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First Law of Thermodynamics
Energy is conserved: \Delta U = q + w
q in thermodynamics
Heat transferred into or out of a system.
w in thermodynamics
Work done on or by the system.
\Delta U
Change in internal energy of the system.
Formula for work by expansion/compression
w = -P \Delta V
Equation for heat transfer without a phase change
q = mc\Delta T
Enthalpy (H)
Heat content at constant pressure: H = U + PV
Calculation of \Delta H
\Delta H = \sum \Delta Hf^\circ(\text{products}) - \sum \Delta Hf^\circ(\text{reactants})
Entropy (S)
Measure of disorder; units = J/K or J/mol路K
How to calculate \Delta S
\Delta S = \sum S^\circ(\text{products}) - \sum S^\circ(\text{reactants})
Gibbs Free Energy formula
\Delta G = \Delta H - T\Delta S
Meaning of \Delta G < 0
The reaction is spontaneous.
Meaning of \Delta G = 0
The system is at equilibrium.
Relationship between \Delta G^\circ and K
\Delta G^\circ = -RT \ln K
Temperature unit in thermodynamics
Kelvin (K)
Formula for heat during a phase change
q = n \Delta H_{phase}
Difference between q at constant pressure vs. constant volume
qp = \Delta H; qv = \Delta U
Pressure-volume work to joules
1 \text{L路atm} = 101.3 \text{J}
Ideal gas law equation
PV = nRT
Equation relating Kp and Kc
Kp = Kc(RT)^{\Delta n}
R in J/mol路K
R = 8.314 \text{J/mol路K}
R in L路atm/mol路K
R = 0.0821 \text{L路atm/mol路K}
Meaning of positive \Delta S
More disorder or randomness in the system.
Hess鈥檚 Law
The total enthalpy change is the sum of individual steps.
Phase change occurrence
When temperature remains constant while heat is added or removed.
Standard \Delta H{vap} and \Delta H{fus} of water
\Delta H{vap} = 40.7 \text{kJ/mol}, \Delta H{fus} = 6.01 \text{kJ/mol}
Determine spontaneity from \Delta H and \Delta S
Use the spontaneity table with \Delta G = \Delta H - T\Delta S
Unit of heat capacity
J/g路K or J/mol路K
Sign of q if the system releases heat
q < 0
Sign of w when the system expands against a piston
w < 0