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  • Wiley-Blackwell  (2)
  • 2015-2019
  • 1985-1989  (2)
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Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 2 (1989), S. 507-518 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The hydrolysis reactions of N-(2,4,6-trinitrophenyl)piperidine (2) and N-(2,4,6-trinitrophenyl)-morpholine (3) were studied. Two kinetic processes well separated in time are observed in both reactions. The fastest process, which is reversible, leads to the formation of a species of λmax 260 and 410 nm and is attributed to the formation of a σ complex of stoichiometry 1 : 2 due to the addition of a second HO- to the σ complex of 1 : 1 stoichiometry. The slowest process leads quantitatively to picrate ion. The equilibrium constants for the formation of the σ complexes of 1:1 and 1:2 stoichiometries and the rate of formation and decomposition of the latter complex were determined. The kinetic data for the slow process lead to the conclusion that the picrate ion is formed from the attack of HO- on the two σ complexes, confirming previous findings. There are some differences in the calculated rates for 2 and 3 which may be an indication that the elimination of the amine is partially rate determining.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 17 (1985), S. 859-869 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The addition of water to 1-(4-Z-2,6-dinitrophenyl)-3-methylimidazolium chloride (Z = CN, NO2, and CF3) is catalyzed by carboxylate bases. There is a decrease in ρ with increasing basicity of the catalyst with ∂ρ/∂pKBH = -0.090. The results indicate that the mechanism of the reaction involves the addition of water to the aromatic substrates catalyzed by general bases. The changes in the structure-reactivity parameters with changing pK of the catalysts or Z in the substrate are rationalized in terms of changing bond lengths in the transition state. The activation parameters and the kinetic solvent isotopic effect were determined for the water, acetate, and OH- catalyzed reactions and are consistent with the proposed mechanism.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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