Standard electrode potential
E° measured under standard conditions (1 M, 1 bar, 298 K) relative to standard hydrogen electrode (SHE, E° = 0). Higher E°: stronger oxidising agent.
-- NCERT, p. 20Every metal dipped into a solution of its own ions develops a potential difference at the metal-solution interface. This is the electrode potential — it measures a half-cell's tendency to gain electrons (get reduced). You cannot measure a single electrode's absolute potential; you always measure it relative to a reference.
The reference: the Standard Hydrogen Electrode (SHE) is assigned E° = 0.000 V at 298 K, 1 bar H₂, 1 M H⁺ (NCERT Class 12 Chemistry Chapter 2, page 6). Every other electrode potential in the electrochemical series is measured against SHE.
Convention trap that costs marks: NCERT and NEET use the reduction potential convention — all tabulated values are for the reduction half-reaction. When you calculate cell EMF:
E°_cell = E°(cathode) − E°(anode)
Both values are reduction potentials. Do NOT flip the sign of the anode value before subtracting — the subtraction already accounts for the reversal.
Moving beyond standard conditions: when concentrations differ from 1 M or temperature from 298 K, the Nernst equation adjusts the potential:
E = E° − (0.0591/n) × log₁₀ Q (at 298 K)
Here n is the number of electrons transferred in the balanced redox equation, and Q is the reaction quotient. A high-frequency trap: getting n wrong. For Zn²⁺/Zn vs Cu²⁺/Cu, the balanced equation transfers 2 electrons (n = 2). For Cr₂O₇²⁻ reduction in acid, n = 6. Always write the balanced equation first, then count electrons.
Watch-out: when Q = 1, log Q = 0 and E = E°. At equilibrium, E = 0 and Q = K. These limiting checks catch arithmetic errors fast.
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
The standard electrode potential of a half-cell is measured relative to which reference electrode?
In the IUPAC convention, the standard electrode potentials listed in the electrochemical series represent which type of potential?
At equilibrium, the cell potential E of an electrochemical cell equals:
Given: E°(Cu²⁺/Cu) = +0.34 V, E°(Zn²⁺/Zn) = −0.76 V. What is E°_cell for the Daniell cell (Zn anode, Cu cathode)?
For the cell Zn | Zn²⁺ (1 M) || Cu²⁺ (0.01 M) | Cu, how many electrons (n) should be used in the Nernst equation?
For a cell with E° = +0.46 V and n = 2, what is the cell EMF when the reaction quotient Q = 10 at 298 K? (Use: E = E° − (0.0591/n) log Q)
For the cell: Ag | Ag⁺ (0.001 M) || Ag⁺ (1 M) | Ag (a concentration cell), calculate E_cell at 298 K. E° for Ag⁺/Ag = +0.80 V.
A student calculates E_cell for a Daniell cell using the Nernst equation and obtains a negative value. Which of the following is the most likely interpretation?
Pattern: Nernst equation problem (NEET pattern: nernst equation problem)
Given
- E°(Cu²⁺/Cu) = +0.34 V - E°(Zn²⁺/Zn) = −0.76 V - [Zn²⁺] = 0.10 M - [Cu²⁺] = 2.0 M - T = 298 K
Required
E_cell at the given non-standard concentrations.
Concept
The Nernst equation adjusts the standard EMF for non-standard concentrations via the reaction quotient Q.
Formula
E°_cell = E°(cathode) − E°(anode) E = E° − (0.0591/n) × log₁₀ Q
Substitution
E°_cell = (+0.34) − (−0.76) = +1.10 V Balanced reaction: Zn(s) + Cu²⁺(aq) → Zn²⁺(aq) + Cu(s) n = 2 (Zn loses 2e⁻, Cu²⁺ gains 2e⁻) Q = [Zn²⁺]/[Cu²⁺] = 0.10/2.0 = 0.050 E = 1.10 − (0.0591/2) × log₁₀(0.050)
Calculation
log₁₀(0.050) = log₁₀(5.0 × 10⁻²) = log₁₀(5.0) + log₁₀(10⁻²) = 0.699 − 2 = −1.301 (0.0591/2) × (−1.301) = 0.02955 × (−1.301) = −0.03845 E = 1.10 − (−0.03845) = 1.10 + 0.03845 = 1.138 V Note on exact values: the integer 2 in n = 2 is a counting number (electrons per balanced equation) and does not limit significant figures. The factor 0.0591 is a derived constant (RT ln10 / F at 298 K) carrying 3 significant figures, which governs the precision of the correction term.
Final answer
E_cell = **1.14 V** (3 significant figures, limited by the 0.0591 factor).
Common trap
Using n = 1 instead of n = 2 would double the correction: (0.0591/1) × (−1.301) = −0.0769, giving E = 1.177 V — a wrong answer that appears on NEET option lists. Always count electrons from the balanced equation.
Similar NEET-style question
For the cell Fe | Fe²⁺ (0.01 M) || Ag⁺ (0.1 M) | Ag, calculate E_cell at 298 K. Given: E°(Fe²⁺/Fe) = −0.44 V, E°(Ag⁺/Ag) = +0.80 V. (Hint: balanced reaction transfers n = 2 electrons; Q = [Fe²⁺]/[Ag⁺]².) ---
E° measured under standard conditions (1 M, 1 bar, 298 K) relative to standard hydrogen electrode (SHE, E° = 0). Higher E°: stronger oxidising agent.
-- NCERT, p. 20E° = potential of electrode at unit activity (1 M for ions, 1 bar for gases, 298 K) relative to SHE (E° = 0 by definition). Higher E°: stronger tendency to be reduced.
-- NCERT Class 12 Chemistry, Ch. 2, p. 6Both 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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