ΔG and EMF
ΔG = -nFE; ΔG° = -nFE° = -RT ln K. n = electrons transferred, F = Faraday's constant (96485 C/mol).
-- NCERT Class 12 Chemistry, Ch. 2, p. 14The relationship ΔG° = −nFE° is where thermodynamics meets electrochemistry — and the most common leak here is a sign error. A positive E°_cell means the reaction is spontaneous (ΔG° < 0), and a negative E°_cell means non-spontaneous (ΔG° > 0). The minus sign in the formula enforces this: forget it, and every spontaneity prediction flips.
The core formula (NCERT Class 12 Chemistry Chapter 2, page 14):
ΔG° = −nFE°_cell
where n = number of electrons transferred in the balanced redox equation, F = 96485 C/mol (Faraday's constant), and E°_cell = standard cell EMF in volts.
How to get E°_cell: Both half-cell potentials must be written as reductions. Then E°_cell = E°_cathode − E°_anode. If E°_cell comes out positive, the cell works spontaneously; if negative, you need external energy.
Unit check. ΔG° comes out in joules (C/mol × V = J/mol). NEET options sometimes list kJ/mol — divide by 1000. A common error is reporting the answer in joules when options are in kilojoules, or vice versa.
The equilibrium link. At equilibrium, ΔG = 0 and therefore E = 0. This connects to the Nernst equation (covered in its own lesson) but the takeaway here is: when a cell's potential drops to zero, the reaction has reached equilibrium and no further net work is possible.
What to watch for in NEET questions: Problems typically give two standard reduction potentials and ask for ΔG°. The sequence is always: (1) identify cathode and anode, (2) compute E°_cell, (3) determine n from the balanced equation, (4) plug into ΔG° = −nFE°. Errors cluster at steps 2 and 3 — reversing cathode/anode or miscounting electrons.
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
For a galvanic cell operating under standard conditions, what is the relationship between Gibbs energy change (ΔG°) and the standard cell EMF (E°_cell)?
If a cell has E°_cell > 0, what can be said about ΔG° for the cell reaction?
The value of one Faraday constant (F) is:
Given the standard reduction potentials: E°(Cu²⁺/Cu) = +0.34 V and E°(Zn²⁺/Zn) = −0.76 V. What is E°_cell for the Daniell cell (Zn anode, Cu cathode)?
For a cell reaction where n = 2 and E°_cell = +0.34 V, the standard Gibbs energy change ΔG° is: (F = 96485 C/mol)
A cell reaction has ΔG° = −193.0 kJ/mol and n = 2. What is E°_cell? (F = 96485 C/mol)
Given: E°(Ag⁺/Ag) = +0.80 V, E°(Cu²⁺/Cu) = +0.34 V. For the cell Cu | Cu²⁺ || Ag⁺ | Ag, what is ΔG° for the overall reaction Cu + 2Ag⁺ → Cu²⁺ + 2Ag? (F = 96485 C/mol)
When a galvanic cell operates and the reaction reaches equilibrium, what are the values of E_cell and ΔG?
Given
- E°(Zn²⁺/Zn) = −0.76 V (reduction potential) - E°(Cu²⁺/Cu) = +0.34 V (reduction potential) - F = 96485 C/mol
Required
ΔG° for the overall cell reaction, in kJ/mol.
Concept
The Gibbs energy change is related to cell EMF by ΔG° = −nFE°_cell (NCERT Class 12 Chemistry Chapter 2, page 14). We first need E°_cell from the two reduction potentials, then determine n from the balanced equation.
Formula
E°_cell = E°_cathode − E°_anode ΔG° = −nFE°_cell
Substitution
Zn is oxidized (anode), Cu²⁺ is reduced (cathode). E°_cell = (+0.34) − (−0.76) = +1.10 V Balanced half-reactions: - Zn → Zn²⁺ + 2e⁻ (oxidation) - Cu²⁺ + 2e⁻ → Cu (reduction) Therefore n = 2. ΔG° = −(2)(96485)(1.10)
Calculation
ΔG° = −(2)(96485)(1.10) ΔG° = −(2)(106133.5) ΔG° = −212267 J/mol ΔG° = −212.3 kJ/mol Note: n = 2 is an exact integer (electrons counted from the balanced equation) and F = 96485 C/mol is a defined constant. Neither limits significant figures. The precision is governed by the given reduction potentials (3 significant figures), so the answer is reported to 4 significant figures as −212.3 kJ/mol.
Final answer
**ΔG° = −212.3 kJ/mol** The negative value confirms the Daniell cell reaction is spontaneous under standard conditions, consistent with the positive E°_cell.
Common trap
The most frequent error is reversing cathode and anode: computing E°_cell = (−0.76) − (0.34) = −1.10 V. This gives ΔG° = +212.3 kJ/mol, flipping the spontaneity prediction. Always identify the more positive reduction potential as the cathode. A second error: using n = 1 (per Ag-type half-reactions) when the balanced equation clearly transfers 2 electrons. Always write out both half-reactions and count electrons explicitly.
Similar NEET-style question
"Given E°(Fe³⁺/Fe²⁺) = +0.77 V and E°(I₂/I⁻) = +0.54 V, calculate ΔG° for the reaction 2Fe³⁺ + 2I⁻ → 2Fe²⁺ + I₂. (F = 96485 C/mol)." Approach: E°_cell = 0.77 − 0.54 = +0.23 V. n = 2 (each Fe³⁺ gains 1e⁻, two Fe³⁺ ions transfer 2e⁻ total). ΔG° = −(2)(96485)(0.23) = −44383 J ≈ −44.4 kJ/mol. ---
ΔG = -nFE; ΔG° = -nFE° = -RT ln K. n = electrons transferred, F = Faraday's constant (96485 C/mol).
-- NCERT Class 12 Chemistry, Ch. 2, p. 14Both as reduction potentials. E°_cell > 0 → spontaneous.
| Symbol | Quantity | SI Unit |
|---|---|---|
| E°_cell | standard cell EMF | V |
| E°_red | reduction potential | V |
Mass deposited at electrode. M = molar mass; I = current; t = time; n = electrons per ion.
| Symbol | Quantity | SI Unit |
|---|---|---|
| m | mass deposited | g |
| M | molar mass | g/mol |
| I | current | A |
| t | time | s |
| n | electrons per ion | - |
| F | Faraday | C/mol |
Connection between thermodynamics and electrochemistry. F = 96485 C/mol.
| Symbol | Quantity | SI Unit |
|---|---|---|
| ΔG | Gibbs energy change | J |
| n | electrons transferred | - |
| F | Faraday 96485 | C/mol |
| E | cell EMF | V |
Molar conductivity from specific conductance. Increases with dilution as more ions are free.
| Symbol | Quantity | SI Unit |
|---|---|---|
| Λ_m | molar conductivity | S cm^2/mol |
| κ | specific conductance | S/cm |
| C | molarity | mol/L |
Cell potential at non-standard conditions. n = electrons transferred. At equilibrium E=0, Q=K.
| Symbol | Quantity | SI Unit |
|---|---|---|
| E | cell potential | V |
| E° | standard | V |
| n | electrons | - |
| Q | reaction quotient | - |
These are the exact patterns that cause wrong answers in NEET. Each trap includes when it triggers and how to avoid it.
Category: Negative Marking
Multi-step Nernst problem: identify electrons, write Q correctly, plug into 0.0591/n. Each sub-step has factor errors.
Cell EMF problem at non-standard conditions.
Step-by-step: (1) write balanced redox; (2) count n electrons; (3) compute Q from concentrations; (4) plug into Nernst. Verify by checking limits: at standard conditions Q=1, log Q=0, E=E°.
Category: Inorganic Exception
Student assumes Mn²⁺ is the product regardless of medium. Acidic: → Mn²⁺ (5e⁻). Neutral/weakly basic: → MnO₂ (3e⁻). Strongly basic: → MnO₄²⁻ (1e⁻).
Question gives KMnO4 oxidation in unspecified or specific medium.
Always check medium. In acidic: Mn(+7) → Mn(+2). In neutral: → Mn(+4) (MnO₂). In basic: → Mn(+6) (manganate). The number of electrons (n) in Nernst calculations depends accordingly.
Root cause: concept gap
n = number of electrons per ion to deposit. Cu²⁺ + 2e⁻ → Cu: n=2. Al³⁺ + 3e⁻: n=3. m = MIt/(nF).
Root cause: formula misuse
n = electrons transferred per balanced redox equation. For Cu²⁺ + 2e⁻ → Cu: n=2. For Mn(VII) → Mn(II): n=5.
17 questions from NEET 2021, 2022, 2023, 2024, 2025. Answers verified against NTA official keys.
The number of bonds, bonds and lone pair of electrons in pyridine, respectively are:
Which of the following statement is not correct about diborane?
Which one of the following polymers is prepared by addition polymerisation?
Recurring question shapes from past papers. Each pattern shows why wrong options look tempting.
inverts c multiplier
Uses Λ = κC instead of κ/C
forgets 1000 factor
Drops 1000 in unit conversion
wrong n electrons
Uses incorrect electron count from half-reactions
Test yourself on this topic with real past-paper questions:
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