ΔG = −nFE
Learn and apply ΔG = −nFE in the published Chemistry course sequence.
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The core idea
On this page
ΔG° = −nFE°: Orientation
This lesson connects electrochemistry to energetics: once you know E⦵_cell and the electron count n, you can use Δ G⦵ = -nF E⦵_cell to decide feasibility and calculate energy changes.
Before the harder applications, review Writing Redox Equations from Half-Equations and keep the Electrochemistry hub as your route map.
This page is really testing:
- Can you extract the correct n from a balanced redox equation?
- Can you do a clean units chain (J mol⁻¹ vs kJ mol⁻¹) without sign errors?
- Can you interpret signs correctly: positive E⦵_cell and negative Δ G⦵?
Definitions (Must Know)
A. Relationship between free energy and cell potential
Under standard conditions: Δ G⦵ = -nF E⦵_cell
Where:
- Δ G⦵ is the standard Gibbs free energy change (J mol⁻¹)
- n is the number of moles of electrons transferred per mole of reaction
- F is the Faraday constant (≈ 9.65 × 10⁴ C mol⁻¹)
- E⦵_cell is the standard cell potential (V)
Detailed Explanations
A. How to find n reliably
- Write the two half-equations.
- Balance electrons by multiplying.
- The number of electrons that cancel is n.
Mini example: For Zn + Cu²⁺ → Zn²⁺ + Cu, n = 2 (2 electrons transferred).
B. What the equation is telling you (in words)
Cell potential measures the “push” for electron flow. Δ G⦵ measures the maximum useful electrical work available per mole of reaction. The minus sign links a positive cell potential to a negative free energy change.
C. Worked calculation method (exam-safe order)
- Find or calculate E⦵_cell first.
- Determine n from the balanced electron transfer.
- Substitute into Δ G⦵ = -nFE⦵_cell with F = 9.65 × 10⁴ C mol⁻¹.
- Keep units in J mol⁻¹ during substitution.
- Convert to kJ mol⁻¹ only at the end if required.
- Add a sign interpretation sentence about feasibility under standard conditions.
Worked Examples
Modelled example 1
Calculate Standard Gibbs Energy
Problem
Study the worked solution
Apply the sign convention
Method
Use Δ G⦵ = -nFE⦵_cell.Reason
A positive cell potential corresponds to a negative standard Gibbs-energy change.Working
-(2)(9.65 × 10⁴)(1.10)Evaluate
Method
Calculate in joules, then convert if desired.Reason
Faraday’s constant is in C mol⁻¹ and V·C = J.Working
-2.12 × 10⁵ J mol⁻¹ = -212 kJ mol⁻¹
Quick check
Guided practice 2
Recover Cell Potential
Problem
Try this before viewing the solution
Hints
Hint 1: joules
Hint 2: subject
View solution step by step
Align units
Method
Convert Gibbs energy to joules per mole.Reason
F is expressed using coulombs, so the energy result pairs with joules.Working
Δ G⦵ = -145000 J mol⁻¹Rearrange
Method
Divide -Δ G⦵ by nF.Reason
The two negative signs give a positive potential.Working
E⦵ = 145000/(3)(9.65 × 10⁴) = 0.501 V
Quick check
Common misconception 3
Correct the Sign Inference
Learner claim
Try this before viewing the solution
View solution step by step
Fix signs of constants
Method
Recognise that n > 0 and F > 0.Reason
Only the leading minus sign reverses the sign of E⦵.Working
Δ G⦵ = -(positive)E⦵Infer direction
Method
Give E⦵_cell < 0 when Δ G⦵ > 0.Reason
The two quantities have opposite signs.Working
Δ G⦵ > 0 ⇒ E⦵_cell < 0
Common mistake
Examiner practice 4
Handle a Scaled Cell Reaction
Problem
Try this before viewing the solution
View solution step by step
Use reaction electron count
1 markMethod
Set n = 4 for the equation as written.Reason
Gibbs energy is extensive and scales with stoichiometric electron transfer.Working
Δ G⦵ = -nFE⦵Substitute
1 markMethod
Use the unchanged intensive cell potential.Reason
Potential is not multiplied when the equation is scaled.Working
-(4)(9.65 × 10⁴)(0.80)State result
1 markMethod
Report energy per mole of reaction as written.Reason
The calculation gives the extensive energy change for that stoichiometry.Working
-3.09 × 10⁵ J mol⁻¹
Self-mark with the mark scheme
Compare your response with each mark point. Select a point only when your response contains that evidence.
Do not scale E°cell.
Challenge 5
Infer the Electron Count
Problem
Try this before viewing the solution
Hints
Hint 1: convert
Hint 2: rearrange
View solution step by step
Solve numerically
Method
Divide the positive magnitude by FE⦵.Reason
The signs cancel for a spontaneous forward reaction.Working
n = 193000/(9.65 × 10⁴)(1.00) = 2.00Interpret
Method
State two electrons per reaction as written.Reason
n is a stoichiometric electron count and should agree with the balanced redox equation.Working
n = 2
Quick check
Common Mistakes
- Using the wrong n (forgetting to multiply half-equations first).
- Mixing units (kJ mol⁻¹ vs J mol⁻¹).
- Using a non-standard cell potential in a standard equation (the ⦵ symbols matter).
- Dropping the negative sign in rearrangements.
- Treating a negative Δ G⦵ as “fast”; this equation is about feasibility, not rate.
When you can explain this confidently, use the Electrochemistry quiz and the Exam Skills hub to pressure-test exam wording.
Exam Tips
- If the question uses kJ mol⁻¹, convert at the end: 1 kJ = 1000 J.
- Always show the value of n and where it comes from (electron balance).
- Don’t change E⦵ signs by multiplying; only reverse sign if you reverse the half-equation direction.
- Strong conclusion line: “Since Δ G⦵ is negative, the reaction is thermodynamically feasible under standard conditions.”
- If solving for E⦵_cell, state “from Δ G⦵ = -nFE⦵_cell, rearrange to E⦵_cell = -Δ G⦵/(nF).”
Mind Stretchers
Mind stretcher 1Extension
Why is E⦵_cell independent of how you balance the overall equation, but n changes when you scale the equation?
Show Hint
Classify each quantity as intensive or extensive before thinking about equation scaling.
Show Answer
Mark scheme:
- E⦵_cell depends on the difference between two intensive half-cell potentials, so it does not scale with amount of substance.
- n is tied to the stoichiometric amount of electrons transferred per mole of reaction as written, so it scales when you multiply the equation.
Mind stretcher 2: Scaling a cell reaction without scaling its voltageExtension
Question. A balanced cell reaction has E⦵_cell = +0.62 V, n = 2 and Δ G⦵ = -120 kJ mol⁻¹ to the stated precision. The entire equation is doubled. State the new values of E⦵_cell, n and Δ G⦵, and explain the pattern.
Show Hint
Voltage is intensive; electron amount and free-energy change follow the stoichiometric scale of the reaction as written.
Show Answer
E⦵_cell remains + 0.62 V because electrode potential is intensive. The electron count becomes n = 4, and Δ G⦵ becomes -240 kJ mol⁻¹ because the amount of reaction and maximum electrical work have doubled. This keeps Δ G⦵ = -nFE⦵_cell consistent.