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Entropy and Gibbs Free
Energy
Chemistry
Mr. Hamza Suharwardi
Spontaneous Process
 A process that occurs without outside
intervention/involvement.
 Spontaneous processes can be fast or
slow!
What Factors Determine the
Spontaneity of a Reaction?
Entropy
Enthalpy
 What ties the two together is:
Gibbs Free Energy.
Entropy
 Symbol S
 A measure of molecular randomness or
disorder.
Disorder
 Chemical processes
spontaneously go to a direction
of increased entropy.
 Why?
 Probability
Probability of Disorder
 Is there a higher probability your room
will be messy or neat as time goes on?
System
the part of the universe under investigation.
Entropy of the System
 Is greater in:
 Gases than solids.
 Larger volumes of gases than smaller volumes.
 Larger number of gas molecules than smaller
number of gas molecules.
Example:
 Which has more entropy in its system?
H2O (s) or H2O (g)
Enthalpy (Heat of Reaction)
 Enthalpy (H) is the sum of the internal
energy and pressure times volume.
We cannot measure the enthalpy of a
system, but we can look at changes in
enthalpy. H = E + P V.
 Spontaneity is favored when the process is
exothermic (DH<0).
 An exothermic process releases heat,
causing the temperature of the immediate
surroundings to rise. An endothermic
process absorbs heat and cools the
surroundings.”
Example of a spontaneous exothermic
reaction:
 2SO2(g)+ O2(g) 2SO3(g) + heat
 DH<0
So…… :
 When
DH <0 and DSsystem>0
(exothermic) (Greater Disorder)
the reaction would be spontaneous.
 Are all spontaneous reactions
exothermic and with a greater
system disorder?
 Answer: No.
What about exothermic and less
disorder? Use Gibbs Free Energy
 Gibbs Free Energy can be used to predict
the spontaneity and it ties together the
DH and the DS, the two driving forces of
reactions.
DG= DH-TDS
 (all quantities refer to the system)
Gibbs Free Energy
 Energy that can be converted to work.
 DG<0 for spontaneous processes.
 DG=0 at equilibrium.
Thanks!
Any questions?
You can find me at
● @hamzaahmed
● hamzaahmed0696@mail.me

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Entropy and Gibbs Free Energy.ppt

  • 1. Entropy and Gibbs Free Energy Chemistry Mr. Hamza Suharwardi
  • 2. Spontaneous Process  A process that occurs without outside intervention/involvement.  Spontaneous processes can be fast or slow!
  • 3. What Factors Determine the Spontaneity of a Reaction? Entropy Enthalpy  What ties the two together is: Gibbs Free Energy.
  • 4. Entropy  Symbol S  A measure of molecular randomness or disorder.
  • 5. Disorder  Chemical processes spontaneously go to a direction of increased entropy.  Why?  Probability
  • 6. Probability of Disorder  Is there a higher probability your room will be messy or neat as time goes on?
  • 7. System the part of the universe under investigation.
  • 8. Entropy of the System  Is greater in:  Gases than solids.  Larger volumes of gases than smaller volumes.  Larger number of gas molecules than smaller number of gas molecules.
  • 9. Example:  Which has more entropy in its system? H2O (s) or H2O (g)
  • 10. Enthalpy (Heat of Reaction)  Enthalpy (H) is the sum of the internal energy and pressure times volume. We cannot measure the enthalpy of a system, but we can look at changes in enthalpy. H = E + P V.  Spontaneity is favored when the process is exothermic (DH<0).  An exothermic process releases heat, causing the temperature of the immediate surroundings to rise. An endothermic process absorbs heat and cools the surroundings.”
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  • 15. Example of a spontaneous exothermic reaction:  2SO2(g)+ O2(g) 2SO3(g) + heat  DH<0
  • 16. So…… :  When DH <0 and DSsystem>0 (exothermic) (Greater Disorder) the reaction would be spontaneous.
  • 17.  Are all spontaneous reactions exothermic and with a greater system disorder?  Answer: No.
  • 18. What about exothermic and less disorder? Use Gibbs Free Energy  Gibbs Free Energy can be used to predict the spontaneity and it ties together the DH and the DS, the two driving forces of reactions. DG= DH-TDS  (all quantities refer to the system)
  • 19. Gibbs Free Energy  Energy that can be converted to work.  DG<0 for spontaneous processes.  DG=0 at equilibrium.
  • 20. Thanks! Any questions? You can find me at ● @hamzaahmed ● hamzaahmed0696@mail.me