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 Class 11 Chemistry, Ch. 7, p. 250Every 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 34). 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?
Answer: C. By IUPAC convention, the standard hydrogen electrode (SHE) is assigned E° = 0.000 V and serves as the universal reference for all standard electrode potentials (NCERT Class 12 Chemistry Chapter 2, page 34).
Why A is wrong: A is wrong because the calomel electrode is a secondary reference electrode used in laboratory practice; it is not the IUPAC-defined primary reference. Its own potential (+0.242 V) is measured against SHE.
Why B is wrong: B is wrong because the Ag/AgCl electrode is another secondary reference. Like calomel, its potential is defined relative to SHE, not the other way around.
Why D is wrong: D is wrong because no 'saturated copper electrode' is an established reference standard. This is a fabricated distractor.
In the IUPAC convention, the standard electrode potentials listed in the electrochemical series represent which type of potential?
Answer: D. IUPAC convention tabulates all standard electrode potentials as reduction potentials — the potential for the half-reaction written as a reduction (NCERT Class 12 Chemistry Chapter 2, page 34).
Why A is wrong: A is wrong because the oxidation potential convention (used in older American textbooks) is the negative of the reduction potential. IUPAC and NCERT use reduction potentials exclusively.
Why B is wrong: B is wrong because decomposition potential refers to the minimum voltage needed to electrolyse a compound — an electrolysis concept, not a thermodynamic electrode property.
Why C is wrong: C is wrong because cell potential is the difference between two half-cell potentials, not a property of a single electrode.
At equilibrium, the cell potential E of an electrochemical cell equals:
Answer: A. At equilibrium the driving force for the net reaction is zero, so E = 0. From the Nernst equation, when E = 0 the reaction quotient Q equals the equilibrium constant K (NCERT Class 12 Chemistry Chapter 2, page 34).
Why B is wrong: B is wrong because E° is the standard cell potential (at Q = 1). At equilibrium Q = K ≠ 1 (for a spontaneous cell), so E ≠ E°.
Why C is wrong: C is wrong because +1 V is an arbitrary value with no thermodynamic basis at equilibrium.
Why D is wrong: D is wrong because −nF has units of C/mol (charge), not volts. This confuses the ΔG = −nFE relationship with the cell potential itself.
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)?
Answer: B. E°_cell = E°(cathode) − E°(anode) = (+0.34) − (−0.76) = +1.10 V. Both values enter as reduction potentials; the formula handles the sign reversal (NCERT Class 12 Chemistry Chapter 2, page 34).
Why A is wrong: A is wrong because +0.42 V results from adding the two potentials with wrong signs — typically from flipping the cathode sign instead of subtracting the anode reduction potential directly.
Why C is wrong: C is wrong because −1.10 V reverses cathode and anode in the formula (subtracts cathode from anode). A negative E°_cell would mean the reaction is non-spontaneous, contradicting the known spontaneity of the Daniell cell.
Why D is wrong: D is wrong because −0.42 V combines both errors: wrong subtraction order and wrong sign handling.
For the cell Zn | Zn²⁺ (1 M) || Cu²⁺ (0.01 M) | Cu, how many electrons (n) should be used in the Nernst equation?
Answer: A. The balanced cell reaction is Zn + Cu²⁺ → Zn²⁺ + Cu. Each Zn atom loses 2 electrons and each Cu²⁺ gains 2 electrons, so n = 2. This is determined from the balanced redox equation, not from the stoichiometric coefficients of the ions alone.
Why B is wrong: B is wrong because n = 1 would apply only to a one-electron transfer process (e.g., Ag⁺/Ag). For Cu²⁺ + 2e⁻ → Cu, two electrons transfer per formula unit. Using n = 1 doubles the Nernst correction term and gives an incorrect EMF (trap: nernst n electrons negmark).
Why C is wrong: C is wrong because n = 3 corresponds to a three-electron process (e.g., Al³⁺/Al). Neither Zn²⁺/Zn nor Cu²⁺/Cu involves a 3-electron transfer.
Why D is wrong: D is wrong because n = 4 would require a four-electron balanced equation. No single Zn or Cu half-reaction transfers 4 electrons.
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)
Answer: D. E = 0.46 − (0.0591/2) × log₁₀(10) = 0.46 − 0.02955 × 1 = 0.430 V (3 s.f.). The Nernst correction is (0.0591/2) × 1 = 0.02955 V.
Why A is wrong: A is wrong because +0.46 V is the standard EMF (at Q = 1). When Q = 10, the Nernst correction is non-zero, so E < E°.
Why B is wrong: B is wrong because +0.519 V makes two slips: it adds the correction instead of subtracting it, and uses n = 1: 0.46 + 0.0591 = 0.519. When Q > 1 the correction lowers E.
Why C is wrong: C is wrong because +0.401 V results from using n = 1 instead of n = 2 in the Nernst equation: 0.46 − 0.0591 × 1 = 0.401. This is the classic n-electron error (trap: nernst n electrons negmark).
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.
Answer: C. For a concentration cell, E°_cell = 0 (same electrodes). The Nernst equation gives E = 0 − (0.0591/1) × log₁₀(0.001/1) = −0.0591 × (−3) = +0.177 V. Here n = 1 (Ag⁺ + e⁻ → Ag), and Q = [Ag⁺]_anode / [Ag⁺]_cathode = 0.001/1 = 10⁻³.
Why A is wrong: A is wrong because E = 0 V would be the case only if both compartments had the same concentration. The concentration difference is the driving force of this cell.
Why B is wrong: B is wrong because +0.0591 V results from using log₁₀(0.001) = −3 but then dividing by n = 3 instead of n = 1, or equivalently using log₁₀(0.1) = −1 with n = 1. The Ag⁺/Ag half-reaction is a one-electron process.
Why D is wrong: D is wrong because +0.80 V is the standard reduction potential of Ag⁺/Ag. In a concentration cell, E°_cell = 0 (both electrodes are identical), so the standard potential of the individual half-cell does not appear as the cell EMF.
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?
Answer: B. A negative E_cell means the forward reaction is non-spontaneous under those specific conditions — the reaction proceeds spontaneously in the reverse direction. This can happen at extreme concentration ratios (very large Q), even for a Daniell cell whose E° is positive.
Why A is wrong: A is wrong because at equilibrium E = 0 exactly, not a negative value. A negative E_cell indicates the system is past equilibrium for the forward reaction.
Why C is wrong: C is wrong because while E° for the Daniell cell is positive (+1.10 V), the actual EMF under non-standard conditions depends on Q. If Q is extremely large (products heavily favoured), E can become negative via the Nernst equation.
Why D is wrong: D is wrong because temperature alone does not determine the sign of E_cell. The Nernst equation at temperatures other than 298 K uses RT/nF instead of 0.0591/n, but Q is the dominant factor driving E negative.
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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.)
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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 Class 11 Chemistry, Ch. 7, p. 250E° = 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. 36More in Redox Reactions and Electrochemistry: 4 exam traps and mistakes · 5 formulas · 2 question patterns from its other lessons.
2 questions from NEET 2022, 2026. Answers verified against NTA official keys.
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