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	<title>Gibbs Free Energy - Revision history</title>
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		<title>Thakshashila: Created page with &quot;== Gibbs Free Energy ==  &#039;&#039;&#039;Gibbs Free Energy&#039;&#039;&#039; (denoted as &lt;math&gt;G&lt;/math&gt;) is a thermodynamic potential that measures the maximum reversible work a thermodynamic system can perform at constant temperature and pressure. It is an important concept in chemistry and physics, used to predict the spontaneity of chemical reactions and phase changes.  === Definition === Gibbs Free Energy is defined as:  &lt;math&gt;G = H - TS&lt;/math&gt;  where:   * &lt;math&gt;G&lt;/math&gt; = Gibbs free energy   *...&quot;</title>
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		<updated>2025-06-12T11:47:35Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Gibbs Free Energy ==  &amp;#039;&amp;#039;&amp;#039;Gibbs Free Energy&amp;#039;&amp;#039;&amp;#039; (denoted as &amp;lt;math&amp;gt;G&amp;lt;/math&amp;gt;) is a thermodynamic potential that measures the maximum reversible work a thermodynamic system can perform at constant temperature and pressure. It is an important concept in chemistry and physics, used to predict the spontaneity of chemical reactions and phase changes.  === Definition === Gibbs Free Energy is defined as:  &amp;lt;math&amp;gt;G = H - TS&amp;lt;/math&amp;gt;  where:   * &amp;lt;math&amp;gt;G&amp;lt;/math&amp;gt; = Gibbs free energy   *...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Gibbs Free Energy ==&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Gibbs Free Energy&amp;#039;&amp;#039;&amp;#039; (denoted as &amp;lt;math&amp;gt;G&amp;lt;/math&amp;gt;) is a thermodynamic potential that measures the maximum reversible work a thermodynamic system can perform at constant temperature and pressure. It is an important concept in chemistry and physics, used to predict the spontaneity of chemical reactions and phase changes.&lt;br /&gt;
&lt;br /&gt;
=== Definition ===&lt;br /&gt;
Gibbs Free Energy is defined as:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;math&amp;gt;G = H - TS&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
where:  &lt;br /&gt;
* &amp;lt;math&amp;gt;G&amp;lt;/math&amp;gt; = Gibbs free energy  &lt;br /&gt;
* &amp;lt;math&amp;gt;H&amp;lt;/math&amp;gt; = enthalpy of the system  &lt;br /&gt;
* &amp;lt;math&amp;gt;T&amp;lt;/math&amp;gt; = absolute temperature (in Kelvin)  &lt;br /&gt;
* &amp;lt;math&amp;gt;S&amp;lt;/math&amp;gt; = entropy of the system&lt;br /&gt;
&lt;br /&gt;
=== Physical Significance ===&lt;br /&gt;
* A negative change in Gibbs free energy (&amp;lt;math&amp;gt;\displaystyle \Delta G &amp;lt; 0&amp;lt;/math&amp;gt;) indicates a spontaneous process.  &lt;br /&gt;
* If &amp;lt;math&amp;gt;\displaystyle \Delta G = 0&amp;lt;/math&amp;gt;, the system is in equilibrium.  &lt;br /&gt;
* If &amp;lt;math&amp;gt;\displaystyle \Delta G &amp;gt; 0&amp;lt;/math&amp;gt;, the process is non-spontaneous and requires energy input.&lt;br /&gt;
&lt;br /&gt;
=== Relation to Chemical Reactions ===&lt;br /&gt;
For a chemical reaction at constant temperature and pressure, the change in Gibbs free energy is given by:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;math&amp;gt;\Delta G = \Delta H - T \Delta S&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
where &amp;lt;math&amp;gt;\Delta H&amp;lt;/math&amp;gt; is the change in enthalpy and &amp;lt;math&amp;gt;\Delta S&amp;lt;/math&amp;gt; is the change in entropy during the reaction.&lt;br /&gt;
&lt;br /&gt;
The sign and magnitude of &amp;lt;math&amp;gt;\Delta G&amp;lt;/math&amp;gt; determine whether a reaction proceeds spontaneously:&lt;br /&gt;
&lt;br /&gt;
* Exergonic reactions: &amp;lt;math&amp;gt;\Delta G &amp;lt; 0&amp;lt;/math&amp;gt;, reaction releases free energy and is spontaneous.  &lt;br /&gt;
* Endergonic reactions: &amp;lt;math&amp;gt;\Delta G &amp;gt; 0&amp;lt;/math&amp;gt;, reaction absorbs free energy and is non-spontaneous.&lt;br /&gt;
&lt;br /&gt;
=== Gibbs Free Energy and Equilibrium Constant ===&lt;br /&gt;
The standard Gibbs free energy change (&amp;lt;math&amp;gt;\Delta G^\circ&amp;lt;/math&amp;gt;) is related to the equilibrium constant &amp;lt;math&amp;gt;K&amp;lt;/math&amp;gt; of a reaction by:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;math&amp;gt;\Delta G^\circ = -RT \ln K&amp;lt;/math&amp;gt;&lt;br /&gt;
&lt;br /&gt;
where:  &lt;br /&gt;
* &amp;lt;math&amp;gt;R&amp;lt;/math&amp;gt; is the universal gas constant  &lt;br /&gt;
* &amp;lt;math&amp;gt;T&amp;lt;/math&amp;gt; is the temperature in Kelvin  &lt;br /&gt;
* &amp;lt;math&amp;gt;K&amp;lt;/math&amp;gt; is the equilibrium constant&lt;br /&gt;
&lt;br /&gt;
This relation allows prediction of the position of equilibrium and the spontaneity of the reaction.&lt;br /&gt;
&lt;br /&gt;
=== Applications ===&lt;br /&gt;
* Predicting spontaneity of chemical reactions  &lt;br /&gt;
* Calculating equilibrium constants  &lt;br /&gt;
* Understanding biological processes such as ATP hydrolysis  &lt;br /&gt;
* Designing industrial chemical processes&lt;br /&gt;
&lt;br /&gt;
=== References ===&lt;br /&gt;
* Atkins, P., &amp;amp; de Paula, J. (2010). &amp;#039;&amp;#039;Physical Chemistry&amp;#039;&amp;#039;. Oxford University Press.  &lt;br /&gt;
* Laidler, K. J. (1996). &amp;#039;&amp;#039;Chemical Kinetics&amp;#039;&amp;#039;. Harper &amp;amp; Row.&lt;br /&gt;
&lt;br /&gt;
[[Category:Chemistry]]&lt;/div&gt;</summary>
		<author><name>Thakshashila</name></author>
	</entry>
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