NCERT Notes for Class 12 Chapter 2 Electrochemistry
These electrochemistry class 12 ncert notes cover a brief outline of topics such as electrochemical cells, Nernst equation, the Gibbs energy of cell reaction, conductivity, Kohlrausch law and its applications, electrolysis, etc. These notes are the best resource for quick revision, also they help build a clear understanding of fundamental principles and their real-life applications, such as batteries and corrosion. Detailed notes of this chapter are given below.
Conductance of Electrolytic Solutions;
Conductance:
Conductance is the measure of the ease with which current flows through a conductor.
The inverse of resistance, R, is called conductance, G:
$G=1 / R$
where ($R=\rho l / A$)
$\mathrm{G}=\mathrm{A} / \mathrm{\rho l}$
G = KA/l
Where R is resistance, l is length, A is an area of cross-section, ρ (rho) is resistivity, and κ(kappa) is conductivity.
Conductivity:
The inverse of resistivity is called conductivity. The SI units of conductivity are $\mathrm{S} \mathrm{m}^{-1}$, but quite often, κ is expressed in $\mathrm{S} \mathrm{cm}^{-1}$.
κ = 1/ρ
The conductivity of a material in $\mathrm{S} \mathrm{m}^{-1}$ is its conductance when it is 1 m long and its area of cross-section is $1 \mathrm{~m}^2$. It may be noted that 1 $\mathrm{S} \mathrm{cm}^{-1}$.
Molar conductivity:
Molar Conductivity is described as the conducting power produced by the ions by dissolving one mole of electrolyte in a solvent.
Molar conductivity =$\Lambda _{m}=\frac{\kappa }{C}$
Conductivity and molar conductivity-
m= κ×1000/M
Equivalent conductivity-
Equivalent conductivity is defined as the conductivity power of combining ions formed by the dissolution of an electrolyte of one gram equivalent in a solution.
e= κ×1000/Ceq
Measurement of the Conductivity of Ionic Solutions:
We know that accurate measurement of an unknown resistance can be performed on a Wheatstone bridge.
Wheatstone bridge:

It consists of two resistors, R1 and R3, a variable resistor, R2, and the unknown resistor, R4. The Wheatstone bridge is fed by an oscillator $\varepsilon$ (a source of a.c. power). G is a suitable detector (an electronic device, such as a galvanometer), and the bridge is balanced when no current passes through the detector. Under these conditions:
Unknwon resistance $R_{4}=\frac{R_{2}R_{3}}{R_{1}}$
Once the cell constant and the resistance of the solution in the cell are determined, the conductivity of the solution is given by the equation:
$\kappa$ = cell constant/R =G*/R
Variation of conductivity and molar conductivity with concentration:
Electrolytic conductance decreases with an increase in concentration or increases with an increase in dilution.
Molar conductivity increases with dilution:
The equation of Debye-Huckel-Onsager shows the variation of molar conductivity along with concentration for strong electrolytes.
For strong electrolytes: For strong electrolytes, $\Lambda _{m}$ increases slowly with dilution and can be represented by the equation:
$\Lambda _{m}=\Lambda ^{^{\circ}}_{m} - Ac^{1/2}$
Variation of molar conductivity with concentration for weak electrolytes:
Molar conductivity of weak electrolytes cannot be found for weak electrolytes because the dissociation of weak electrolytes is much lower compared to strong electrolytes.
For weak electrolytes, molar conductivity at infinite dilution can be found using Kohlrausch law.
At any concentration c, if α is the degree of dissociation, then it can be approximated by the ratio of molar conductivity $\Lambda _{m}$ at the concentration c to the limiting molar conductivity $\Lambda ^{^{\circ}}_{m}$. Thus we have:
α = $\Lambda _{m}$/ $\Lambda ^{^{\circ}}_{m}$
Kohlrausch’s Law:
At infinite dilution when ions are completely dissociated, every ion makes its unique contribution to the molar conductivity of the electrolyte, irrespective of the nature of the other ion with which it is associated. Students can also refer to ncert class 12 chemistry chapter 2 electrochemistry notes for practicing questions related to these topics.
Applications of
Kohlrausch's Law -
1. Calculation of molar conductance at infinite dilution for weak electrolytes
2. The degree of dissociation of weak electrolytes is calculated as
α = $\Lambda _{m}$/ $\Lambda ^{^{\circ}}_{m}$
3. Calculation of the dissociation constant of weak electrolytes.
$K_{a}=\frac{C\alpha^2}{1-\alpha }$
4. Calculation of the solubility of sparingly soluble salts.
solubility= κ×1000
Electrochemical Cells:
Electrochemical cells are devices that convert chemical energy into electrical energy or vice versa through redox reactions. Students can also refer to NCERT Solutions for Class 12 Chapter 2 Electrochemistry to practise and solve questions from these topics effectively.
Galvanic cells:
Converts the chemical energy of a spontaneous reaction into electrical energy.
Two half cells -
$\mathrm{Cu}^{+2}+2 \mathrm{e}^{-} \rightarrow \mathrm{Cu}_{(\mathrm{s})}($ reduction half cell $)$
$\mathrm{Zn}_{(\mathrm{s})} \rightarrow \mathrm{Zn}^{2+}+2 \mathrm{e}^{-}$(oxidation half cell)
Overall cell reaction-
$\mathrm{Zn}_{(\mathrm{s})}+\mathrm{Cu}^{+2}(\mathrm{aq}) \rightarrow \mathrm{Zn}^{2+}{ }_{(\mathrm{aq})}+\mathrm{Cu}_{(\mathrm{s})}$
Cell potential-
The Potential difference between two electrodes of a
Galvanic Cell is called cell potential.
Measurement of Electrode Potential: EMF (Electromotive Force):
Emf Of Cell is the potential difference between the anode and the cathode when no current is drawn through the cell.
$E_{\text {cell }}=E_{\text {right }}-E_{\text {left }}$
Feasibility of a reaction-
$E_{\text {cell }}=E_{\text {right }}-E_{\text {left }}$
Reduction Half-$2 \mathrm{Ag}^{+}(a q)+2 e^{-} \rightarrow 2 \mathrm{Ag}(s)$
Oxidation Half-$\mathrm{Cu}(s) \rightarrow \mathrm{Cu}^{2+}(a q)+2 e^{-}$
For the above reaction, the reaction is feasible if
Ecell =$\mathrm{E}_{\mathrm{Ag}^{+} / \mathrm{Ag}}$ - $\mathrm{E}_{\mathrm{Cu}^{+2} / \mathrm{Cu}}$ is positive.
SHE (
Standard Hydrogen Electrode) is assigned a zero potential to determine the potential of individual half-cells.
It is denoted by $\mathrm{Pt}_{(\mathrm{s})}\left|\mathrm{H}_{2(\mathrm{~g})}\right| \mathrm{H}^{+}{ }_{(\mathrm{aq})}$
Nernst equation:
For reaction-
$M^{n+}+n e^{-} \longrightarrow M$
$E_{M^{n+} / M}=E_{M^{n+} / M}^{\circ}-\frac{2.303 R T}{n F} \log \frac{1}{\left[M^{n+}\right]}$
$E_{M^{n+} / M}=E_{M^{n+} / M}^{\circ}-\frac{0.0591}{n} \log \left[\frac{1}{M^{n+}}\right]$
Applications of the Nernst equation-
1. Determining the cell potential using the Nernst equation-
Equilibrium Constant from Nernst Equation:
For a chemical reaction-
aA+bB→cC+dD
$E_{\text {cell }}=E_0$ cell $-(R T / n F) \ln (Q)$
$
E_{\text {cell }}=E_{\text {cell }}^{\circ}-\frac{0.0591}{n} \log \left(\frac{[C]^c[D]^d}{[A]^a[B]^b}\right)
$
This is the Nernst equation at 298 K, where:
$E_{\text {cell }}$ is the cell potential under non-standard conditions
$E_{\text {cell }}^{\circ}$ is the standard cell potential
$n$ is the number of moles of electrons transferred
$[A],[B],[C],[D]$ are concentrations of the respective species
$a, b, c, d$ are the stoichiometric coefficients in the balanced redox equation.
2. Determination of the concentration of a solution of a half-cell
Using the
Nernst Equation, the concentration of the unknown species can be found.
3. To find the equilibrium constant using the Nernst equation-
At equilibrium, the Nernst equation takes the form of –
$\mathrm{E}^{\circ}$ cell=2.303 (RT/nF) $\log (\mathrm{K})$
Electrochemical Cell and Gibbs Energy of the Reaction:
$\Delta_{\mathrm{r}} \mathrm{G}=-\mathrm{nFEcell}$
This equation can help to predict the feasibility of the reaction.
Electrolysis- The process in which chemical changes take place due to the passage of current.
Faraday’s Law of electrolysis:
There are two
Faraday’s Laws Of Electrolysis, Faraday’s first law of electrolysis says that the quantity of substance deposited at the electrode is in direct proportion to the amount the electricity passed through the solution.
$w \propto Z Q$
where w is the gram of substance deposited on passing Q coulombs of electricity if a current of 1 ampere is passed for t seconds.
Faraday’s second law of electrolysis- It says that when an equal amount of electricity is passed through different solutions lined up in series, the mass of the substance deposited at the electrodes is in direct proportion to the equivalent weight. Students can also download these electrochemistry class 12 ncert notes pdf to study offline anytime and anywhere.
Weight of Cu deposited = Weight of Ag deposited
= Eq. wt. of Cu = Eq. wt. of Ag
Batteries:
Primary batteries
1. Dry cells- Found in torches, flashlights, calculators, tape recorders, and many other devices.
Reactions occurring at the electrode are-
Anode
$\mathrm{Zn} \rightarrow \mathrm{Zn}^{+2}+2 \mathrm{e}^{-}$
Cathode
$2 \mathrm{NH}_4^{+}(\mathrm{aq})+2 \mathrm{MnO}_2+2 \mathrm{e}^{-} \rightarrow \mathrm{Zn}^{+2}+2 \mathrm{MnOOH}+2 \mathrm{NH}_3$
Overall-
$\mathrm{Zn}+2 \mathrm{NH}_4^{+}(\mathrm{aq})+2 \mathrm{MnO}_2+\mathrm{Zn}^{+2}+2 \mathrm{MnOOH}+2 \mathrm{NH}_3$
2. Mercury cell-
Found in electrical circuits.
Reactions occurring at the electrodes are-
Anode-
$\mathrm{ZnHg}+2 \mathrm{OH}^{-} \rightarrow \mathrm{ZnO}+\mathrm{H}_2 \mathrm{O}+2 \mathrm{e}^{-}$
Cathode-
$\mathrm{HgO}_{(\mathrm{s})}+\mathrm{H}_2 \mathrm{O}+2 \mathrm{e}^{-} \rightarrow \mathrm{Hg}+2 \mathrm{OH}^{-}$
Overall-
$\mathrm{ZnHg}+\mathrm{HgO} \rightarrow \mathrm{ZnO}+2 \mathrm{OH}^{-}$
Secondary batteries:
1. Lead storage batteries-
Battery used in automobiles.
Reactions taking place at electrodes-
Anode-
$\mathrm{PbS}+\mathrm{SO}_4{ }^{2-} \rightarrow \mathrm{PbSO}_4+2 \mathrm{e}^{-}$
Cathode-
$\mathrm{PbO}_2(\mathrm{~s})+\mathrm{SO}_4^{2-}+4 \mathrm{H}^{+}+2 \mathrm{e}^{-} \rightarrow \mathrm{PbSO}_4+2 \mathrm{H}_2 \mathrm{O}$
Overall-
$\mathrm{Pb}+\mathrm{PbO}_2+2 \mathrm{H}_2 \mathrm{SO}_4 \rightarrow 2 \mathrm{PbSO}_4+2 \mathrm{H}_2 \mathrm{O}$
2. Nickel-cadmium storage cell-
Has a longer life than the lead storage battery.
Reactions occurring at electrodes-
Anode-
$\mathrm{Cd}+2 \mathrm{OH}^{-} \rightarrow \mathrm{CdO}+\mathrm{H}_2 \mathrm{O}+2 \mathrm{e}^{-}$
Cathode−
$2 \mathrm{Ni}(\mathrm{OH})_3+2 \mathrm{e}^{-} \rightarrow 2 \mathrm{Ni}(\mathrm{OH})_2+2 \mathrm{OH}^{-}$
Overall-
$\mathrm{Cd}+2 \mathrm{Ni}(\mathrm{OH})_3 \rightarrow \mathrm{CdO}+2 \mathrm{Ni}(\mathrm{OH})_2+\mathrm{H}_2 \mathrm{O}$
Fuel Cells-
- Features
- Reactants are supplied continuously.
- The energy of Combustion of fuels such as H2, CO, CH4, etc. is converted to electrical energy.
- Reactions taking place at electrodes-
Anode-
$2\left[\mathrm{H}_2+2 \mathrm{OH}^{-}(\mathrm{aq}) \rightarrow 2 \mathrm{H}_2 \mathrm{O}+2 \mathrm{e}^{-}\right]$
Cathode-
$\mathrm{O}_2+2 \mathrm{H}_2 \mathrm{O}+4 \mathrm{e}^{-} \rightarrow 4 \mathrm{OH}^{-}(\mathrm{aq})$
Overall-
$2 \mathrm{H}_{2(\mathrm{~g})}+\mathrm{O}_2 \rightarrow 2 \mathrm{H}_2 \mathrm{O}$
Corrosion:
Deterioration of metal over time due to its reaction with air and water.
Except gold, platinum, and palladium all other metals undergo corrosion.
Rusting of iron-
At anode-
$\left[\mathrm{Fe} \rightarrow \mathrm{Fe}^{2+}{ }_{(\mathrm{aq})}+2 \mathrm{e}^{-}\right] \times 2$
At cathode-
$4 \mathrm{H}^{+}+\mathrm{O}_2+4 \mathrm{e}^{-} \rightarrow 2 \mathrm{H}_2 \mathrm{O}$
Overall reaction-
$2 \mathrm{Fe}+4 \mathrm{H}^{+}+\mathrm{O}_2 \rightarrow 2 \mathrm{Fe}^{+2}{ }_{(\mathrm{aq})}+2 \mathrm{H}_2 \mathrm{O}$
Prevention of corrosion-
- Barrier protection
- Sacrificial protection
- electrical protection
NCERT Chapter 2 Electrochemistry Previous Year Questions and Answers
Given below previous years to help you understand important concepts and exam trends. Practising these will improve your accuracy. To understand these concepts better students can refer class 12 chemistry chapter 2 electrochemistry notes.
Question 1. The molar conductance of an infinitely dilute solution of ammonium chloride was found to be $185 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^{-1}$ and the ionic conductance of hydroxyl and chloride ions are 170 and $70 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^1$, respectively. If molar conductance of 0.02 M solution of ammonium hydroxide is $85.5 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^{-1}$, its degree of dissociation is given by $\mathrm{x} \times 10^{-1}$. The value of $x$ is _______ (Nearest integer)
(1) 3
(2) 9
(3) 4
(4) 10
Answer:
$\begin{aligned}
& \lambda_{\mathrm{m}}^{\prime \prime} \text { of } \mathrm{NH}_4 \mathrm{Cl}=185 \\
& \left(\lambda_{\mathrm{m}}^{\circ}\right)_{\mathrm{NH}_4}+\left(\lambda_{\mathrm{m}}^{\circ}\right)_{\mathrm{Cl}^{-}}=185 \\
& \left(\lambda_{\mathrm{m}}^{\circ}\right)_{\mathrm{NH}_4}=185-70=115 \mathrm{Scm}^2 \mathrm{~mol}^{-1} \\
& \left(\lambda_{\mathrm{m}}^{\circ}\right)_{\mathrm{NH}_4 \mathrm{OH}}=\left(\lambda_{\mathrm{m}}^{\circ}\right)_{\mathrm{NH}_4^{\circ}}+\left(\lambda_{\mathrm{m}}^{\circ}\right)_{\mathrm{OH}^{-}} \\
& =115+170 \\
& \left(\lambda_{\mathrm{m}}^0\right)_{\mathrm{NH}_4 \mathrm{OH}}=285 \mathrm{Scm}^2 \mathrm{~mol}^{-1} \\
& \text { degree of dissociation }=\frac{\left(\lambda_{\mathrm{m}}\right)_{\mathrm{NH}_4 \mathrm{OH}}}{\left(\lambda_{\mathrm{m}}^{\circ}\right)_{\mathrm{NH}_4 \mathrm{OH}}} \\
& =\frac{85.5}{285} \\
& =0.3 \\
& =3 \times 10^{-1}
\end{aligned}$
Hence, the answer is option (1).
Question 2: Given below are two statements :
1 M aqueous solution of each of $\mathrm{Cu}\left(\mathrm{NO}_3\right)_2$, $\mathrm{AgNO}_3, \mathrm{Hg}_2\left(\mathrm{NO}_3\right)_2 ; \mathrm{Mg}\left(\mathrm{NO}_3\right)_2$ are electrolysed using inert electrodes,
Given : $\mathrm{E}_{\mathrm{Ag}^* / \mathrm{Ag}}^0=0.80 \mathrm{~V}, \mathrm{E}_{\mathrm{Hg}_2^{2+} / \mathrm{Hg}}^0=0.79 \mathrm{~V}$, $\mathrm{E}_{\mathrm{Cu}^{2+} / \mathrm{Cu}}^0=0.24 \mathrm{~V}$ and $\mathrm{E}_{\mathrm{Mg}^{2+} / \mathrm{Mg}}^0=-2.37 \mathrm{~V}$
Statement (I) : With increasing voltage, the sequence of deposition of metals on the cathode will be $\mathrm{Ag}, \mathrm{Hg}$ and Cu
Statement (II) : Magnesium will not be deposited at cathode instead oxygen gas will be evolved at the cathode.
In the light of the above statement, choose the most appropriate answer from the options given below
(1) Both statement I and statement II are incorrect
(2) Statement I is correct but statement II is incorrect
(3) Both statement I and statement II are correct
(4) Statement I is incorrect but statement II is correct
Answer:
We are electrolyzing 1 M aqueous solutions of the following nitrates using inert electrodes:
-
$\mathrm{Cu}\left(\mathrm{NO}_3\right)_2$
-
$\mathrm{AgNO}_3$
-
$\mathrm{Hg}_2\left(\mathrm{NO}_3\right)_2$
-
$\mathrm{Mg}\left(\mathrm{NO}_3\right)_2$
At the cathode, reduction occurs. So we must look at the standard reduction potentials (E°) for the metal cations.
From the electrochemical series, we can see that,
-
In electrolysis, the ion with the highest E° gets reduced (i.e., deposited) first at the cathode.
-
So as the voltage increases, the cations get deposited in order of decreasing E°.
Thus, the expected order of deposition at the cathode is:
Ag>Hg>Cu
So, Statement I: "With increasing voltage, the sequence of deposition of metals on the cathode will be Ag, Hg, and Cu" is correct.
Let’s analyze the possibility of Mg²⁺ getting reduced:
$2 \mathrm{H}_2 \mathrm{O}+2 e^{-}->\mathrm{H}_2+2 \mathrm{OH}^{-} \quad \mathrm{E}^{\circ}=-0.83 \mathrm{~V}$
So, Mg²⁺ is not deposited — instead, hydrogen gas is evolved at the cathode.
But Statement II says:
"Magnesium will not be deposited at the cathode instead oxygen gas will be evolved at the cathode", is incorrect because oxygen is evolved at the anode, not at the cathode.
At the cathode, hydrogen gas evolves if Mg is not deposited.
Hence, the correct answer is option (2).
Question 3. Given below are two statements :
Statement I : Mohr's salt is composed of only three types of ions-ferrous, ammonium, and sulphate.
Statement II : If the molar conductance at infinite dilution of ferrous, ammonium and sulphate ions are $\mathrm{x}_1, \mathrm{x}_2$ and $\mathrm{x}_3 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^{-1}$, respectively then the molar conductance for Mohr's salt solution at infinite dilution would be given by $\mathrm{x}_1+\mathrm{x}_2+2 \mathrm{x}_3$
In the light of the given statements, choose the correct answer from the options given below :
(1) Both statements I and Statement II are false
(2) Statement I is false but Statement II is true
(3) Statement I is true but Statement II are false
(4) Both statements I and Statement II are true
Answer:
Mohr's salt : $\mathrm{FeSO}_4 \cdot\left(\mathrm{NH}_4\right)_2 \mathrm{SO}_4 \cdot 6 \mathrm{H}_2 \mathrm{O}$
Mohr's salt dissociates into one Fe ion, two ammonium ions and two sulphate ions. Therefore, using Kohlrausch's law we get
$\lambda_{\mathrm{m}}^*(\text { Mohr's salt })=\mathrm{x}_1+2 \mathrm{x}_2+2 \mathrm{x}_3$
Hence, the correct answer is option (3).
Question 4. The correct order of limiting molar conductivity for cations in water at 298 K is
(1) $\mathrm{H}^{+}>\mathrm{Na}^{+}>\mathrm{K}^{+}>\mathrm{Ca}^{2+}>\mathrm{Mg}^{2+}$
(2) $\mathrm{H}^{+}>\mathrm{Ca}^{2+}>\mathrm{Mg}^{2+}>\mathrm{K}^{+}>\mathrm{Na}^{+}$
(3) $\mathrm{Mg}^{2+}>\mathrm{H}^{+}>\mathrm{Ca}^{2+}>\mathrm{K}^{+}>\mathrm{Na}^{+}$
(4) $\mathrm{H}^{+}>\mathrm{Na}^{+}>\mathrm{Ca}^{2+}>\mathrm{Mg}^{2+}>\mathrm{K}^{+}$
Answer:
The limiting molar conductivities of ions are important in determining how well they conduct electricity in solution. Here are the values for some common cations at 298 K :
$\mathrm{H}^{+}: 349.8 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^{-1}$
$\mathrm{Na}^{+}: 50.11 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^{-1}$
$\mathbf{K}^{+}: 73.52 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^{-1}$
$\mathbf{C a}^{\mathbf{2 +}}: 119 \mathrm{~S} \mathrm{~cm}^2 \mathrm{~mol}^{-\mathbf{1}}$
$\mathbf{M g}^{\mathbf{2 +}}: \mathbf{1 0 6 . 1 2} \mathrm{S} \mathrm{cm}^{\mathbf{2}} \mathrm{mol}^{-\mathbf{1}}$
Therefore correct order of limiting molar conductivity of cations will be -$\{\mathrm{H}^{+}>\mathrm{Ca}^{+2}>\mathrm{Mg}^{+2}>\mathrm{K}^{+}>\mathrm{Na}^{+}$}
Hence, the correct answer is option (2).
Question 5. $\mathrm{O}_2$ gas will be evolved as a product of electrolysis of:
(A) an aqueous solution of $\mathrm{AgNO}_3$ using silver electrodes.
(B) an aqueous solution of $\mathrm{AgNO}_3$ using platinum electrodes.
(C) a dilute solution of $\mathrm{H}_2 \mathrm{SO}_4$ using platinum electrodes.
(D) a high concentration solution of $\mathrm{H}_2 \mathrm{SO}_4$ using platinum electrodes.
Choose the correct answer from the options given below :
(1) (B) and (C) only
(2) (A) and (D) only
(3) (B) and (D) only
(4) (A) and (C) only
Answer:
(A) An aqueous solution of $\mathrm{AgNO}_3$ using silver electrodes.
Cathode - Reduction - $A g_{(a q)}^{+}+e^{-} \rightarrow A g(s)$
Anode - Oxidation - $A g(s) \rightarrow A g_{(a q)}^{+}+e^{-}$
Solid silver will be deposited at the cathode. Solid anode (silver) will dissolve, releasing silver ions into the solution.
So, there is no formation of $\mathrm{O}_2$ gas in this electrolysis.
(B) An aqueous solution of $\mathrm{AgNO}_3$ using platinum electrodes.
Cathode - Reduction - $A g_{(a q)}^{+}+e^{-} \rightarrow A g(s)$
Anode - Oxidation - $2 \mathrm{H}_2 \mathrm{O} \rightarrow 4 \mathrm{H}^{+}+\mathrm{O}_2+4 e^{-}$
When platinum electrodes are used, $\mathrm{Ag}^{+}$from solution is reduced and deposited at cathode whereas $\mathrm{O}_2$ is produced at the anode.
(C) A dilute soution of $\mathrm{H}_2 \mathrm{SO}_4$ using platinum electrodes.
Cathode - Reduction - $2 \mathrm{H}^{+}+2 e^{-} \rightarrow \mathrm{H}_2$
Anode - Oxidation - $2 \mathrm{H}_2 \mathrm{O} \rightarrow \mathrm{O}_2+4 \mathrm{H}^{+}+4 e^{-}$
$\mathrm{H}_2$ gas is produded at the cathode and $\mathrm{O}_2$ gas is produced at the anode.
(D) a high concentration solution of $\mathrm{H}_2 \mathrm{SO}_4$ using platinum electrodes.
$\mathrm{O}_2$ gas is not formed in this case.
Cathode - Reduction - The substance formed is $\mathrm{H}_2$ gas.
Anode - Oxidation - The substance formed is not $\mathrm{O}_2$ gas.
So, statements (B) and (C) are correct.
Hence, the correct answer is option (1).
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