Thermodynamics Flashcards
Potential energy and kinetic energy
Kinetic: energy associated with motion
- can be measured
Potential: stored energy
- can not be measured directly
Enthalpy
The heat absorbed or released during a process
Exothermic: energy released (delta H -)
Endothermic: energy absorbed (delta H +)
See notes
Spontaneous and nonspontaneous process
First law of thermodynamics: conservation of energy
- energy can be converted between different types, but cannot be created or destroyed
Spontaneity process is based on the difference in energy between the final and initial states
- spontaneous if direction toward equilibrium and total energy goes down
- if spontaneous in one direction then nonspont the other
Entropy
- a mixture of the randomness or degrees of freedom
- phase affects entropy
- number of particles affects entropy
- temperature affects entropy: increasing S increases T
See notes for increasing and decreasing entropy
Entropy: 2nd Law of Thermodynamics
- in any spontaneous process
DeltaSuniverse=deltasystem+deltasurroundings > 0 J/K*mol
Entropy: 3rd Law of Thermodynamics
- S=0 J/K*mol
Gibbs Free Energy
- G=H-TS
- negDeltaG is spont and exergonic
- posDeltaG is nonspont and endergonic
- zero DeltaG = 0 and equilibrium
Spontaneity on Gibbs
- spont at high T: (?)=(+)-(+)(+)
- spont at low T: (?)=(-)-(+)(-)
- spont (-)=(-)-(+)(+)
- nonspont (+)=(+)-(+)(-)
Gibbs Free Energy definition
- the total free energy is theoretical
- max amt of work that can be done bye the system (spont)
- max amt of work required to be done on the system (nonspont)
Calculating G
Grxn=EGproducts-EGreactants
Grxn=-RTln(K)
Standard Cell Potential= Grxn=-nFEcell
K=e^(-Grxn/RT)
- nonstandard conditions calls for balancing the rxns by reversing or multiplying and adding H2O, H+, and electrons