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Internal Energy: First Law, Work, and Heat

Internal energy (U) is a state function representing the total energy of a system. The first law of thermodynamics states ΔU = q + w: energy change equals heat transferred plus work done. For ideal gases, U depends only on temperature: ΔU = nCvΔT.

Concept Fundamentals
ΔU = q + w
First Law
w = -PΔV
Work
ΔU = nCvΔT
Ideal gas
Path independent
State fn
Internal Energy CalculatorCompute ΔU from heat, work, or ideal gas parameters

Why This Chemistry Calculation Matters

Why: Internal energy is fundamental to thermodynamics. The first law governs energy conservation. State functions like U are path-independent; heat and work are not. Understanding ΔU is essential for process analysis and calorimetry.

How: Use ΔU = q + w when heat and work are known. For ideal gases, ΔU = nCvΔT (Cv = 3R/2 monatomic, 5R/2 diatomic). Work at constant pressure: w = -PΔV. Sign convention: q > 0 heat in; w > 0 work on system.

  • Internal energy is a state function—depends only on current state, not path.
  • For ideal gases, isothermal processes have ΔU = 0 (U depends only on T).
  • Adiabatic: q = 0, so ΔU = w; isochoric: w = 0, so ΔU = q.

Sample Examples

Calculation Mode

Process Type

Units

Heat added to system (positive) or removed (negative)
Work done on system (positive) or by system (negative)
Number of significant figures for results

⚠️For educational and informational purposes only. Verify with a qualified professional.

🔬 Chemistry Facts

📐

First law: ΔU = q + w (energy conservation).

— IUPAC

⚖️

Work by system at constant P: w = -PΔV.

— NIST

💨

Ideal gas: ΔU = nCvΔT; U independent of P and V.

— Kinetic theory

🌡️

Isothermal ideal gas: ΔU = 0, so q = -w.

— Thermodynamics

📋 Key Takeaways

  • ΔU = q + w | First law: internal energy change from heat and work
  • ΔU = nCvΔT | Ideal gas: U depends only on temperature
  • w = -PΔV | Work at constant pressure
  • Isothermal: ΔU = 0 (ideal gas), q = -w

Did You Know?

⚛️

Internal energy is a state function—path independent.

Source: Thermodynamics

🌡️

For ideal gases, ΔU = 0 in isothermal processes.

Source: Kinetic theory

🔥

Adiabatic: q = 0, so ΔU = w (work only).

Source: First law

📊

Isochoric: w = 0, so ΔU = q (heat only).

Source: Constant volume

⚖️

Cv = (3/2)R monatomic, (5/2)R diatomic.

Source: Equipartition

💨

Joule expansion: free expansion has ΔU = 0 for ideal gas.

Source: Joule experiment

How the Internal Energy Calculator Works

Enter heat (q) and work (w) for first law; or moles, Cv, and ΔT for ideal gas; or P, V₁, V₂ for work calculation.

First Law

ΔU = q + w — heat + work

Ideal Gas

ΔU = nCvΔT — U depends only on T

Expert Tips

Sign Conventions

q > 0: heat in; w > 0: work on system.

Cv Values

Monatomic: 12.5; diatomic: 20.8 J/(mol·K).

Process Type

Select isothermal, adiabatic, isochoric, or isobaric.

Units

Use J or kJ consistently; convert P to Pa.

Process Comparison

ProcessConstraintΔU
IsothermalT constant0 (ideal gas)
Adiabaticq = 0w
IsochoricV constantq
IsobaricP constantq + w

Frequently Asked Questions

What is internal energy?

Total energy in a system: kinetic + potential of molecules. State function.

What is the first law?

ΔU = q + w. Energy change equals heat plus work.

Why ΔU = 0 for isothermal ideal gas?

U depends only on T for ideal gases; T constant ⇒ ΔU = 0.

What is w = -PΔV?

Work done BY system at constant P. Expansion (ΔV > 0) ⇒ w < 0.

When is heat capacity Cv used?

For constant-volume processes. ΔU = nCvΔT for ideal gas.

What is adiabatic?

No heat exchange (q = 0). All energy change from work.

How to find work from P-V?

w = -∫P dV. For constant P: w = -PΔV.

Key Numbers

8.314
R (J/(mol·K))
12.5
Cv monatomic (J/(mol·K))
20.8
Cv diatomic (J/(mol·K))
101325
1 atm (Pa)

📚 Official Sources

⚠️ Disclaimer: This calculator uses thermodynamic equations. For precise work, consult NIST Chemistry WebBook and IUPAC Gold Book.

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