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AP® Physics 2: Algebra-Based · Unit 9 · Topic 9.6

Entropy and the Second Law of Thermodynamics: Revision Notes (Physics 2 9.6)

One-page recap of entropy as spreading energy, the second law for isolated systems, entropy as a state function, equilibrium and closed systems.

Short on time? This page is the recap. For explanations, Figures 1 and 2 and the worked examples, use the full study guide.

Recap

  • Entropy S describes how spread out a system’s energy is. Spread-out energy means high entropy and less energy available to do work.
  • Concentrated energy spreads out by itself: hot spots even out, gases fill their containers, moving objects stop.
  • Second law: the total entropy of an isolated system never decreases. It is constant only if every process is reversible.
  • Real processes (friction, mixing, free expansion, heating across a temperature difference) are irreversible and raise total entropy.
  • An isolated system moves spontaneously toward thermodynamic equilibrium, where its entropy is at its maximum.
  • Only qualitative reasoning is needed. You never calculate entropy in this course.

Key relationships

Situation Entropy statement Why
Isolated system, real process ΔS_total > 0 irreversible
Isolated system, ideal reversible process ΔS_total = 0 reversible limit
Isolated system at equilibrium S at maximum; no further change nothing left to spread
Closed system cooled (energy leaves by heating) ΔS_system can be < 0 surroundings gain at least as much S
Closed system heated (energy enters by heating) ΔS_system > 0 energy spreads into it
System completes a cycle ΔS_system = 0 state function
Two paths, same end states same ΔS_system state function; Q and W differ

Assumptions behind the statements

  • “Isolated” means no energy and no matter cross the boundary. Check the boundary before you apply the second law.
  • “Closed” means energy can cross but matter cannot.
  • Reversible processes are idealised: very slow, no friction, no heating across a finite temperature difference.

Mistakes to avoid

  1. Applying “entropy never decreases” to a closed system. It applies to the total for an isolated system.
  2. Thinking the second law breaks energy conservation. Energy is always conserved; the second law sets the direction.
  3. Saying ΔS depends on the path. The system’s ΔS does not; only Q, W and the surroundings’ changes do.
  4. “Q = 0, so ΔS = 0.” A free expansion has Q = 0 but ΔS_gas > 0.
  5. “Cold to hot is impossible.” It is impossible only spontaneously. A freezer does it using work.
  6. Calling every slow process reversible. It also needs no friction and no heating across a temperature difference.

Quick self-check

  1. Hot soup cools in a room. What happens to the entropy of the soup, the room and the total? (Soup decreases; room increases by more; total increases.)
  2. A gas completes a cycle. What is ΔS for the gas? (Zero: entropy is a state function.)
  3. A gas is heated with 400 J and does 400 J of work while expanding at constant temperature. What is ΔU? Does its entropy rise or fall? (ΔU = 0; its entropy rises because it spreads into a larger volume.)
  4. When is the total entropy of an isolated system constant? (Only if every process is reversible.)

Next: practice questions.

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