CUET UG Chemistry Booster Test - 2 Electrode Potential and Thermodynamics
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QUESTION 1 OF 20
At the electrode-electrolyte interface, metal ions from solution have a tendency to deposit on the metal electrode. What does this process attempt to do to the electrode?
QUESTION 2 OF 20
Match the opposing tendencies at the electrode-electrolyte interface with their corresponding charge outcomes on the electrode at equilibrium.
| List I | List II |
|---|---|
| 1. Metal ions depositing from solution | a. Results in zero net current |
| 2. Metal atoms going into solution as ions | b. Generates electrode potential |
| 3. Equal rates of deposition and dissolution | c. Tries to make electrode positive |
| 4. Overall separation of charges | d. Tries to make electrode negative |
QUESTION 3 OF 20
Arrange the following half-cells in decreasing order of their standard reduction potentials (from highest to lowest) based on their oxidising strength.
1. H⁺(aq)/H₂(g)
2. Li⁺(aq)/Li(s)
3. F₂(g)/F⁻(aq)
4. Cu²⁺(aq)/Cu(s)
QUESTION 4 OF 20
According to modern IUPAC nomenclature conventions, standard reduction potentials are exclusively referred to as:
QUESTION 5 OF 20
What is the standard electrode potential assigned to the standard hydrogen electrode (SHE)?
QUESTION 6 OF 20
Identify the reaction type for the process:
2H⁺(aq) + 2e⁻ → H₂(g) at E° = 0.00 V.
QUESTION 7 OF 20
the electrode potential at any concentration measured with respect to the Standard Hydrogen Electrode can be represented by:
E(Mⁿ⁺/M) = E°(Mⁿ⁺/M) − (RT/nF) ln([M]/[Mⁿ⁺])
However, the concentration or activity of the pure solid metal M is taken as unity. Therefore, the equation simplifies and the solid metal concentration does not explicitly appear in the final expression. Here, R is the gas constant (8.314 J K⁻¹ mol⁻¹), F is the Faraday constant (96487 C mol⁻¹), and T is the absolute temperature in Kelvin.
Question
Based on the Nernst passage, why is the concentration of solid M missing from the final simplified Nernst equation?
QUESTION 8 OF 20
the electrode potential at any concentration measured with respect to the Standard Hydrogen Electrode can be represented by:
E(Mⁿ⁺/M) = E°(Mⁿ⁺/M) − (RT/nF) ln([M]/[Mⁿ⁺])
However, the concentration or activity of the pure solid metal M is taken as unity. Therefore, the equation simplifies and the solid metal concentration does not explicitly appear in the final expression. Here, R is the gas constant (8.314 J K⁻¹ mol⁻¹), F is the Faraday constant (96487 C mol⁻¹), and T is the absolute temperature in Kelvin.
Question
Which unit represents the gas constant R as described in the passage?
QUESTION 9 OF 20
Calculate the standard cell emf of the Daniell cell using the standard electrode potentials of Cu²⁺/Cu (+0.34 V) and Zn²⁺/Zn (−0.76 V).
QUESTION 10 OF 20
The fundamental unit of cell potential difference (emf) is:
QUESTION 11 OF 20
The Nernst equation at 298 K is often written as:
The constant 0.059 arises from simplifying which term?
QUESTION 12 OF 20
Identify the correct statements regarding the Nernst Equation.
Statements:
1. The Nernst equation links cell potential with concentrations of reacting species.
2. Conversion from ln to log involves multiplication by 2.303.
3. The equation applies only to standard-state conditions.
4. The number of electrons transferred is represented by n.
QUESTION 13 OF 20
In the cell:
the concentration of Ag⁺ ions is decreased. What happens to the cell potential?
QUESTION 14 OF 20
Match the following quantities associated with the Nernst equation.
| List I | List II |
|---|---|
| 1. Q | a. Electrons transferred |
| 2. [C]ᶜ[D]ᵈ | b. Reaction quotient |
| 3. [A]ᵃ[B]ᵇ | c. Product concentration term |
| 4. n | d. Reactant concentration term |
QUESTION 15 OF 20
As a galvanic cell operates continuously, the measured cell potential gradually decreases. What is the primary reason?
QUESTION 16 OF 20
A galvanic cell reaches chemical equilibrium after prolonged operation. Which statement correctly describes the cell at equilibrium?
QUESTION 17 OF 20
If the balanced cell reaction is multiplied by 2, what happens to the standard cell potential (E°cell)?
QUESTION 18 OF 20
For the relation
to represent the maximum useful electrical work obtained from a cell, which condition must be satisfied?
QUESTION 19 OF 20
Identify the correct statements regarding the relationship between E°cell and equilibrium constant K.
Statements:
1. A positive E°cell indicates a spontaneous reaction under standard conditions.
2. A positive E°cell generally corresponds to K > 1.
3. At equilibrium, E°cell becomes zero.
4. The relation between E°cell and K is given by at 298 K.
QUESTION 20 OF 20
For the cell reaction
given:
at 298 K, calculate log K.
Test Complete!
Answer Review
1 At the electrode-electrolyte interface, metal ions from solution have a tendency to deposit on the metal electrode. What does this process attempt to do to the electrode?
�� Metal ions from solution gain electrons and deposit on the electrode. �� This process influences charge distribution at the interface. �� It contributes to the development of electrode potential.
At the electrode-electrolyte interface, two opposing processes occur simultaneously. Metal ions present in the solution tend to gain electrons and deposit on the metal surface, while metal atoms from the electrode may lose electrons and enter the solution as ions. When positive metal ions deposit on the electrode, they reduce the excess negative charge present on the metal surface and contribute toward making the electrode relatively positive. NCERT explains that these competing processes continue until equilibrium is established. The resulting separation of charges gives rise to the electrode potential. The tendency of metal ions to deposit on the electrode is therefore associated with making the electrode positively charged. This process is one of the key factors responsible for the development of the potential difference between the electrode and the electrolyte.
- �� Option A → The process does not directly make the electrode neutral.
- �� Option B → Positive ion deposition does not make the electrode negative.
- �� Option D → Deposition is the opposite of dissolution.
Concept Application
- Application
- Analyze the effect of metal ion deposition on the charge of the electrode.
- Final Logic
- Deposition of positive ions tends to make the electrode positively charged.
"Positive Ions Produce Positive Tendency"
2 Match the opposing tendencies at the electrode-electrolyte interface with their corresponding charge outcomes on the electrode at equilibrium.
| List I | List II |
|---|---|
| 1. Metal ions depositing from solution | a. Results in zero net current |
| 2. Metal atoms going into solution as ions | b. Generates electrode potential |
| 3. Equal rates of deposition and dissolution | c. Tries to make electrode positive |
| 4. Overall separation of charges | d. Tries to make electrode negative |
�� Deposition and dissolution occur simultaneously. �� Equilibrium produces no net current. �� Charge separation creates electrode potential.
NCERT explains that at the electrode-electrolyte interface two competing processes occur continuously. Metal ions from solution may deposit on the electrode and tend to make it positively charged. Conversely, metal atoms from the electrode may enter the solution as positive ions, leaving excess electrons behind and tending to make the electrode negatively charged. Eventually, an equilibrium is established where the rates of deposition and dissolution become equal. At this point, there is no net current flow across the interface. The resulting charge separation between the electrode and electrolyte generates the electrode potential. This balance between opposing tendencies is fundamental to understanding the origin of electrode potentials and electrochemical cells. Therefore, the correct matching is 1-c, 2-d, 3-a and 4-b.
- �� Option B → Deposition and dissolution effects are interchanged.
- �� Option C → Charge separation and equilibrium conditions are incorrectly matched.
- �� Option D → Multiple incorrect pairings occur.
NCERT Recall
- Application
- Recall the origin of electrode potential from charge separation at equilibrium.
- Final Logic
- Deposition → Positive tendency, Dissolution → Negative tendency, Equilibrium → No net current.
"Deposit Positive, Dissolve Negative"
3 Arrange the following half-cells in decreasing order of their standard reduction potentials (from highest to lowest) based on their oxidising strength.
1. H⁺(aq)/H₂(g)
2. Li⁺(aq)/Li(s)
3. F₂(g)/F⁻(aq)
4. Cu²⁺(aq)/Cu(s)
�� Higher reduction potential indicates stronger oxidising ability. �� Fluorine has the highest reduction potential. �� Lithium has the lowest reduction potential.
Standard reduction potential measures the tendency of a species to gain electrons and undergo reduction. A higher positive reduction potential indicates a stronger oxidising agent. According to the electrochemical series given in NCERT, fluorine has the highest standard reduction potential of approximately +2.87 V, making it the strongest oxidising agent. Copper has a standard reduction potential of +0.34 V, hydrogen is assigned 0.00 V, and lithium has a highly negative value of about −3.04 V. Therefore, the decreasing order of standard reduction potential is: F₂/F⁻ > Cu²⁺/Cu > H⁺/H₂ > Li⁺/Li Using the numbering given in the question: 3 > 4 > 1 > 2 This sequence also corresponds to decreasing oxidising strength. Such comparisons are essential for predicting spontaneous redox reactions and determining electron flow in electrochemical cells.
- �� Option B → Completely reverses the electrochemical series.
- �� Option C → Places hydrogen above copper incorrectly.
- �� Option D → Places copper above fluorine incorrectly.
NCERT Recall
- Application
- Recall the electrochemical series and compare standard reduction potentials.
- Final Logic
- Higher E° means stronger oxidising agent.
"Fluorine Commands Hydrogen, Lithium"
4 According to modern IUPAC nomenclature conventions, standard reduction potentials are exclusively referred to as:
�� IUPAC follows a standard terminology. �� Reduction potentials are reported uniformly. �� The accepted term is standard electrode potential.
Modern IUPAC recommendations standardize the terminology used in electrochemistry to avoid ambiguity. NCERT follows these conventions and refers to standard reduction potentials as standard electrode potentials. These values are measured relative to the Standard Hydrogen Electrode and are used to compare the tendencies of different species to undergo reduction. Using a single terminology ensures consistency across scientific literature, textbooks and research publications. Standard electrode potentials are tabulated extensively and form the basis of electrochemical calculations, prediction of reaction feasibility and determination of cell emf. Therefore, the accepted IUPAC term is standard electrode potential.
- �� Option A → Oxidation potentials are not the preferred IUPAC terminology.
- �� Option B → This is not the official IUPAC term.
- �� Option C → Though related, it is not the preferred nomenclature.
NCERT Recall
- Application
- Recall the terminology adopted in NCERT and IUPAC recommendations.
- Final Logic
- IUPAC uses the term Standard Electrode Potential.
"IUPAC Prefers Electrode"
5 What is the standard electrode potential assigned to the standard hydrogen electrode (SHE)?
�� The standard hydrogen electrode (SHE) is the reference electrode. �� All standard electrode potentials are measured relative to SHE. �� Its standard electrode potential is assigned a value of 0.00 V.
According to NCERT, the Standard Hydrogen Electrode (SHE) is used as the universal reference electrode for measuring electrode potentials. It consists of a platinum electrode coated with platinum black, immersed in a solution containing hydrogen ions of unit activity, while hydrogen gas is bubbled at a pressure of 1 bar. Since it is impossible to measure the absolute potential of a single electrode, a reference electrode is required. By international convention, the standard electrode potential of the SHE is assigned the value 0.00 V at 298 K. The electrode potentials of all other electrodes are measured relative to this reference. If an electrode has a positive standard reduction potential relative to SHE, it has a greater tendency to undergo reduction than hydrogen ions. Thus, the value assigned to SHE is 0.00 V, making option A correct.
- �� Option B → SHE is not assigned a potential of +1.00 V.
- �� Option C → SHE is not assigned a negative potential.
- �� Option D → Coulomb (C) is a unit of charge, not electrode potential.
NCERT Recall
- Application
- Recall the definition and significance of the standard hydrogen electrode given in NCERT.
- Final Logic
- SHE is the reference electrode and is assigned a standard electrode potential of 0.00 V.
"Hydrogen Starts at Zero."
6 Identify the reaction type for the process:
2H⁺(aq) + 2e⁻ → H₂(g) at E° = 0.00 V.
�� Hydrogen ions gain electrons. �� Gain of electrons is reduction. �� This reaction defines the Standard Hydrogen Electrode.
The reaction 2H⁺(aq) + 2e⁻ → H₂(g) represents the gain of electrons by hydrogen ions. According to NCERT, reduction is defined as the gain of electrons. Since hydrogen ions accept two electrons and are converted into hydrogen gas, the process is a reduction half-reaction. This reaction is extremely important in electrochemistry because it forms the basis of the Standard Hydrogen Electrode (SHE), whose standard electrode potential is assigned a value of 0.00 V. All other standard electrode potentials are measured relative to this electrode. The equation represents only one half of a redox process because oxidation is not shown. Therefore, it is classified as a reduction half-reaction and not as an overall redox reaction.
- �� Option A → Oxidation involves loss of electrons.
- �� Option C → Only one half-reaction is shown.
- �� Option D → No acid-base neutralization occurs.
Concept Application
- Application
- Apply the definition of reduction as gain of electrons.
- Final Logic
- Hydrogen ions gain electrons; therefore, the process is reduction.
"GER = Gain of Electrons is Reduction"
7
the electrode potential at any concentration measured with respect to the Standard Hydrogen Electrode can be represented by:
E(Mⁿ⁺/M) = E°(Mⁿ⁺/M) − (RT/nF) ln([M]/[Mⁿ⁺])
However, the concentration or activity of the pure solid metal M is taken as unity. Therefore, the equation simplifies and the solid metal concentration does not explicitly appear in the final expression. Here, R is the gas constant (8.314 J K⁻¹ mol⁻¹), F is the Faraday constant (96487 C mol⁻¹), and T is the absolute temperature in Kelvin.
Question
Based on the Nernst passage, why is the concentration of solid M missing from the final simplified Nernst equation?
�� Pure solids have constant activity. �� Their activity is taken as unity. �� Hence they do not appear in Q.
The Nernst equation contains the reaction quotient, which includes the activities or concentrations of species participating in the reaction. According to NCERT, the activity of a pure solid is taken as unity. Since the metal M is present as a pure solid in the electrode reaction, its activity remains constant and does not affect the electrode potential. As a result, the term corresponding to the solid metal is omitted from the final form of the Nernst equation. This simplification is commonly used in electrochemistry because the concentration of a pure solid does not change significantly during the reaction. Therefore, the concentration of solid M is absent from the final expression because its activity is taken as unity.
- �� Option A → The metal is not omitted because it dissolves completely.
- �� Option C → The gas constant does not remove concentration terms.
- �� Option D → Solid metals are good conductors of electricity.
NCERT Recall
- Application
- Recall the rule that pure solids have unit activity.
- Final Logic
- Pure solids have activity equal to one and are omitted from Q.
"Pure Solid = One"
8
the electrode potential at any concentration measured with respect to the Standard Hydrogen Electrode can be represented by:
E(Mⁿ⁺/M) = E°(Mⁿ⁺/M) − (RT/nF) ln([M]/[Mⁿ⁺])
However, the concentration or activity of the pure solid metal M is taken as unity. Therefore, the equation simplifies and the solid metal concentration does not explicitly appear in the final expression. Here, R is the gas constant (8.314 J K⁻¹ mol⁻¹), F is the Faraday constant (96487 C mol⁻¹), and T is the absolute temperature in Kelvin.
Question
Which unit represents the gas constant R as described in the passage?
�� R is the universal gas constant. �� It appears in thermodynamics and electrochemistry. �� Its unit contains energy, temperature and mole terms.
The universal gas constant R is one of the fundamental constants used in chemistry and physics. In the Nernst equation, it relates temperature to the energy changes associated with electrochemical processes. NCERT gives the value of R as 8.314 J K⁻¹ mol⁻¹. The unit indicates that R relates energy (joules) to temperature (kelvin) per mole of substance. This constant appears in thermodynamics, gas laws and electrochemistry. Correct identification of its unit is important when deriving the Nernst equation and performing electrochemical calculations. Therefore, the correct unit of the gas constant is J K⁻¹ mol⁻¹.
- �� Option A → Unit of the Faraday constant.
- �� Option B → Unit of potential difference.
- �� Option D → Unit related to molar conductivity.
NCERT Recall
- Application
- Recall the numerical value and unit of the gas constant R.
- Final Logic
- R = 8.314 J K⁻¹ mol⁻¹.
"R Relates Joules, Kelvin and Moles"
9 Calculate the standard cell emf of the Daniell cell using the standard electrode potentials of Cu²⁺/Cu (+0.34 V) and Zn²⁺/Zn (−0.76 V).
�� Use the standard emf equation. �� Cathode potential minus anode potential. �� Daniell cell is spontaneous.
For a galvanic cell, NCERT gives the expression: E°cell = E°cathode − E°anode In the Daniell cell, copper acts as the cathode and zinc acts as the anode. Therefore: E°cell = (+0.34 V) − (−0.76 V) E°cell = 0.34 + 0.76 E°cell = 1.10 V A positive value of cell emf indicates that the reaction is spontaneous under standard conditions. The Daniell cell is one of the most common examples of a galvanic cell and demonstrates the conversion of chemical energy into electrical energy. Therefore, the standard emf of the Daniell cell is 1.10 V.
- �� Option A → Incorrect subtraction.
- �� Option B → Wrong sign and incorrect calculation.
- �� Option C → Cell emf for a spontaneous Daniell cell is positive.
Substitution
- Application
- Substitute the cathode and anode potentials into the emf equation.
- Final Logic
- 1.10 V = 0.34 − (−0.76).
"Cathode Minus Anode"
10 The fundamental unit of cell potential difference (emf) is:
�� Cell emf is a potential difference. �� Potential difference is measured in volts. �� Volt is the SI unit of electric potential.
The electromotive force (emf) of an electrochemical cell is the maximum potential difference between two electrodes when no current is drawn from the cell. Since emf is a form of electrical potential difference, its SI unit is the volt (V). One volt is defined as one joule of energy per coulomb of charge. NCERT consistently expresses electrode potentials, cell potentials and standard reduction potentials in volts. The unit allows comparison of the driving force of different electrochemical reactions and is fundamental to all electrochemical calculations. Therefore, the correct unit of cell potential difference is volt.
- �� Option A → Ampere is the unit of electric current.
- �� Option C → Ohm is the unit of electrical resistance.
- �� Option D → Siemens is the unit of electrical conductance.
NCERT Recall
- Application
- Recall the SI unit used for electrode and cell potentials.
- Final Logic
- Potential difference is measured in volts.
"Voltage Uses Volts"
11 The Nernst equation at 298 K is often written as:
The constant 0.059 arises from simplifying which term?
�� Nernst equation relates cell potential to concentration. �� At 298 K, constants are simplified. �� The value 0.059 comes from mathematical substitution of constants.
The Nernst equation in its general form is: where R is the gas constant, T is the temperature in Kelvin, F is the Faraday constant and Q is the reaction quotient. NCERT converts the natural logarithm (ln) into common logarithm (log₁₀) using the relation: Substituting T = 298 K, R = 8.314 J mol⁻¹ K⁻¹ and F = 96487 C mol⁻¹ gives: Therefore, the Nernst equation becomes: This simplified form is widely used in electrochemistry problems at room temperature. The constant 0.059 is not an independent physical constant but a derived value obtained by combining R, T, F and the conversion factor 2.303. Hence option A is correct according to NCERT.
- �� Option B → Faraday constant alone cannot produce the value 0.059.
- �� Option C → Gas constant alone is 8.314 and does not equal 0.059.
- �� Option D → Equilibrium constant is unrelated to the derivation of 0.059.
NCERT Recall
- Application
- Recall the simplified Nernst equation given in NCERT for 298 K and identify the origin of the constant 0.059.
- Final Logic
- 0.059 is obtained from at 298 K, not from any single constant.
"2.303 × RT/F at 298 = 0.059"
12 Identify the correct statements regarding the Nernst Equation.
Statements:
1. The Nernst equation links cell potential with concentrations of reacting species.
2. Conversion from ln to log involves multiplication by 2.303.
3. The equation applies only to standard-state conditions.
4. The number of electrons transferred is represented by n.
�� Nernst equation connects concentration and potential. �� The term n represents electrons transferred. �� It is applicable to non-standard conditions.
The Nernst equation is one of the most important equations in electrochemistry. According to NCERT, it establishes a relationship between cell potential and the concentrations of reactants and products through the reaction quotient Q. Therefore statement 1 is correct. The equation is originally expressed using natural logarithms, and conversion to common logarithms is achieved using the relation ln x = 2.303 log x; hence statement 2 is correct. The quantity n represents the number of electrons transferred in the balanced redox reaction, making statement 4 correct. Statement 3 is incorrect because the Nernst equation is specifically used to determine electrode and cell potentials under non-standard conditions. Standard-state potentials are represented by E° values. Thus, statements 1, 2 and 4 are correct and statement 3 is incorrect. Therefore option C is the correct answer.
- �� Option A → Statement 3 is incorrect.
- �� Option B → Statement 3 is incorrect and statement 1 is omitted.
- �� Option D → Includes incorrect statement 3.
Concept Application
- Application
- Check each statement against the NCERT definition and use of the Nernst equation.
- Final Logic
- Statements 1, 2 and 4 agree with NCERT; statement 3 does not.
"Potential–Concentration–Electrons" = Nernst
13 In the cell:
the concentration of Ag⁺ ions is decreased. What happens to the cell potential?
�� Ag⁺ ions participate in reduction. �� Lower Ag⁺ concentration affects Q. �� Nernst equation predicts a decrease in Ecell.
For the cell reaction: the reaction quotient is: According to the Nernst equation: When the concentration of Ag⁺ decreases, the denominator of Q becomes smaller. As a result, the value of Q increases. Since log Q increases, the subtraction term becomes larger and the cell potential decreases. This agrees with NCERT's discussion of concentration effects on cell potential. The cathode reaction depends directly on Ag⁺ ions, and reducing their concentration reduces the tendency of silver ions to gain electrons. Consequently, the driving force of the electrochemical reaction becomes weaker and Ecell decreases. Therefore option B is correct.
- �� Option A → A decrease in Ag⁺ concentration does not increase Ecell.
- �� Option C → Cell potential depends on concentration and therefore changes.
- �� Option D → The potential does not instantly become zero merely due to concentration change.
Concept Application
- Application
- Write the reaction quotient and observe how concentration changes affect Q and Ecell.
- Final Logic
- Decrease in Ag⁺ → increase in Q → decrease in Ecell.
"Cathode ion down → Cell voltage down."
14 Match the following quantities associated with the Nernst equation.
| List I | List II |
|---|---|
| 1. Q | a. Electrons transferred |
| 2. [C]ᶜ[D]ᵈ | b. Reaction quotient |
| 3. [A]ᵃ[B]ᵇ | c. Product concentration term |
| 4. n | d. Reactant concentration term |
�� Q represents reaction quotient. �� Product concentrations appear in numerator. �� n denotes electrons transferred.
The Nernst equation contains several important quantities. The reaction quotient Q expresses the ratio of product concentrations to reactant concentrations raised to their stoichiometric powers. Therefore Q corresponds to the reaction quotient. The expression [C]ᶜ[D]ᵈ represents the product concentration term because products appear in the numerator of Q. Similarly, [A]ᵃ[B]ᵇ represents the reactant concentration term because reactants appear in the denominator of Q. The symbol n represents the number of electrons transferred in the balanced redox reaction. These definitions are directly used in NCERT while deriving and applying the Nernst equation. Matching these concepts correctly gives 1-b, 2-c, 3-d and 4-a. Hence option D is correct.
- �� Option A → Incorrectly matches all quantities.
- �� Option B → Incorrectly interchanges Q and concentration terms.
- �� Option C→ Incorrectly assigns n and Q.
NCERT Recall
- Application
- Recall the standard form of the reaction quotient and identify each symbol.
- Final Logic
- Q = reaction quotient, products in numerator, reactants in denominator, n = electrons transferred.
"Q checks Products/Reactants; n counts electrons."
15 As a galvanic cell operates continuously, the measured cell potential gradually decreases. What is the primary reason?
�� Cell reactions alter concentrations. �� Reaction quotient gradually increases. �� Nernst equation predicts a reduction in cell potential.
A galvanic cell generates electrical energy through a spontaneous redox reaction. As the reaction proceeds, reactants are consumed and products are formed. Consequently, reactant ion concentrations decrease while product ion concentrations increase. According to the Nernst equation, the reaction quotient Q continuously changes during cell operation. As Q increases, the value of the term increases, causing the cell potential to decrease. NCERT explains that the cell potential falls gradually until equilibrium is reached. At equilibrium, there is no net tendency for the reaction to proceed and the cell potential becomes zero. Therefore the gradual change in concentration is the fundamental reason for the decrease in cell voltage. This behavior reflects the close relationship between thermodynamics and electrochemistry discussed in the NCERT chapter. Hence option D is correct.
- �� Option A → Standard electrode potentials remain constant at a given temperature.
- �� Option B → Salt bridge function is not the primary reason for the gradual voltage drop.
- �� Option C → Physical shrinking of the cathode is not responsible for the thermodynamic decrease in potential.
Concept Application
- Application
- Apply the Nernst equation and analyze how concentration changes affect Q and Ecell.
- Final Logic
- Reaction progress changes concentrations → Q increases → Ecell decreases.
"Reaction moves forward, voltage moves downward."
16 A galvanic cell reaches chemical equilibrium after prolonged operation. Which statement correctly describes the cell at equilibrium?
�� Equilibrium means no net reaction occurs. �� The reaction quotient becomes equal to the equilibrium constant. �� Cell potential becomes zero at equilibrium.
According to NCERT, the driving force for a galvanic cell is the free energy change associated with the redox reaction. As the cell operates, reactants are consumed and products are formed, causing the reaction quotient Q to increase. Eventually, the system reaches chemical equilibrium where the forward and reverse reactions occur at equal rates. At this stage, there is no net tendency for the reaction to proceed in either direction. The Gibbs free energy change becomes zero and the cell can no longer perform electrical work. Since the cell potential is directly related to the Gibbs free energy change through the relation ΔG = –nFEcell, the cell potential also becomes zero. Therefore, a voltmeter connected across the cell terminals will show no potential difference. This condition is an important consequence of the Nernst equation and demonstrates the relationship between electrochemistry and chemical equilibrium. Hence, option C is correct.
- �� Option A → Current ceases at equilibrium; it is not maximum.
- �� Option B → Reactants remain present at equilibrium and do not become zero.
- �� Option D → Equilibrium does not require an external potential greater than the standard emf.
NCERT Recall
- Application
- Recall the NCERT statement that Ecell = 0 at equilibrium.
- Final Logic
- Equilibrium ⇒ ΔG = 0 ⇒ Ecell = 0.
"Equilibrium = No Push = No Voltage."
17 If the balanced cell reaction is multiplied by 2, what happens to the standard cell potential (E°cell)?
�� E°cell is an intensive property. �� Stoichiometric coefficients do not affect E°cell. �� Only ΔG changes proportionally.
The standard cell potential is an intensive property and does not depend on the amount of substance involved in the reaction. According to NCERT, when a balanced electrochemical reaction is multiplied by any factor, the number of electrons transferred and the Gibbs free energy change are multiplied by the same factor. Since the relation between them is: both ΔG° and n increase proportionally. As a result, the value of E°cell remains unchanged. This behavior is similar to temperature, density and pressure, which are also intensive properties. For example, if a reaction with E°cell = 1.10 V is doubled, the value of E°cell remains 1.10 V and does not become 2.20 V. Understanding this principle is essential when calculating thermodynamic quantities and equilibrium constants using electrochemical data. Therefore, option C is correct.
- �� Option A → E°cell does not double when coefficients are doubled.
- �� Option B → E°cell does not decrease with coefficient changes.
- �� Option D → E°cell is not multiplied by four.
Concept Application
- Application
- Identify whether the quantity is intensive or extensive.
- Final Logic
- E°cell is intensive; therefore, changing coefficients does not affect its value.
"Double Reaction, Same Voltage."
18 For the relation
to represent the maximum useful electrical work obtained from a cell, which condition must be satisfied?
�� Maximum work is obtained only under reversible conditions. �� Irreversible processes lose energy. �� NCERT derives the relation using reversible cell operation.
The Gibbs free energy change represents the maximum useful work obtainable from a chemical process under specified conditions. In electrochemistry, NCERT explains that the relation: is valid when electrical energy is obtained reversibly from the cell. Under reversible conditions, the system remains extremely close to equilibrium at every stage, ensuring that the maximum amount of useful electrical work is extracted. If the process occurs irreversibly, some energy is dissipated as heat or lost through other inefficiencies, resulting in less useful work than predicted by ΔG. Therefore, reversible transfer of charge is essential for establishing the exact thermodynamic relationship between Gibbs free energy and cell potential. This principle forms the basis for connecting electrochemical measurements with thermodynamic quantities. Hence, option A is correct.
- �� Option B → The relation is valid at ordinary temperatures and not only at 0 K.
- �� Option C → The equation applies to spontaneous cell reactions.
- �� Option D → Variable pressure is not the required condition.
NCERT Recall
- Application
- Recall the thermodynamic derivation given in NCERT.
- Final Logic
- Maximum useful work is obtained only from a reversible process.
"Maximum Work = Reversible Work."
19 Identify the correct statements regarding the relationship between E°cell and equilibrium constant K.
Statements:
1. A positive E°cell indicates a spontaneous reaction under standard conditions.
2. A positive E°cell generally corresponds to K > 1.
3. At equilibrium, E°cell becomes zero.
4. The relation between E°cell and K is given by at 298 K.
�� Positive E°cell implies spontaneity. �� Larger K values favor products. �� E°cell and K are directly related.
NCERT establishes the relationship between standard cell potential and the equilibrium constant using thermodynamic principles. A positive value of E°cell indicates that the cell reaction is spontaneous under standard conditions, making statement 1 correct. Since spontaneous reactions favor product formation, the equilibrium constant K is generally greater than 1, making statement 2 correct. At 298 K, the relation is: which makes statement 4 correct. Statement 3 is incorrect because E°cell is a standard-state quantity and does not become zero at equilibrium. Instead, the actual cell potential Ecell becomes zero when equilibrium is reached. This distinction between E°cell and Ecell is emphasized in NCERT and is frequently tested in examinations. Therefore, statements 1, 2 and 4 are correct, making option D the correct answer.
- �� Option A → Statement 3 is incorrect.
- �� Option B → Statement 3 is incorrect and statement 1 is omitted.
- �� Option C → Includes incorrect statement 3.
Concept Application
- Application
- Differentiate between E°cell and Ecell and apply the NCERT relation connecting E°cell and K.
- Final Logic
- Positive E°cell ⇒ K > 1 and .
"Positive Voltage, Products Prevail."
20 For the cell reaction
given:
at 298 K, calculate log K.
�� Use the relation between E°cell and K. �� Substitute n = 2. �� Calculate log K directly.
According to NCERT, the relationship between standard cell potential and equilibrium constant at 298 K is: For the given reaction: the number of electrons transferred is: Substituting the given values: Thus, the equilibrium constant is extremely large, indicating that the reaction strongly favors product formation under standard conditions. This result is consistent with the positive standard cell potential and the spontaneous nature of the reaction. Therefore, the correct answer is option B.
- �� Option A → Calculation gives 15.6, not 31.2.
- �� Option C → Result is underestimated by a factor of two.
- �� Option D → Does not satisfy the NCERT equation.
Substitution
- Application
- Substitute the numerical values directly into the NCERT equation relating E°cell and K.
- Final Logic
"log K = nE°/0.059"
