Q.Arrange the following metals in the order in which they displace each other from the solution of their salts:
Al, Cu, Fe, Mg and Zn.
Concept understanding — Galvanic Corrosion
Galvanic Corrosion: From Intuition to Precision
Imagine you have two different metals — say, a copper pipe and an iron nail — and you connect them with a wire, then dip both into a bucket of salt water. If you come back a few hours later, the iron nail will be badly rusted, while the copper pipe will look almost untouched. Why?
The answer is galvanic corrosion. It is the accelerated corrosion of one metal when it is in electrical contact with a different metal in the presence of an electrolyte (like water with dissolved salts).
The Intuition: A "Battery" That Eats Metal
Think of a simple battery: you have two different metals (electrodes) and a chemical solution (electrolyte). One metal wants to give away electrons (it gets eaten away), and the other wants to accept them (it stays protected). That is exactly what happens in galvanic corrosion.
- The more reactive metal (the one that "wants" to corrode) becomes the anode. It loses electrons and dissolves into the electrolyte — that is the corrosion you see.
- The less reactive metal becomes the cathode. It does not corrode; instead, it accepts electrons from the anode, often causing the electrolyte near it to become alkaline or to produce hydrogen gas.
The key point: the two metals do not need to be physically touching. They just need electrical contact (through a wire or direct contact) and a continuous electrolyte (water, soil, concrete, etc.) to complete the circuit.
The Precise Statement
Galvanic corrosion is the electrochemical process in which a more active metal (the anode) corrodes preferentially when electrically coupled to a less active metal (the cathode) in the presence of an electrolyte. The driving force is the difference in their electrode potentials.
The Galvanic Series: The "Who Eats Whom" Chart
Not all metal pairs corrode equally. The galvanic series ranks metals and alloys by their tendency to corrode in seawater (a common electrolyte). The more negative (active) a metal is, the more likely it is to be the anode and corrode.
Here is a simplified version of the series (from most active/anodic to most noble/cathodic):
| Metal / Alloy | Relative Activity |
|---|---|
| Magnesium | Most active (anodic) |
| Zinc | |
| Aluminium | |
| Cadmium | |
| Mild steel / Iron | |
| Stainless steel (active) | |
| Tin | |
| Lead | |
| Copper | |
| Nickel | |
| Stainless steel (passive) | |
| Silver | |
| Titanium | |
| Gold / Platinum | Most noble (cathodic) |
A common mistake: students think the larger metal always corrodes. In reality, it is the more active metal that corrodes, regardless of size. However, the area ratio matters enormously — a small anode coupled to a large cathode corrodes very fast (like a tiny iron rivet holding a huge copper plate).
The Three Conditions for Galvanic Corrosion
For galvanic corrosion to occur, all three must be present:
- Two dissimilar metals (or the same metal in different environments, e.g., a steel pipe in soil vs. in air).
- Electrical contact between them (direct physical contact or through a wire).
- An electrolyte bridging them (water, moisture, soil, concrete, etc.).
Remove any one, and galvanic corrosion stops.
Real-World Examples
- The Statue of Liberty: The copper skin was originally separated from the iron framework by asbestos cloth. When the cloth degraded, the iron (anode) corroded rapidly because it was coupled to the huge copper (cathode) surface.
- Plumbing: Connecting a copper pipe directly to a galvanized steel pipe causes the steel to corrode near the joint.
- Marine environments: Aluminium boat hulls with bronze propellers — the aluminium corrodes unless protected by sacrificial anodes (zinc blocks).
How to Prevent It
- Avoid dissimilar metal contact where possible.
- Insulate the two metals with a non-conductive gasket or coating.
- Use a sacrificial anode — attach a more active metal (like zinc) that corrodes instead of the structure you want to protect.
- Coat both metals with paint or sealant, but be careful: if the coating on the anode is damaged, corrosion concentrates at the defect.
The same principle is used deliberately in cathodic protection — for example, zinc blocks are bolted to ship hulls or underground pipelines. The zinc corrodes sacrificially, protecting the steel.
The Bottom Line
Galvanic corrosion is not magic — it is simply a galvanic cell (a battery) where the anode metal is the "fuel" that gets consumed. The greater the difference in the galvanic series between the two metals, the stronger the driving force, and the faster the corrosion.
Galvanic corrosion is discussed in the NCERT/CBSE Class 12 Chemistry chapter on Electrochemistry, and ‘galvanic corrosion vs rusting’ or ‘sacrificial anode protection’ are frequently searched important-question topics for board exams and JEE Main. Understanding this electrochemical-cell-based explanation of corrosion is also useful for application-based NEET and CET chemistry questions.
Why this formula?
Galvanic Corrosion: Why the Key Formulas Hold
Galvanic corrosion occurs when two dissimilar metals are electrically connected in the presence of an electrolyte. The key formula that governs this is the mixed potential theory, which leads to the galvanic current and corrosion rate expressions.
Let's build the reasoning step-by-step.
1. The Core Idea: Two Electrodes, One Circuit
When metals M₁ (more active, e.g., zinc) and M₂ (more noble, e.g., copper) are connected:
- M₁ acts as the anode — it oxidizes (corrodes):
M1→M1n++ne−
- M₂ acts as the cathode — it reduces something (e.g., oxygen or H⁺):
O2+2H2O+4e−→4OH−(in neutral/alkaline)
or
2H++2e−→H2(in acidic)
The two metals are electrically connected (via a wire or direct contact), and the electrolyte completes the circuit. Electrons flow from M₁ to M₂.
2. The Mixed Potential: Why It Exists
Each metal, when alone in the electrolyte, has its own open-circuit potential (OCP) — the equilibrium potential for its half-reaction. For M₁, it's Ecorr,1; for M₂, it's Ecorr,2.
When connected, the system cannot stay at two different potentials. The entire metal couple must reach a single potential — the mixed potential Emix.
- Emix lies between Ecorr,1 and Ecorr,2.
- At Emix, the total anodic current from M₁ equals the total cathodic current from M₂ (charge conservation):
Ianode=Icathode
This is the fundamental equation of galvanic corrosion.
3. Deriving the Galvanic Current
Assume each electrode follows Butler-Volmer kinetics (for activation-controlled reactions). For the anode (M₁), the anodic current density ia at potential E is:
ia=i0,1exp(RTαaF(E−E0,1))
For the cathode (M₂), the cathodic current density ic is:
ic=i0,2exp(−RTαcF(E−E0,2))
Where:
- i0,1,i0,2 = exchange current densities
- αa,αc = transfer coefficients (typically ~0.5)
- F = Faraday constant
- R = gas constant
- T = temperature
- E0,1,E0,2 = standard reduction potentials
At the mixed potential Emix:
Igalvanic=A1⋅ia(Emix)=A2⋅ic(Emix)
Where A1 and A2 are the surface areas of the anode and cathode.
Why this holds: The net current from the anode must exactly balance the net current consumed at the cathode — otherwise, charge would accumulate, which is impossible in a steady-state circuit.
4. The Corrosion Rate Formula
The corrosion rate (mass loss per time) of the anode is given by Faraday's law:
Corrosion rate=n⋅F⋅ρIgalvanic⋅M
Where:
- M = molar mass of the anode metal
- n = number of electrons transferred per atom
- ρ = density of the metal
- F = Faraday constant (96,485 C/mol)
Why this holds: Each mole of metal oxidized releases n moles of electrons. The total charge passed Q=Igalvanic⋅t corresponds to moles of metal lost:
moles lost=nFQ=nFIgalvanic⋅t
Multiply by M/ρ to get volume or thickness loss.
5. The Area Effect: Why It Matters
From the mixed potential equation:
A1⋅ia(Emix)=A2⋅ic(Emix)
If the cathode area A2 is large relative to the anode area A1, then ia(Emix) must be large to balance the current. This means:
- Small anode + large cathode → severe galvanic corrosion (high current density on the anode).
- Large anode + small cathode → mild corrosion.
Why this holds: The current density on the anode is ia=Igalvanic/A1. For a fixed Igalvanic, smaller A1 gives higher ia, which accelerates corrosion.
6. The Driving Force: Potential Difference
The driving force for galvanic corrosion is the difference in open-circuit potentials:
ΔE=Ecorr,2−Ecorr,1
A larger ΔE generally leads to a larger Igalvanic, but the exact relationship depends on the polarization behavior (Tafel slopes) of both electrodes.
Why this holds: The mixed potential Emix is determined by the intersection of the anodic and cathodic polarization curves. A larger separation between the two curves shifts the intersection to a higher current.
Summary of Key Takeaways
| Concept | Formula | Why It Holds |
|---|---|---|
| Mixed potential | Ianode=Icathode | Charge conservation in a closed circuit |
| Galvanic current | A1ia(Emix)=A2ic(Emix) | Butler-Volmer kinetics + area balance |
| Corrosion rate | nFρIgalvanicM | Faraday's law of electrolysis |
| Area effect | Small anode → high ia | Current density inversely proportional to area |
| Driving force | ΔE=Ecorr,2−Ecorr,1 | Larger potential difference → larger current (generally) |
Exam tip: Always start with the mixed potential condition — it's the foundation. Then apply Faraday's law for the rate. Never forget the area ratio — it's the most common trick in exam problems.
The key idea is the reactivity series of metals — a more reactive metal will displace a less reactive metal from the solution of its salt.
Reasoning:
- Recall the standard reactivity series (most to least reactive): Mg > Al > Zn > Fe > Cu.
- A metal higher in the series can displace any metal below it from its salt solution.
- Therefore, the order of displacement ability is the same as the reactivity series.
The order of displacement is Mg>Al>Zn>Fe>Cu.
The order of displacement is determined by the standard reduction potentials (reactivity series). The most reactive metal (Mg) displaces all others, while the least reactive (Cu) displaces none. The final order of displacement is: Mg > Al > Zn > Fe > Cu.
Why This Works — The Concept of Galvanic Corrosion (Displacement)
When a metal is placed in a solution of a salt of another metal, a displacement reaction occurs if the more reactive metal (the one that loses electrons more easily) is the solid. The more reactive metal acts as the anode (oxidised), while the ions of the less reactive metal in solution get reduced and plate out as the solid metal.
Think of it as a tug-of-war for electrons. The metal with a more negative standard reduction potential (or a lower position in the electrochemical series) holds its electrons less tightly — it is more willing to give them away. So it will "kick out" any metal ion that has a less negative (more positive) reduction potential.
The standard reduction potentials (at 25°C) for the half-reactions involved are:
| Metal | Half-reaction | E∘ (V) |
|---|---|---|
| Mg | Mg2++2e−→Mg | −2.37 |
| Al | Al3++3e−→Al | −1.66 |
| Zn | Zn2++2e−→Zn | −0.76 |
| Fe | Fe2++2e−→Fe | −0.44 |
| Cu | Cu2++2e−→Cu | +0.34 |
The more negative the E∘, the stronger the reducing agent (the metal is more reactive). So the reactivity order from most reactive to least is: Mg > Al > Zn > Fe > Cu.
A common mistake is to think that a metal with a more positive reduction potential is more reactive. That is the opposite of the truth. A more positive E∘ means the metal ion is more easily reduced — meaning the metal itself is less reactive (it holds onto its electrons tightly).
Step-by-Step Reasoning
1. Identify the most reactive metal.
From the list, Mg has the most negative E∘ (−2.37 V). It will displace every other metal from their salt solutions. For example:
Mg+Cu2+→Mg2++Cu
Mg+Fe2+→Mg2++Fe
and so on.
2. Identify the next most reactive.
Al (−1.66 V) is less reactive than Mg but more reactive than Zn, Fe, and Cu. So Al will displace Zn, Fe, and Cu from their salts, but not Mg. For instance:
Al+Zn2+→Al3++Zn
but Al cannot displace Mg from Mg2+ because Mg is more reactive.
3. Continue down the series.
Zn (−0.76 V) will displace Fe and Cu, but not Mg or Al.
Fe (−0.44 V) will displace only Cu, but not Mg, Al, or Zn.
Cu (+0.34 V) is the least reactive — it cannot displace any of the others. In fact, Cu itself will be displaced by all the others.
4. Arrange the order of displacement.
The metal that displaces the most others is placed first. So the order in which they displace each other (from most displacing to least displacing) is exactly the reactivity series:
Mg>Al>Zn>Fe>Cu
You can remember this order using a mnemonic: "Mighty Al Zaps Fe Cu" — Mg, Al, Zn, Fe, Cu. The first metal in the list displaces all that come after it.
The order in which the metals displace each other from solutions of their salts is: Mg > Al > Zn > Fe > Cu.
Method: Electrochemical Series (Reactivity Series) Approach
This method uses the standard reduction potential (or reactivity) of metals to predict displacement reactions. A more reactive metal (higher on the reactivity series) will displace a less reactive metal from its salt solution.
Steps:
-
Recall the standard reactivity series for the given metals (from most reactive to least reactive):
- Mg (most reactive)
- Al
- Zn
- Fe
- Cu (least reactive)
-
Understand the displacement rule:
A metal can displace any metal below it in the series from its salt solution.
For example, Mg can displace Al, Zn, Fe, and Cu from their salts.
-
Arrange the metals in decreasing order of reactivity (this is the order of displacement ability):
- Mg → Al → Zn → Fe → Cu
-
Write the final order (from most displacing to least displacing):
- Mg > Al > Zn > Fe > Cu
Key Concept (Why this works):
- More reactive metals have a greater tendency to lose electrons (oxidise) and thus reduce the ions of less reactive metals.
- In the electrochemical series, metals with more negative reduction potentials are stronger reducing agents and will displace those with less negative (or positive) potentials.
Final Answer:
Mg>Al>Zn>Fe>Cu
Here are the common mistakes students make when tackling this galvanic series / displacement question, along with how to avoid each.
Mistake 1: Confusing the Reactivity Series Order
The Error: Students often misplace Al and Zn, or put Fe before Mg. A common wrong order is: Mg > Al > Zn > Fe > Cu (correct) vs. Mg > Zn > Al > Fe > Cu (incorrect — Al is actually more reactive than Zn in the electrochemical series).
Why it happens: In many everyday contexts (like the reactivity series taught in Class 10), Zn appears more reactive than Al because Al forms a protective oxide layer. However, in displacement reactions from salt solutions (aqueous medium), the standard electrode potential (E∘) is the true guide.
How to avoid:
- Memorise the electrochemical series for these five metals using their standard reduction potentials (E∘):
- Mg: −2.37 V (most reactive)
- Al: −1.66 V
- Zn: −0.76 V
- Fe: −0.44 V
- Cu: +0.34 V (least reactive)
- Trick: Remember the mnemonic "Mighty Al Zebras Fight Copper" (Mg > Al > Zn > Fe > Cu).
- Key rule: A metal with a more negative E∘ will displace a metal with a less negative (or positive) E∘ from its salt solution.
Mistake 2: Forgetting the Displacement Direction
The Error: Students write the order as Cu > Fe > Zn > Al > Mg (the reverse of the correct order).
Why it happens: They confuse "displaces" with "is displaced by." The question asks: "in the order in which they displace each other" — meaning the most reactive metal (which displaces all others) comes first.
How to avoid:
- Read carefully: "Displace each other" means metal A displaces metal B from B's salt. The most reactive metal displaces the most others.
- Use a simple test: If you put Mg metal into a solution of CuSO4, Mg displaces Cu. So Mg is more reactive than Cu. Therefore, Mg comes before Cu in the list.
- Correct order: Mg > Al > Zn > Fe > Cu (most reactive to least reactive).
Mistake 3: Ignoring the Role of the Oxide Layer on Aluminium
The Error: Students think Al is less reactive than Zn because Al doesn't visibly react with water or dilute acids in the lab.
Why it happens: Al has a tough, adherent oxide layer (Al2O3) that passivates it. In displacement reactions from salt solutions, this layer can slow down the reaction, but thermodynamically, Al is still more reactive than Zn.
How to avoid:
- Distinguish between kinetics and thermodynamics: The oxide layer affects rate (how fast), not spontaneity (whether it happens). In a salt solution, the oxide layer may dissolve or be breached, and Al will eventually displace Zn2+.
- Always use the standard electrode potential for the order, not your lab observation of a single reaction.
Mistake 4: Writing the Order as a List Without Justification
The Error: Students just write Mg, Al, Zn, Fe, Cu without showing the reasoning or the displacement reactions.
Why it happens: They memorise the order but don't understand the underlying concept.
How to avoid:
- Show at least one displacement reaction for each pair. For example:
- Mg displaces Al: 3Mg+2Al3+→3Mg2++2Al
- Al displaces Zn: 2Al+3Zn2+→2Al3++3Zn
- Zn displaces Fe: Zn+Fe2+→Zn2++Fe
- Fe displaces Cu: Fe+Cu2+→Fe2++Cu
- Conclusion: Since Mg displaces all others, it is the most reactive. Cu is displaced by all, so it is the least reactive.
Final Correct Answer (Exam-Ready Format)
Correct order: Mg>Al>Zn>Fe>Cu
Reasoning: Based on standard electrode potentials (E∘):
- Mg (−2.37 V) has the most negative E∘, so it is the strongest reducing agent and displaces all others.
- Cu (+0.34 V) has the most positive E∘, so it is the weakest reducing agent and is displaced by all others.
Common mistake to avoid: Do not reverse the order or misplace Al and Zn. Use the electrochemical series, not memory tricks that ignore the oxide layer.
- KCET 2025Set D-41 markMCQQ.Match the following select the correct option for the quantity of electricity, in Cmol−1 required to deposit various metals at cathode List - I a Ag+ b Mg2+ c Al3+ d Ti4+ List - II i 386000Cmol−1 ii 289500Cmol−1 iii 96500Cmol−1 iv 193000Cmol−1 (A) a - ii, b - i, c - iv, d - iii (B) a - iii, b - iv, c - ii, d - i (C) a - iv, b - iii, c - i, d - ii (D) a - i, b - ii, c - iii, d - iv
›Reveal solutionSolution
The charge needed per mole of metal is just n×F, where n is the cation's charge and F=96500Cmol−1 — so simply multiply 96500 by 1,2,3,4.
Step 1 — The governing law.
The cathodic reduction is
Mn++ne−→M
One mole of Mn+ therefore consumes exactly n moles of electrons. Faraday's constant is the charge on one mole of electrons,
F=96500 Cmol−1
so the quantity of electricity required per mole of metal deposited is
Q=nF
Step 2 — Compute for each cation.
- (a) Ag+, n=1: Q=1×96500=96500 Cmol−1 → (iii)
- (b) Mg2+, n=2: Q=2×96500=193000 Cmol−1 → (iv)
- (c) Al3+, n=3: Q=3×96500=289500 Cmol−1 → (ii)
- (d) Ti4+, n=4: Q=4×96500=386000 Cmol−1 → (i)
Step 3 — Assemble the matching.
a−iii,b−iv,c−ii,d−i
This is exactly option (B). Note the neat check: the four List-II values are just 96500 multiplied by 1,4,3,2 in the order printed, and the charge required rises monotonically with the cation's charge — Ag+ (cheapest) to Ti4+ (dearest).
✓Final answerThe correct option is (B) — a - iii, b - iv, c - ii, d - i.
ANSWER: B
- KCET 2024Set B-21 markMCQQ.The transition element (≈5%) present with lanthanoid metal in Misch metal is: (A) Mg (B) Fe (C) Zn (D) Co
›Reveal solutionSolution
Recall the composition of Misch metal: ~95% lanthanoid + ~5% iron, with traces of S, C, Ca and Al.
Step 1 — What Misch metal is.
Misch metal is a commercially important lanthanoid alloy. Its composition is:
- ~95% lanthanoid metal (mostly cerium, with lanthanum, neodymium and praseodymium),
- ~5% iron,
- traces of S, C, Ca and Al.
Step 2 — Identify the transition element.
The question asks specifically for the transition element present at the ~5% level. Screening the options against the d-block:
Option Element Block (A) Mg s-block (alkaline earth) — not a transition metal (B) Fe 3d transition series ✓ (C) Zn 3d series, but d10 in all its compounds — and not the 5% component (D) Co 3d series, but not a component of Misch metal Only Fe is both a transition element and the ~5% component of Misch metal, so it satisfies the question completely.
Step 3 — Why it is worth remembering.
Misch metal's headline use is in cigarette lighter flints and tracer bullets: it is pyrophoric — scraping it throws off sparks. It is also added to steel as a scavenger, because the lanthanoids mop up sulphur and oxygen.
✓Final answerThe correct option is (B) — Fe.
ANSWER: B
- COMEDK 2024Set 2024-A1 markMCQQ.The E∘ values of A.B and C are given. Which element/(s) is/(are) good for coating the surface of iron to prevent corrosion? Given: [EFe2+/Fe0=−0.44 V;EA2+/A0=−2.37 V;EB2+/B0=−0.15 V;EC2+/C0=+0.34 V] (A) Element C only (B) Elements B and C (C) Element B only (D) Element A only
›Reveal solutionSolution
To prevent iron corrosion by coating, the coating metal must be more easily oxidized (more negative reduction potential) than iron, so it acts as a sacrificial anode. Only element A (E∘=−2.37 V) satisfies this, making option (D) correct.
Concept & Intuition
Corrosion of iron (rusting) is an electrochemical process where iron is oxidized:
Fe→Fe2++2e−(E∘=−0.44 V)
If we coat iron with another metal, we want that metal to oxidize instead of iron — it “sacrifices” itself. This happens if the coating metal has a more negative reduction potential than iron, meaning it is a stronger reducing agent (more easily oxidized). A metal with a less negative or positive reduction potential would actually cause iron to corrode faster (it would act as a cathode, forcing iron to be the anode).
Step-by-step reasoning
-
Identify iron’s tendency to oxidize
Iron’s reduction potential is EFe2+/Fe∘=−0.44 V. The more negative this value, the easier it is for the metal to lose electrons (oxidize). So iron itself is moderately prone to oxidation.
-
Compare each candidate metal’s reduction potential
- Element A: EA2+/A∘=−2.37 V — much more negative than iron.
- Element B: EB2+/B∘=−0.15 V — less negative than iron.
- Element C: EC2+/C∘=+0.34 V — positive, meaning it is very hard to oxidize.
-
Determine which metal will oxidize preferentially
For a coating to protect iron, the coating metal must have a more negative reduction potential than iron. That way, when an electrochemical cell forms (e.g., with moisture and oxygen), the coating metal becomes the anode and corrodes, while iron remains the cathode and is protected.
- A (−2.37 V) is more negative than Fe (−0.44 V) → A will protect iron.
- B (−0.15 V) is less negative than Fe → B is harder to oxidize than iron, so iron would corrode first.
- C (+0.34 V) is positive → C is very noble; it would actually accelerate iron corrosion (iron becomes the sacrificial anode).
-
Apply to the multiple-choice options
Only element A qualifies. Options:
- (A) Element C only — incorrect.
- (B) Elements B and C — incorrect.
- (C) Element B only — incorrect.
- (D) Element A only — correct.
Watch outA common mistake is thinking that any metal with a less negative potential than iron will protect it. In reality, only metals with a more negative potential (like zinc, magnesium, or here element A) act as sacrificial anodes. Metals like tin or copper (with less negative or positive potentials) actually promote rusting if the coating is scratched.
TipThink of the reduction potential as a “ladder”: the more negative the value, the higher the metal sits on the reactivity series. A higher (more reactive) metal will sacrifice itself for a lower (less reactive) metal. Iron at −0.44 V is protected only by metals above it (more negative), like A at −2.37 V.
✓Final answerThe correct option is (D).
ANSWER: D
-
- COMEDK 2024Set 2024-E1 markMCQQ.Identify the correct statement regarding corrosion of iron rod left exposed to atmosphere. (A) The reaction occurring at the cathodic area is: O2( g)+2H2O(l)+4e→4OH− (B) The reaction occurring at the cathodic area is: O2( g)+4H+(aq)+4e→2H2O(l);E0=+1.23 V (C) Reaction occurring at anodic area is: 2H2O(l)→O2( g)+4H++4e (D) The overall reaction occurring during the corrosion process is: 2Fe(S)+3/2O2( g)+6H+→2Fe3++3H2O;E0=−1.23 V
›Reveal solutionSolution
The cathodic (reduction) reaction in rusting is O2+4H++4e−→2H2O with E0=+1.23V — statement (B).
Electrochemical mechanism of rusting (NCERT):
- Anode (oxidation): Fe(s)→Fe2++2e−, E(Fe2+/Fe)0=−0.44V.
- Cathode (reduction): in the presence of H+ (from dissolved CO2/water) and atmospheric oxygen, O2(g)+4H+(aq)+4e−→2H2O(l), E0=+1.23V.
- Overall: 2Fe+O2+4H+→2Fe2++2H2O; the Fe2+ is then further oxidised to hydrated Fe2O3 (rust).
Checking the options: (A) gives the neutral/basic oxygen-reduction half-reaction, not the one used in the standard rusting description; (C) wrongly makes water oxidation the anodic reaction (the anode is iron dissolution); (D) gives a wrong overall reaction with an incorrect negative E0 (corrosion is spontaneous, net E0>0). Only (B) is correct.
✓Final answerThe correct option is (B) — cathodic reaction O2(g)+4H+(aq)+4e→2H2O(l);E0=+1.23V
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