Chapter 10 - Spontaneous Change Flashcards
Entropy (S), microscopic
S = klnΩ
S: entropy
k: Boltzmann constant, 1.38066e-23 J/K = R/Na
ln: natural log
Ω: number of microstates (omega)
Describes entropy on a microscopic level
Entropy (S), macroscopic
∆S = qrev/T
qrev: q reversible (because q isn’t a state function)
∆G < 0
Spontaneous
∆G > 0
Non-spontaneous
∆G = 0
Equilibrium
What is ∆G equal to (no K)?
∆G = ∆H - T∆S
∆G: Gibbs free energy
∆H: enthalpy
∆S: change in entropy
Can add ° and it’s the same
∆G for Q
∆G = ∆G° + RTlnQ
∆G°: ∆G of formation, ∆G standard
R: 8.3145 J/molK (might need to convert to kJ)
ln: natural log
Q: reaction quotient
∆G° for K
∆G° = -RTlnK
R: 8.3145 J/molK
ln: natural log
K: equilibrium constant
Calculate change in entropy of surroundings
∆Ssurr = -∆Hsys/T
∆Ssurr: change in entropy of surroundings
∆Hsys: change in enthalpy of system
T: temperature in K
When ∆Suniv is > 0, is the reaction product-favored or reactant-favored?
Product-favored
When ∆Suniv is < 0, is the reaction product-favored or reactant-favored?
Reactant-favored
How is the enthalpy term affected when ∆H° is greater or less than 0?
∆H° < 0, enthalpy is favorable
∆H° > 0, enthalpy is unfavorable
How is the entropy term affected by ∆S° is greater or less than 0?
∆S° < 0, entropy is unfavorable
∆S° > 0, entropy is favorable