N , 6 · 4 ; S , 14.9 . C , H10CINOS requires C , 50-1 ; H , 4 · 6 ; Cl , 16 ...
Page 1222
... give metal and nitrate ions only , and the unusual behaviour of beryllium nitrate is attributed to the strength of the metal - oxygen bond . Strong covalent bonding of the nitrate group occurs in the alkyl nitrates , and the ...
... give metal and nitrate ions only , and the unusual behaviour of beryllium nitrate is attributed to the strength of the metal - oxygen bond . Strong covalent bonding of the nitrate group occurs in the alkyl nitrates , and the ...
Contents
M W and Herbich M A | 1 |
NO PAGE | 15 |
The reaction of titanium halides with tertiary amines | 33 |
134 other sections not shown
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absorption acetic acid acetic anhydride acetone acetyl alcohol alkyl alumina Amer anhydride anion aqueous atom band benzene bond bromide Calc carbon carbonyl cation CH₂ Chem chloride chromatography cm.¹ colourless complexes compound concentration constants crystallised crystals cyclic decomp decomposition derivatives diethyl dilute dioxan distilled diynes dried effect electron eluted ester ethanol ether ethyl acetate evaporated extracted formed Found fraction gave give heated hydrochloric acid hydrogen hydrogen chloride hydrolysis infrared infrared spectrum iodide isomer isotope K₁ ketone light petroleum liquid m. p. and mixed methyl mixed m. p. mixture mole molecule needles nitrogen nuclear magnetic resonance obtained oxide oxygen perchlorate phenol picrate potassium prepared proton pyridine reaction reduced refluxed requires residue ring room temperature sample sodium hydroxide solid solution solvent spectra structure substituted Table tetrahydrofuran triethylamine ultraviolet values yellow yield