W1 Thermochem Flashcards
(13 cards)
1st law of thermodynamics in equations
ΔU = q + w
= ΔH - pΔV (at constant pressure)
q = heat of system = ΔH (at constant pressure)
w = work done on system = -pΔV (gases at constant pressure)
Work done by gases equation
what does it mean if its negative/positive
w = pΔV
negative -> expansion
positive -> compression
U
Internal energy
Sum of kinetic and potential energy of all particles in a system
Utotal = Ukinetic + Upotential
∆H
Function related to the heat absorbed or evolved by a chemical system - heat at constant volume (qsystem= ∆H)
Gibbs Free energy
Energy available to do work
∆G = ∆H - T∆S
Standard enthalpy of reaction
ΔrHθ
value of ΔH for a reaction occuring under standard conditions (105 Pa, 298K)
involves moles specified by question
Enthalpy of formation
∆fHɵ
energy required to form one mol of a substance from its elemental parts under standard conditions (105 Pa, 298K)
Entropy of surroundings equation
∆Ssurroundings = qsurroundings/T
2nd law of thermodynamics
For a spontaneous reaction: ΔStotal > 0
Definition of entropy
S = k lnW
K is Botlzmann’s constant, W is the number of microstates that the energy of a system can be distributed
Factors that affect entropy
Higher entropy caused by:
- Higher volume
- Higher temperature
- State: Gas > water > solid
- Higher no. particles
Gibbs free energy related to K
Under equilibrium conditions, ∆rG is zero so: ∆Gθ= - R T InK
