Part of PC-04 — Chemical Thermodynamics

Glossary: Key Terms in Chemical Thermodynamics

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Adiabatic process: A process in which no heat exchange occurs between the system and surroundings (q=0q = 0). The system is perfectly insulated.

Bond dissociation enthalpy: Energy required to break 1 mole of a specific bond in gaseous molecules. Always positive (endothermic).

Cyclic process: A process where the system returns to its original state. All state function changes are zero (ΔU=ΔH=ΔS=ΔG=0\Delta U = \Delta H = \Delta S = \Delta G = 0).

Endothermic reaction: Reaction that absorbs heat from surroundings (ΔH>0\Delta H > 0).

Enthalpy (HH): Thermodynamic quantity H=U+PVH = U + PV. Change at constant pressure equals heat exchanged (ΔH=qp\Delta H = q_p).

Entropy (SS): Measure of disorder or randomness. ΔS=qrev/T\Delta S = q_{rev}/T. State function measured in J/(mol·K).

Exothermic reaction: Reaction that releases heat to surroundings (ΔH<0\Delta H < 0).

Free expansion: Expansion of gas into vacuum (Pext=0P_{ext} = 0). No work done (w=0w = 0).

Gibbs free energy (GG): G=HTSG = H - TS. Determines spontaneity at constant TT and PP. ΔG<0\Delta G < 0 for spontaneous processes.

Hess's Law: The enthalpy change of a reaction is path-independent (because HH is a state function).

Internal energy (UU): Total energy stored in a system (kinetic + potential energy of molecules). State function.

Isobaric process: Process at constant pressure. Heat exchanged equals ΔH\Delta H.

Isochoric process: Process at constant volume. No PV work done (w=0w = 0).

Isothermal process: Process at constant temperature. For ideal gases: ΔU=0\Delta U = 0, ΔH=0\Delta H = 0.

Path function: A quantity that depends on the path taken (not just initial and final states). Examples: heat (qq) and work (ww).

Reversible process: An idealized process conducted infinitesimally slowly such that the system is always in equilibrium. Gives maximum work.

Spontaneous process: A process that proceeds without continuous external assistance. Characterized by ΔG<0\Delta G < 0 at constant TT and PP.

Standard enthalpy of formation (ΔHf\Delta H_f^\circ): Enthalpy change when 1 mole of a compound is formed from its elements in standard states at 298 K, 1 bar.

Standard state: Pure substance at 1 bar and specified temperature (usually 298 K). ΔHf\Delta H_f^\circ of elements in standard state = 0.

State function: A property that depends only on the current state, not on how the state was reached. Examples: UU, HH, SS, GG, PP, VV, TT.

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