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The degree of dissociation in gases is denoted by the symbol α, where α refers to the percentage of gas molecules which dissociate. Various relationships between K p and α exist depending on the stoichiometry of the equation. The example of dinitrogen tetroxide (N 2 O 4) dissociating to nitrogen dioxide (NO 2) will be taken.
The degree of dissociation is the fraction of the original solute molecules that have dissociated. It is usually indicated by the Greek symbol α {\displaystyle \alpha } . There is a simple relationship between this parameter and the van 't Hoff factor.
Thus, the degree of dissociation of a weak electrolyte is proportional to the inverse square root of the concentration, or the square root of the dilution. The concentration of any one ionic species is given by the root of the product of the dissociation constant and the concentration of the electrolyte.
Together with the formula above, the boiling-point elevation can be used to measure the degree of dissociation or the molar mass of the solute. This kind of measurement is called ebullioscopy ( Latin - Greek "boiling-viewing").
The degree of dissociation α (also known as degree of ionization), is a way of representing the strength of an acid. It is defined as the ratio of the number of ionized molecules and the number of molecules dissolved in water.
Stepwise dissociation constants are each defined for the loss of a single proton. The constant for dissociation of the first proton may be denoted as K a1 and the constants for dissociation of successive protons as K a2, etc. Phosphoric acid, H 3 PO 4, is an example of a polyprotic acid as it can lose three protons.
In chemistry, biochemistry, and pharmacology, a dissociation constant (K D) is a specific type of equilibrium constant that measures the propensity of a larger object to separate (dissociate) reversibly into smaller components, as when a complex falls apart into its component molecules, or when a salt splits up into its component ions.
α is the dissociation degree even for strong concentrated electrolytes, f λ is the lambda factor for concentrated solutions. This law is valid for low electrolyte concentrations only; it fits into the Debye–Hückel–Onsager equation. [6]