Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Khawla Al-Mallah"'
Autor:
Khawla Al-Mallah, Geoffrey Stedman
Publikováno v:
Journal of Chemical Research. :670-671
The kinetic profile of the rate constant for the nitrous acid–amide reaction in sulfuric acid as a function of acidity for a range of aliphatic and aromatic primary amides has been interpreted in terms of the HNO2/NO+ and the amide/amide·H+ equili
Publikováno v:
The Journal of Organic Chemistry. 52:1710-1713
Des substituants electroattracteurs sont necessaires a la transposition, en position ortho ou para par rapport a la fonction N-O. L'ordre de reactivite dans cette transposition est NO 2 >>CN>COPh>COMe>COOEt>CONH 2 . Mecanisme cyclique intramoleculair
Publikováno v:
ChemInform. 19
Publikováno v:
ChemInform. 18
Publikováno v:
Chemischer Informationsdienst. 17
Rates (k) of isomerization of (Ia) correlate with the H-bonding ability of protic solvents such as (II) or THF - H2O mixtures.
Publikováno v:
ChemInform. 18
Publikováno v:
Chemischer Informationsdienst. 6
Thiourea reacts rapidly with nitrous acid in aqueous solution to form an equilibrium concentration of a coloured S-nitroso-compound. The equilibrium constant has been measured, together with a preliminary value of the rate constant for the nitrosatio
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :413
The rate of rearrangement of N-arylamine oxides (4) to O-arylhydroxylamines (5) was measured in different solvents. The rate of isomerisation of p-nitrophenyl N-oxides correlates with the dielectric constants of aprotic solvents and with the hydrogen
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :2469
Thiourea reacts rapidly with nitrous acid in aqueous solution to form an equilibrium concentration of a coloured S-nitroso-compound. The equilibrium constant has been measured, together with a preliminary value of the rate constant for the nitrosatio
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :109
The N-oxides of N-(2,4-dinitrophenyl)-piperidines and -morpholine undergo thermal rearrangement to the substituted hydroxylamines. The kinetics of the rearrangement were studied in aprotic solvents at four or five temperatures. Steric and polar facto