Journal of the Chemical Society, Part 2, Pages 1201-2488The Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
From inside the book
Results 1-3 of 82
Page 1344
... nucleophilic step ( the " carbon basicity " ) . 1,26 This is not readily measurable in nucleophilic attacks of this type , as the carbanions first formed enter into various types of rapid reactions . However , the existence of such an ...
... nucleophilic step ( the " carbon basicity " ) . 1,26 This is not readily measurable in nucleophilic attacks of this type , as the carbanions first formed enter into various types of rapid reactions . However , the existence of such an ...
Page 1360
... nucleophilic reactions on carbon - carbon double bonds . IN nucleophilic reactions on carbon - carbon double bonds the initially formed carbanion or zwitterion may enter a variety of different pathways , resulting in addition ...
... nucleophilic reactions on carbon - carbon double bonds . IN nucleophilic reactions on carbon - carbon double bonds the initially formed carbanion or zwitterion may enter a variety of different pathways , resulting in addition ...
Page 1366
... nucleophilic attack . Comparison of the positive values with those for other nucleophilic attcks on double bonds shows them to be higher than that for the barbiturate anion - ẞ - nitrostyrene system ( p : 0-74 ) , 26 but comparable to ...
... nucleophilic attack . Comparison of the positive values with those for other nucleophilic attcks on double bonds shows them to be higher than that for the barbiturate anion - ẞ - nitrostyrene system ( p : 0-74 ) , 26 but comparable to ...
Contents
NO PAGE | 1205 |
The SN mechanism in aromatic compounds Part XXX The sydnone ring | 1213 |
NO PAGE | 1224 |
57 other sections not shown
Other editions - View all
Common terms and phrases
1-phenylethyl absorption acetic acid acetone acetonitrile adducts alcohol alginic acid Amer amine aniline aqueous atom benzene bond bromide Calc calculated carbon carboxyl CH₂ Chem chloride chloroform chromatography cm.¹ complex compounds concentration corresponding crystallised derived diazomethane diphenylphosphinic dissociation constants distilled enol equation equilibrium constants ester ethanol ether evaporated experimental extracted fluorine formation formed Found fraction gave H₂O hydrazine hydrides hydrogen cyanide hydrolysis hydroxide infrared spectrum iodide ionisation isomers k₁ k₂ kcal kinetic ligand methanolysis methyl mixed m. p. mixture mmoles mole mole-¹ molecule nitrogen nucleophilic o-complex obtained optical orbitals oxaloacetic acid oxidation oxygen peaks peroxide phenols phosphate phosphine potassium prepared proton pyridine rate coefficients reaction reduced reflux requires residue room temperature rotation shown similar sodium solution solvent spectra structure substituted sulphide sulphuric t-butyl Table tetracyanoethylene titration tricyanovinyl values yield