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What is the difference between exergonic and exothermic?

Published in Chemical Thermodynamics 4 mins read

The fundamental difference between exergonic and exothermic reactions lies in the type of energy they release and the thermodynamic criteria they satisfy: exothermic reactions release heat, while exergonic reactions release free energy, indicating spontaneity.

Understanding Exothermic Reactions

An exothermic reaction is a chemical process that releases energy in the form of heat to its surroundings. This release of heat causes the temperature of the surroundings to increase. In thermodynamic terms, an exothermic reaction is characterized by a negative change in enthalpy (ΔH < 0), meaning the enthalpy of the products is lower than that of the reactants.

  • Key Characteristic: Heat is given out to the surrounding.
  • Thermodynamic Sign: ΔH < 0 (negative enthalpy change).
  • Example: Burning wood, combustion of fuels, neutralization reactions.

Understanding Exergonic Reactions

An exergonic reaction is a chemical process that releases free energy to its surroundings. This release of free energy means the reaction can proceed spontaneously without continuous external energy input. In thermodynamics, an exergonic reaction is defined by a negative change in Gibbs free energy (ΔG < 0). Gibbs free energy accounts for both enthalpy and entropy changes within a system at a constant temperature.

  • Key Characteristic: Free energy is released, and the reaction is spontaneous.
  • Thermodynamic Sign: ΔG < 0 (negative Gibbs free energy change).
  • Example: Cellular respiration, dissolving of some salts in water (even if it makes the water cold).

Core Distinctions at a Glance

The table below highlights the key differences between these two important thermodynamic terms:

Feature Exothermic Reaction Exergonic Reaction
Energy Released Heat Free energy (usable energy for work)
Primary Measure Enthalpy (ΔH) Gibbs Free Energy (ΔG)
Sign of Change ΔH < 0 ΔG < 0
Indicates Heat release to surroundings Spontaneity of the reaction
Impact on Surrounding T Increases (releases heat) Can vary (depends on ΔH and TΔS components)
Relationship to Work Does not directly indicate ability to do work Indicates the maximum amount of non-expansion work that can be done
Example Burning of methane, freezing of water at 0°C ATP hydrolysis, cellular respiration, dissolving ammonium nitrate (spontaneous but endothermic)

The Relationship Between Exergonic and Exothermic

It's crucial to understand that while many exothermic reactions are also exergonic, and vice-versa, they are not interchangeable terms.

  • Exothermic does not always mean Exergonic: A reaction can release heat (ΔH < 0) but still be non-spontaneous (ΔG > 0) if the decrease in entropy (disorder, ΔS) is significant and the temperature is low. For instance, freezing water at temperatures above 0°C is exothermic (releases heat) but non-spontaneous (endergonic).
  • Exergonic does not always mean Exothermic: A reaction can be spontaneous (ΔG < 0) even if it absorbs heat from the surroundings (endothermic, ΔH > 0). This happens when there is a significant increase in entropy (ΔS > 0) that outweighs the endothermic enthalpy change, especially at higher temperatures. A classic example is the dissolving of ammonium nitrate in water, which feels cold (endothermic) but occurs spontaneously (exergonic).

The relationship is governed by the Gibbs Free Energy equation:

ΔG = ΔH - TΔS

Where:

  • ΔG is the change in Gibbs free energy
  • ΔH is the change in enthalpy
  • T is the absolute temperature (in Kelvin)
  • ΔS is the change in entropy

For a reaction to be exergonic (spontaneous, ΔG < 0), the total free energy must decrease. This can happen in several ways:

  1. ΔH is negative (exothermic) and ΔS is positive (increasing disorder): Always exergonic.
  2. ΔH is negative (exothermic) and ΔS is negative (decreasing disorder): Exergonic if the magnitude of ΔH is greater than the magnitude of TΔS.
  3. ΔH is positive (endothermic) and ΔS is positive (increasing disorder): Exergonic if the magnitude of TΔS is greater than the magnitude of ΔH.

Practical Implications

Understanding the difference between exergonic and exothermic processes is fundamental in various scientific fields:

  • Chemistry: Predicting reaction feasibility and designing synthetic pathways.
  • Biology: Explaining metabolic pathways where energy is captured and utilized (e.g., ATP hydrolysis, which is highly exergonic, powering many cellular processes).
  • Engineering: Designing efficient energy systems and chemical reactors.

By distinguishing between heat release and the release of usable free energy, scientists can better predict and control chemical and biological processes.