Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 41
... Yield + Yield t ( R.C. ) ( H2O ) Yield † Yield † Dose * ( R.C. ) ( H2O2 ) Dose * Yield + Yield † ( R.C. ) ( H2O2 ) Dose * Yield † Yield † Yield † Yield t ( R.C. ) ( H2O2 ) Dose * ( R.C. ) ( H2O2 ) ( a ) In Oxygen 0.86 1.7 2.5 0.86 1.9 ...
... Yield + Yield t ( R.C. ) ( H2O ) Yield † Yield † Dose * ( R.C. ) ( H2O2 ) Dose * Yield + Yield † ( R.C. ) ( H2O2 ) Dose * Yield † Yield † Yield † Yield t ( R.C. ) ( H2O2 ) Dose * ( R.C. ) ( H2O2 ) ( a ) In Oxygen 0.86 1.7 2.5 0.86 1.9 ...
Page 427
... yield of anisole after 18 hr . is far greater when Perkadox ( di - isopropyl peroxydicarbonate ) is included ( cf. experiments 15 and 18 ) ; this compound , TABLE 8 Decomposition of p - anisyl - lead triacetate in acetic acid or [ 2H1 ] ...
... yield of anisole after 18 hr . is far greater when Perkadox ( di - isopropyl peroxydicarbonate ) is included ( cf. experiments 15 and 18 ) ; this compound , TABLE 8 Decomposition of p - anisyl - lead triacetate in acetic acid or [ 2H1 ] ...
Page 467
... yield values suggest a comparatively higher rate for spin pairing followed by fast radical recombin- ation to ( V ) . Despite a low overall quantum yield , the photostability of fulvene ( VI ) allows a high conversion . The difference ...
... yield values suggest a comparatively higher rate for spin pairing followed by fast radical recombin- ation to ( V ) . Despite a low overall quantum yield , the photostability of fulvene ( VI ) allows a high conversion . The difference ...
Contents
Physical organic chemistry | 1 |
Topochemistry Part XXX Crystal and molecular structures of chalcone | 11 |
Conformational studies Part I Crystal and molecular structures of cis12dipchlorobenzoyl and cis | 17 |
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A. R. Katritzky alcohol alkyl Amer anion aqueous aromatic ation axial benzene bond bromination calculated carbanion carbon acids carbon atom carbon tetrachloride carbonyl catalyst Chem chemical shifts Chemistry chloride complex compounds concentration conformation correlation coupling constants crystal cyclohexane derivatives difference dilute dimethyl sulphoxide dioxan electron elimination energy equation equatorial equilibrium ester ethanol ether experimental Figure fluorene formation fraction H₂O H₂SO hydrogen hydrolysis hydroxide indicators interaction intermediate ionisation isomer isomerization isotope effect k₁ k₂ kcal kcal./mole kinetic measured mechanism methyl mixture mole mole-¹ molecular molecule n.m.r. spectra nitration nitrogen nucleophilic observed obtained oxide oxime oxygen parameters phenyl Phys piperidine plot proton pyridines R. P. Bell radical rate constants ratio reaction reactivity ring shown shows sodium solution solvent spectrum structure substituents sulphuric acid t-butyl Table temperature Tetrahedron thiophen transition values