Zero-order reaction is a reaction for which the rate of reaction is independent of the concentration of reactants.
Reversible reaction is a chemical reaction that can proceed in both the forward and backward directions. When reversible reactions reach equilibrium the forward and reverse reactions are still happening but at the same rate, so the concentrations of reactants and products do not change. A reversible reaction is denoted by a double arrow pointing both directions in a chemical equation.
The equilibrium constant (K) was originally introduced in 1863 by Norwegian chemists C.M. Guldberg and P. Waage using the law of mass action. For a reversible chemical reaction represented by the equation
chemical equilibrium occurs when the rate of the forward reaction equals the rate of the back reaction, so that the concentrations of products and reactants reach steady-state values.
The equilibrium constant is the ratio of chemical activities of the species A, B, C, and D at equilibrium.
To a certain approximation, the activities can be replaced by concentrations.
For gas reactions, partial pressures are used rather than concentrations
The units of Kp and Kc depend on the numbers of molecules appearing in the stoichiometric equation (a, b, c, and d).
The value equilibrium constant depends on the temperature. If the forward reaction is exothermic, the equilibrium constant decreases as the temperature rises. The equilibrium constant shows the position of equilibrium. A low value of K indicates that [C] and [D] are small compared to [A] and [B]; i.e. that the back reaction predominates.
The equilibrium constant is related to ΔrG°, the standard Gibbs free energy change in the reaction, by
A point-like object that undergoes circular motion changes its angular position from initial Θi to final Θf, relative to a fixed axis, specified in a coordinate system with an origin that coincides the centre of the circular path of object. The change in its angular position is called angular displacement ΔΘ = Θf - Θi. Also, a rigid body that rotates about a specified rotation axis, changing its angular position from initial Θi to final Θf, undergoes an angular displacement ΔΘ.
The average angular velocity, ωav, is the ratio of the angular displacement and the time interval Δt=tf-ti, in which that displacement occurs.
Θf and Θi are the initial and final angular position, respectively.
The instantaneous angular velocity ω is the limit of the average angular velocity, as Δt is made to approach zero.
ωav and ω are positive for the counterclockwise rotation (in direction of increasing Θ) and negative for the clockwise rotation (in direction of decreasing Θ).
SI unit for angular velocity is s-1.The measure for the angle Θ is radian. The relationship between radians and degrees is:
For example, the angular velocity of the minute hand of a clock is:
Endothermic reactions are the ones in which heat is absorbed and are facilitated by an increase in temperature (ΔH° > 0).
If the reaction is endothermal in one direction, in the opposite direction the reaction is exothermal.
Faradaic reaction is a heterogeneous charge-transfer reaction occurring at the surface of an electrode.
Forward reaction is a reaction in which products are produced from reactants and it goes from left to right in a reversible reaction.
Heterogenic reactions are those reactions which take place in different phases (in different aggregate states).
Homogenic reactions are those reactions in which products and reactants are in the same phase (aggregate state).
Mannich reaction is a process in which hydrogen atoms in organic compounds are replaced with a methyl group.
Generalic, Eni. "Jednadžba brzine reakcije." Croatian-English Chemistry Dictionary & Glossary. 29 June 2022. KTF-Split. {Date of access}. <https://glossary.periodni.com>.
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