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If a dynamic equilibrium is disturbed by changing the conditions, the position of equilibrium moves to partially reverse the change. For example, adding more S (to the chemical reaction above) from the outside will cause an excess of products, and the system will try to counteract this by increasing the reverse reaction and pushing the ...
In chemistry, Le Chatelier's principle (pronounced UK: / l ə ʃ æ ˈ t ɛ l j eɪ / or US: / ˈ ʃ ɑː t əl j eɪ /) [1] is a principle used to predict the effect of a change in conditions on chemical equilibrium. [2] Other names include Chatelier's principle, Braun–Le Chatelier principle, Le Chatelier–Braun principle or the equilibrium ...
Chemical equilibrium is a dynamic state in which forward and backward reactions proceed at such rates that the macroscopic composition of the mixture is constant. Thus, equilibrium sign ⇌ symbolizes the fact that reactions occur in both forward ⇀ {\displaystyle \rightharpoonup } and backward ↽ {\displaystyle \leftharpoondown } directions.
The Van 't Hoff equation relates the change in the equilibrium constant, K eq, of a chemical reaction to the change in temperature, T, given the standard enthalpy change, Δ r H ⊖, for the process. The subscript r {\displaystyle r} means "reaction" and the superscript ⊖ {\displaystyle \ominus } means "standard".
At equilibrium, the chemical force driving the forward reaction must be equal to the chemical force driving the reverse reaction. Writing the initial active masses of A,B, A' and B' as p, q, p' and q' and the dissociated active mass at equilibrium as ξ {\displaystyle \xi } , this equality is represented by
In chemistry, transition state theory (TST) explains the reaction rates of elementary chemical reactions. The theory assumes a special type of chemical equilibrium (quasi-equilibrium) between reactants and activated transition state complexes. [1] TST is used primarily to understand qualitatively how chemical reactions take place.
Under pure thermodynamic reaction control, when the equilibrium has been reached, the product distribution will be a function of the stabilities G°. After an infinite amount of reaction time, the ratio of product concentrations will equal the equilibrium constant K eq and therefore be a function of the difference in Gibbs free energies,
The extent of reaction is a useful quantity in computations with equilibrium reactions. [citation needed] Consider the reaction 2 A ⇌ B + 3 C. where the initial amounts are = , = , = , and the equilibrium amount of A is 0.5 mol. We can calculate the extent of reaction in equilibrium from its definition