| 1 | Celsius in Carnot | η = 1 − 27/127 = 78.7% | Carnot formula requires absolute temperature (kelvin) | Always convert: T(K) = T(°C) + 273. η = 1 − 300/400 = 25% |
| 2 | Adiabatic = isothermal | Conclude T is constant in adiabatic because Q = 0 | Q = 0 means no heat exchange, not no temperature change | In adiabatic: ΔU = −W. Expansion → W > 0 → ΔU < 0 → T decreases |
| 3 | Wrong sign for W | W = nRT ln(V1/V2) instead of ln(V2/V1) | Inverted logarithm ratio | W = nRT ln(V2/V1). Expansion (V2 > V1): W > 0. Compression: W < 0. |
| 4 | ΔU ≠ 0 for isothermal | Write ΔU = nCᵥΔT even for isothermal | For ideal gas, U depends only on T. If T constant, ΔU = 0 | ΔU = 0 for isothermal process of ideal gas regardless of formula used |
| 5 | Forgetting γ in adiabatic | Use PV = const instead of PV^γ = const | Adiabatic ≠ isothermal. Extra γ from the coupled ΔU term | Adiabatic: PV^γ = const. Isothermal: PV = const. γ > 1 always. |
| 6 | v_mp > v_rms | Reverse the speed order | Confusion about "most probable" vs "maximum" | Always: v_mp < v_avg < v_rms. RMS is largest because v2 weighting elevates it. |
| 7 | C_p = C_v for any gas | Assume C_p = C_v | Extra work done at constant pressure requires extra heat | C_p − C_v = R (Mayer's relation). C_p > C_v always for any ideal gas. |
| 8 | Wrong γ for gas type | Use γ = 5/3 for diatomic gas | Monoatomic: f = 3, γ = 5/3. Diatomic: f = 5, γ = 7/5 = 1.4 | Identify gas type first. Monoatomic: He, Ar. Diatomic: O2, N2, H2. |
| 9 | Treating polyatomic as diatomic | Use f = 5 for CO2 | CO2 is polyatomic (nonlinear): f = 6, γ = 4/3 | Check molecular type. CO2, H2O, NH3: f = 6 (3 trans + 3 rot). |