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Free energy is made up of an enthalpy term and an entropy term. [11] = The standard enthalpy change can be determined by calorimetry or by using the van 't Hoff equation, though the calorimetric method is preferable. When both the standard enthalpy change and acid dissociation constant have been determined, the standard entropy change is easily ...
This quantity with the dimension of time is useful because it is independent of concentration. The quantity 1/k, also with dimension of time, equal to the half life divided by 0.6932, is known as the residence time or time constant. [77] The residence time for water exchange varies from about 10 −10 s for Cs + to about 10 +10 s (more than 200 ...
The following are strong acids in aqueous and dimethyl sulfoxide solution. As mentioned above, because the dissociation is so strongly favored, the concentrations of and thus the values of cannot be measured experimentally. The values in the following table are average values from as many as 8 different theoretical calculations.
In its path, a PKA can produce effects similar to those of heating and rapidly quenching a metal, resulting in Frenkel defects. A thermal spike does not last long enough to permit annealing of the Frenkel defects. [1] [2] A different model called the displacement spike was proposed for fast neutron bombardment of heavy elements.
The higher the proton affinity, the stronger the base and the weaker the conjugate acid in the gas phase.The (reportedly) strongest known base is the ortho-diethynylbenzene dianion (E pa = 1843 kJ/mol), [3] followed by the methanide anion (E pa = 1743 kJ/mol) and the hydride ion (E pa = 1675 kJ/mol), [4] making methane the weakest proton acid [5] in the gas phase, followed by dihydrogen.
The self-ionization of water (also autoionization of water, autoprotolysis of water, autodissociation of water, or simply dissociation of water) is an ionization reaction in pure water or in an aqueous solution, in which a water molecule, H 2 O, deprotonates (loses the nucleus of one of its hydrogen atoms) to become a hydroxide ion, OH −.
The free energy change, dG r, can be expressed as a weighted sum of change in amount times the chemical potential, the partial molar free energy of the species. The chemical potential, μ i , of the i th species in a chemical reaction is the partial derivative of the free energy with respect to the number of moles of that species, N i
The Debye–Hückel theory was proposed by Peter Debye and Erich Hückel as a theoretical explanation for departures from ideality in solutions of electrolytes and plasmas. [1] It is a linearized Poisson–Boltzmann model, which assumes an extremely simplified model of electrolyte solution but nevertheless gave accurate predictions of mean activity coefficients for ions in dilute solution.