Galvanic vs electrolytic cells
Galvanic (voltaic): chemical → electrical energy (spontaneous, ΔG<0). Electrolytic: electrical → chemical (non-spontaneous, ΔG>0; external EMF needed).
-- NCERT Class 12 Chemistry, Ch. 2, p. 4An electrochemical cell converts chemical energy into electrical energy (galvanic cell) or uses electrical energy to drive a non-spontaneous reaction (electrolytic cell). NEET questions on this topic test whether you can distinguish the two types and correctly assign electrode polarity, electrode names, and the sign convention for cell EMF.
The trap that costs marks: confusing which electrode is the anode and which is the cathode across galvanic and electrolytic cells. In a galvanic cell, oxidation occurs at the anode (negative terminal); in an electrolytic cell, oxidation still occurs at the anode, but the anode is now the positive terminal (connected to the positive terminal of the external battery). The chemistry definition — anode = oxidation, cathode = reduction — never changes. The polarity does.
Galvanic (voltaic) cell. Two half-cells connected by a salt bridge. Oxidation at the anode releases electrons that flow through the external circuit to the cathode, where reduction occurs. The salt bridge maintains electrical neutrality by allowing ion migration. Cell representation uses the convention: anode on the left, cathode on the right, single vertical line for phase boundary, double vertical line for the salt bridge.
Example: the Daniell cell — Zn(s) | Zn²⁺(aq) || Cu²⁺(aq) | Cu(s). Zinc is oxidised (anode, negative terminal); copper ions are reduced (cathode, positive terminal).
Standard cell EMF is calculated as E°_cell = E°_cathode − E°_anode, using standard reduction potentials for both electrodes (NCERT Class 12 Chemistry Chapter 2, page 4). A positive E°_cell means the cell reaction is spontaneous under standard conditions.
Electrolytic cell. A single container with two electrodes dipped in an electrolyte, driven by an external power source. The external battery forces electrons to flow in the non-spontaneous direction. Anode (positive, connected to + terminal) undergoes oxidation; cathode (negative, connected to − terminal) undergoes reduction.
Watch-out: when NEET gives you a cell diagram without labelling which type it is, check for a salt bridge (galvanic) versus an external battery (electrolytic) before assigning terminal polarity.
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
In any electrochemical cell, oxidation always occurs at the:
Which component in a galvanic cell maintains electrical neutrality of the solutions in the two half-cells?
In an electrolytic cell, the anode is connected to the:
For the Daniell cell: Zn(s) | Zn²⁺(1 M) || Cu²⁺(1 M) | Cu(s), given E°(Zn²⁺/Zn) = −0.76 V and E°(Cu²⁺/Cu) = +0.34 V, the standard EMF of the cell is:
In the cell notation Ag(s) | Ag⁺(aq) || Cu²⁺(aq) | Cu(s), which species is being oxidised?
A student sets up a galvanic cell and an electrolytic cell side by side. In the galvanic cell, the anode carries a ______ charge; in the electrolytic cell, the anode carries a ______ charge.
If the standard cell EMF for a proposed galvanic cell comes out to be −0.15 V, what does this indicate?
A student argues that in an electrolytic cell, the cathode is where oxidation occurs because the cathode is connected to the negative terminal. Which part of this reasoning is incorrect?
Given
A galvanic cell is constructed with the following half-cells: - Fe(s) | Fe²⁺(1 M) — E°(Fe²⁺/Fe) = −0.44 V - Ag⁺(1 M) | Ag(s) — E°(Ag⁺/Ag) = +0.80 V
Required
(a) Write the cell notation. (b) Calculate E°_cell. (c) Identify the direction of electron flow.
Concept
In a galvanic cell, the electrode with the lower (more negative) reduction potential acts as the anode (oxidation). The electrode with the higher reduction potential acts as the cathode (reduction). Cell notation: anode on the left, cathode on the right.
Formula
E°_cell = E°_cathode − E°_anode
Substitution
E°_cathode = E°(Ag⁺/Ag) = +0.80 V E°_anode = E°(Fe²⁺/Fe) = −0.44 V E°_cell = (+0.80) − (−0.44)
Calculation
E°_cell = 0.80 + 0.44 = +1.24 V Note: the reduction potential values (−0.44 V and +0.80 V) are exact standard table values used as given data. They do not introduce significant-figure considerations.
Final answer
(a) Cell notation: Fe(s) | Fe²⁺(1 M) || Ag⁺(1 M) | Ag(s) (b) E°_cell = +1.24 V (c) Electrons flow from the iron electrode (anode) through the external circuit to the silver electrode (cathode). Since E°_cell > 0, the cell reaction is spontaneous under standard conditions.
Common trap
Subtracting in the wrong direction: E°_anode − E°_cathode = (−0.44) − (0.80) = −1.24 V. A negative result would falsely suggest the reaction is non-spontaneous. Always compute cathode minus anode.
Similar NEET-style question
Given E°(Ni²⁺/Ni) = −0.25 V and E°(Cu²⁺/Cu) = +0.34 V, construct the cell notation for a spontaneous galvanic cell and calculate E°_cell. Answer: Ni(s) | Ni²⁺(1 M) || Cu²⁺(1 M) | Cu(s); E°_cell = +0.34 − (−0.25) = +0.59 V. ---
Galvanic (voltaic): chemical → electrical energy (spontaneous, ΔG<0). Electrolytic: electrical → chemical (non-spontaneous, ΔG>0; external EMF needed).
-- NCERT Class 12 Chemistry, Ch. 2, p. 4Both 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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