Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 1
... Compounds by Nitric Acid in Sulpholan and Nitro- methane By J. G. Hoggett , R. B. Moodie , and K. Schofield , * Department of Chemistry , University of Exeter The nitration in sulpholan , and to a lesser extent in nitromethane , of a ...
... Compounds by Nitric Acid in Sulpholan and Nitro- methane By J. G. Hoggett , R. B. Moodie , and K. Schofield , * Department of Chemistry , University of Exeter The nitration in sulpholan , and to a lesser extent in nitromethane , of a ...
Page 186
... compounds ( I ) , ( II ) , and ( III ) have already been reported 1 ] Relative intensity ( m / e 68 = 100 ) ... compounds ( I ) - ( V ) at an electron- beam energy of 70 ev are given in Table 2. It can be TABLE 2 Values of 1001 / ΣI for ...
... compounds ( I ) , ( II ) , and ( III ) have already been reported 1 ] Relative intensity ( m / e 68 = 100 ) ... compounds ( I ) - ( V ) at an electron- beam energy of 70 ev are given in Table 2. It can be TABLE 2 Values of 1001 / ΣI for ...
Page 504
... compounds ( I ) and ( III ) . Formation of the ions of m / e 66 and 79 to a significant extent in the spectra of compounds ( I ) and ( III ) indicates that the molecular ion of compound ( II ) is formed when com- pounds ( I ) and ( III ) ...
... compounds ( I ) and ( III ) . Formation of the ions of m / e 66 and 79 to a significant extent in the spectra of compounds ( I ) and ( III ) indicates that the molecular ion of compound ( II ) is formed when com- pounds ( I ) and ( III ) ...
Contents
Physical organic chemistry | 1 |
Aromatic reactivity Part XXXVIII Protodesilylation of 12dihydrobenzocyclobutene indan and tetralin | 12 |
Aromatic reactivity Part XL Additional substituent effects in protodetrimethylsilylation | 21 |
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absorption acetic acid Acta alcohol alkyl Amer amine angles anion aqueous aromatic ation benzene bond bromide calculated carbanion carbon tetrachloride CH₂ Chem chemical shifts Chemistry Chim chloride CO₂H compounds concentration conformation corresponding coupling constants decomposition derived di-imine dioxan dipole effect electron equation esters ethanol ether experimental Figure first-order formation formed H₂O hydrogen hydrolysis hydroxide hypochlorous acid interaction intermediate iodide irradiation isomer isomerisation isopropyl k₁ ketone kinetic measured mercuric mesitylene method methyl mixture mole mole-¹ molecular molecule n.m.r. spectra nitration nitrogen observed obtained olefin oxidation oxygen peaks peroxide phenyl Phys plot polymer proton radical rate constants ratio reactants reaction reactivity reduced relative resonance ring salts showed shown similar singlet sodium sodium hydroxide solution solvent solvolysis spectrum steric steric effect structure substituent sulphoxide t-butyl Table temperature titanium(III triethyl phosphite values