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The activation energy for the reaction is typically larger than the overall energy of the exergonic reaction (1). Endergonic reactions are nonspontaneous. The progress of the reaction is shown by the line. The change of Gibbs free energy (ΔG) during an endergonic reaction is a positive value because energy is gained (2).
The change of Gibbs free energy (ΔG) in an exergonic reaction (that takes place at constant pressure and temperature) is negative because energy is lost (2). In chemical thermodynamics, an exergonic reaction is a chemical reaction where the change in the free energy is negative (there is a net release of free energy). [1]
The entire reaction is usually catabolic. [13] The release of energy (called Gibbs free energy) is negative (i.e. −ΔG) because energy is released from the reactants to the products. An endergonic reaction is an anabolic chemical reaction that consumes energy. [3] It is the opposite of an exergonic reaction.
The reaction will only be allowed if the total entropy change of the universe is zero or positive. This is reflected in a negative ΔG, and the reaction is called an exergonic process. If two chemical reactions are coupled, then an otherwise endergonic reaction (one with positive ΔG) can be made to happen.
For exergonic and endergonic reactions, see the separate articles: Endergonic reaction; Exergonic reaction; See also. Exergonic process; Endergonic; Exothermic process;
An exergonic process is one which there is a positive flow of energy from the system to the surroundings. This is in contrast with an endergonic process. [ 1 ] Constant pressure, constant temperature reactions are exergonic if and only if the Gibbs free energy change is negative (∆ G < 0).
The chain of redox reactions driving the flow of electrons through the electron transport chain, from electron donors such as NADH to electron acceptors such as oxygen and hydrogen (protons), is an exergonic process – it releases energy, whereas the synthesis of ATP is an endergonic process, which requires an input of energy.
Figure 6:Reaction Coordinate Diagrams showing reactions with 0, 1 and 2 intermediates: The double-headed arrow shows the first, second and third step in each reaction coordinate diagram. In all three of these reactions the first step is the slow step because the activation energy from the reactants to the transition state is the highest.