Quarterly Journal of the Chemical Society of London |
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Page 2852
... formed in aprotic solvents , i.e. , in solvents other than ethanol . * Under acid catalysis , which , according to our evidence , is of the specific hydrogen - ion type , involving the preliminary and complete transfer of one proton to ...
... formed in aprotic solvents , i.e. , in solvents other than ethanol . * Under acid catalysis , which , according to our evidence , is of the specific hydrogen - ion type , involving the preliminary and complete transfer of one proton to ...
Page 3151
... formed during the irradiation of a mixture of 18 mm . of methyl nitrite and 300 mm . of nitric oxide . There was no thermal reaction following the irradiation . If the product is nitrogen dioxide , the quantum yield , estimated ...
... formed during the irradiation of a mixture of 18 mm . of methyl nitrite and 300 mm . of nitric oxide . There was no thermal reaction following the irradiation . If the product is nitrogen dioxide , the quantum yield , estimated ...
Page 3697
... formed from a protonated precursor , or formed in a protonation reaction . In any event , an essential step would seem to involve reaction between acetyl nitrate and acid . Acetoxylating entities which might be formed from acetyl ...
... formed from a protonated precursor , or formed in a protonation reaction . In any event , an essential step would seem to involve reaction between acetyl nitrate and acid . Acetoxylating entities which might be formed from acetyl ...
Contents
NO PAGE | 2842 |
Mechanism of benzidine and semidine rearrangements Part XV A collective | 2864 |
By DAVID PETERS | 2901 |
Copyright | |
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absorption acetic acid acetone added adduct alcohol alkyl Amax Amer anhydride aqueous aromatic atom atomic orbitals band benzene bond bromine Calc carbon carbonyl cation CH₂ Chem chloroform chromatography cm.¹ complex compound concentration constant crystallised cyclohexane decomp decomposition derivatives dilute dimethyl distilled dried effect electron ester ethanol ether evaporated extracted filtered filtrate formation formed Found fraction gave give heated hydride hydrogen hydrolysis hydroxide infrared infrared spectrum iodide ionisation energies isomer kinetic light petroleum b. p. lithium lithium aluminium hydride mechanism methyl mixed m. p. mixture mole molecular molecule nitric oxide nitrogen Nujol observed obtained oxidation perchlorate phenyl potassium prepared proton pyridine reaction rearrangement reduced refluxed requires residue room temperature salt sodium sodium hydroxide solid solution solvent spectra steric steric effect structure substitution sulphate Table thionyl chloride transition ultraviolet values Vmax yield