Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 23
... Ether Formation from Diarylmethylenes and Alcohols By D. Bethell , * A. R. Newall , and D. Whittaker , The Robert Robinson Laboratories , University of Liverpool , P.O. Box 147 , Liverpool L69 3BX The thermal decomposition of ...
... Ether Formation from Diarylmethylenes and Alcohols By D. Bethell , * A. R. Newall , and D. Whittaker , The Robert Robinson Laboratories , University of Liverpool , P.O. Box 147 , Liverpool L69 3BX The thermal decomposition of ...
Page 798
... ether ( II ) the intensity of the new absorption was of similar intensity to that of the initial ( II ) , while for reaction of ( I ) it was about a factor of 10 lower than that of the initial ( I ) . This suggests that the final ...
... ether ( II ) the intensity of the new absorption was of similar intensity to that of the initial ( II ) , while for reaction of ( I ) it was about a factor of 10 lower than that of the initial ( I ) . This suggests that the final ...
Page 1251
... ether . We consider that this partial control of stereochemistry is incompatible with it being entirely controlled ... ether ( 11 ) Bornyl methyl ether ( 12 ) cis - 2 - Methylpinanyl ether ( 13 ) trans - 2 - Methyl pinanyl ether ( 14 ) a ...
... ether . We consider that this partial control of stereochemistry is incompatible with it being entirely controlled ... ether ( 11 ) Bornyl methyl ether ( 12 ) cis - 2 - Methylpinanyl ether ( 13 ) trans - 2 - Methyl pinanyl ether ( 14 ) a ...
Contents
Physical organic chemistry | 1 |
Contents | 6 |
Kinetics and mechanism of electrophilic substitution of heteroaromatic compounds Part XXIV Acid | 11 |
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A2 mechanism acetic acid-catalysed addition alcohol alkaline hydrolysis Amer analysis anion aqueous aromatic benzene benzoate bond bromine cal mol-1 calculated carbon atom carbonium ion carbonyl catalysis Chem Chemistry chlorine compounds concentration conjugate conjugate acid correlation deuterium diastereomers dienamines dioxan electron pairs energy entropies of activation epoxide equation esters ether ethylene exchange experimental Figure formation glycol H₂O hydrogen hydroxide hypochlorous acid indicate intramolecular isomer isotope effects k₁ k₂ ketone kinetic MeOH methanol methanolysis methiodide method methyl mixture mmHg mol-¹ molecular molecule n-pentyl n.m.r. spectra nitration nucleophilic observed obtained olefin oxidation oxygen p-xylene parameters perchloric acid Phys polar positive proton R. J. W. Le Fèvre radical rate coefficients rate constants ratio reaction constant reactivity relative resorcinol ring sodium solution solvent steric steric effects structure studied substituent substituted substrate t-butyl Table temperature Tetrahedron thiophen trans triethylborane values