Thermodynamics
50 lessons, pages 1716–1765.
- What Thermodynamics Describes — Energy changes, states and the limits of thermodynamic prediction
- System, Surroundings and Boundary — Defining the matter and energy included in a calculation
- Open, Closed and Isolated Systems — Classifying matter and energy exchange across a boundary
- State Functions and Path Functions — Why internal energy is state-dependent while heat and work depend on a route
- Heat and Work Sign Conventions — Tracking energy entering and leaving a chemical system
- Internal Energy and the First Law — Applying ΔU = q + w to a defined system
- Pressure-Volume Work — Using w = −PextΔV for expansion against constant external pressure
- Reversible Isothermal Gas Work — Integrating ideal-gas pressure for a quasistatic isothermal path
- Free Expansion and Path Dependence — Contrasting zero external-pressure work with other paths
- Ideal-Gas Internal Energy and Temperature — Relating ΔU to temperature change for an ideal gas
- Enthalpy as U + PV — Defining a state function useful for constant-pressure processes
- Heat at Constant Pressure and Volume — Conditions under which qp = ΔH and qv = ΔU
- Connecting Reaction ΔH and ΔU — Using gas-mole change for ideal-gas reactions
- Heat Capacity and Temperature Change — Relating supplied heat to a measured temperature rise
- Specific, Molar and Total Heat Capacity — Selecting mass, mole and sample-based heat-capacity units
- Calorimetry and Heat Balance — Equating heat lost and gained in an insulated measurement
- Bomb Calorimetry — Measuring combustion heat at approximately constant volume
- Coffee-Cup Calorimetry — Inferring solution-reaction enthalpy at near-constant pressure
- Thermochemical Equations — Scaling enthalpy with stoichiometric reaction extent
- Exothermic and Endothermic Profiles — Reading reaction-energy diagrams and ΔH signs
- Standard States and Standard Enthalpy — Reference pressure, pure substances and temperature reporting
- Standard Enthalpy of Formation — Forming one mole of compound from elements in standard states
- Reaction Enthalpy from Formation Data — Products-minus-reactants calculation with stoichiometric coefficients
- Enthalpy of Combustion — Complete oxidation of one mole of a stated fuel
- Enthalpy of Neutralisation — Acid-base heat and the common strong-acid strong-base net reaction
- Enthalpy of Solution and Dilution — Separating dissolution and subsequent concentration changes
- Enthalpy of Phase Changes — Fusion, vaporisation and sublimation as state-dependent energy changes
- Enthalpy of Atomisation — Producing gaseous atoms from an element in its reference state
- Bond Dissociation Enthalpy — Homolytic breaking of a specified gas-phase bond
- Average Bond Enthalpy Estimates — Broken-minus-formed bond sums and their approximation limits
- Hess's Law — Using state-function path independence to sum reaction enthalpies
- Reversing and Scaling Thermochemical Equations — Adjusting ΔH correctly when equations are manipulated
- Hess Calculations from Formation Reactions — Building target equations from standard formation steps
- Thermochemical Cycles — Constructing a closed enthalpy route with a known target
- Lattice Enthalpy Conventions — Distinguishing crystal formation from lattice dissociation signs
- Born-Haber Cycle Steps — Atomisation, ionisation, electron gain and crystal formation
- Calculating a Salt's Lattice Enthalpy — Solving a sodium-chloride Born-Haber energy balance
- Entropy and Energy Dispersal — Interpreting accessible arrangements without equating entropy to disorder
- Microstates and Boltzmann Entropy — Connecting multiplicity to S = kB ln Ω
- Standard Molar Entropy — Reading tabulated absolute entropy values and units
- Reaction Entropy from Standard Data — Products-minus-reactants calculation for ΔrS°
- Entropy Change of the Surroundings — Using −ΔHsys/T for an isothermal constant-pressure reservoir
- Second Law and Total Entropy — Testing spontaneous direction through system plus surroundings
- Gibbs Energy and Spontaneity — Applying ΔG = ΔH − TΔS at constant temperature and pressure
- Temperature Thresholds for ΔG — Finding when opposing enthalpy and entropy terms change sign
- Gibbs Energy Away from Standard Conditions — Using ΔG = ΔG° + RT ln Q for reaction direction
- Gibbs Energy and Equilibrium Constant — Interpreting ΔG° = −RT ln K without equating it to ΔG at equilibrium
- Coupled Processes and Feasibility — Summing Gibbs energy changes for linked reactions
- Mixed Thermodynamics Problems — Choosing heat, work, enthalpy or Gibbs methods from stated conditions
- Thermodynamics: Unit Review — Integrating the first law, Hess cycles, entropy and Gibbs energy