The Gibbs’ energy for the decomposition of ${ Al }_{ 2 }{ O }_{ 3 }$ at ${ 500 }^{ \circ }{ C }$ is as follows:
${ 2\div 3Al }_{ 2 }{ O }_{ 3 }{ \rightarrow 4\div 3Al+O }_{ 2 }{ ;\Delta G\circ =+960kJ/mol }$
The potential difference needed for the electrolytic reduction of aluminium oxide ${ Al }_{ 2 }{ O }_{ 3 }$ at ${ 500 }^{ \circ }{ C }$ is at least:
(A) ${ 3.0V }$
(B) ${ 2.5V }$
(C) ${ 5.0V }$
(D) ${ 4.5V }$
Answer
249.9k+ views
Hint:In thermodynamics, the Gibbs free energy is a thermodynamic potential that measures the "useful" or process-initiating work obtainable from an isothermal, isobaric thermodynamic system.
Complete step by step solution:
> The relationship between the Gibbs’ free energy change and the cell potential is given below:
${ \Delta G }^{ \circ }{ =-nFE }^{ \circ }$..........(1)
where, ${ \Delta G }^{ \circ }$ = Gibbs’ free energy change
n = number of electrons transferred
F = Faraday’s constant
${ E }^{ \circ }$ = Electrode potential
It is given that,
${ \Delta G\circ =+960kJ/mol }$ = ${ 960\times 10 }^{ 3 }{ J }mol^{ -1 }$
F = ${ 96500 }$
${ 2\div 3Al }_{ 2 }{ O }_{ 3 }{ \rightarrow 4\div 3Al+O }_{ 2 }$
Here, the value of n = ${ 4 }$
Now, put the values in the equation 1, we get
$ { 960\times 10 }^{ 3 }{ J }mol^{ -1 }= { =\quad -4\times 96500\times E }^{ \circ }$
${ E }^{ \circ }{ =\quad -960000\div 4\times 96500 }$
${ E }^{ \circ }= { =\quad -960000\div 386000 }$
${ E }^{ \circ } = { -2.48V }$
So, difference = ${ 2.5V }$.
Hence, The potential difference needed for the electrolytic reduction of aluminium oxide ${ Al }_{ 2 }{ O }_{ 3 }$ at ${ 500 }^{ \circ }{ C }$ is at least ${ 2.5V }$.
The correct option is B.
> The metals present at the top of the reactivity series such as sodium and potassium can't be reduced using coke, therefore bypassing electric current through their molten salts they are reduced such a process to get metal from its metallic oxide is called Electrolytic Reduction.
> In the spontaneous process, the ${ \Delta G }$ ( free energy change ) must be a negative value.
Note: The possibility to make a mistake is that you have to convert Gibbs’ free energy in J/mol to kJ/mol. Also, the value of electrons transferred in this reaction is ${ 4 }$.
Complete step by step solution:
> The relationship between the Gibbs’ free energy change and the cell potential is given below:
${ \Delta G }^{ \circ }{ =-nFE }^{ \circ }$..........(1)
where, ${ \Delta G }^{ \circ }$ = Gibbs’ free energy change
n = number of electrons transferred
F = Faraday’s constant
${ E }^{ \circ }$ = Electrode potential
It is given that,
${ \Delta G\circ =+960kJ/mol }$ = ${ 960\times 10 }^{ 3 }{ J }mol^{ -1 }$
F = ${ 96500 }$
${ 2\div 3Al }_{ 2 }{ O }_{ 3 }{ \rightarrow 4\div 3Al+O }_{ 2 }$
Here, the value of n = ${ 4 }$
Now, put the values in the equation 1, we get
$ { 960\times 10 }^{ 3 }{ J }mol^{ -1 }= { =\quad -4\times 96500\times E }^{ \circ }$
${ E }^{ \circ }{ =\quad -960000\div 4\times 96500 }$
${ E }^{ \circ }= { =\quad -960000\div 386000 }$
${ E }^{ \circ } = { -2.48V }$
So, difference = ${ 2.5V }$.
Hence, The potential difference needed for the electrolytic reduction of aluminium oxide ${ Al }_{ 2 }{ O }_{ 3 }$ at ${ 500 }^{ \circ }{ C }$ is at least ${ 2.5V }$.
The correct option is B.
> The metals present at the top of the reactivity series such as sodium and potassium can't be reduced using coke, therefore bypassing electric current through their molten salts they are reduced such a process to get metal from its metallic oxide is called Electrolytic Reduction.
> In the spontaneous process, the ${ \Delta G }$ ( free energy change ) must be a negative value.
Note: The possibility to make a mistake is that you have to convert Gibbs’ free energy in J/mol to kJ/mol. Also, the value of electrons transferred in this reaction is ${ 4 }$.
Recently Updated Pages
JEE Isolation, Preparation and Properties of Non-metals Important Concepts and Tips for Exam Preparation

Isoelectronic Definition in Chemistry: Meaning, Examples & Trends

Ionisation Energy and Ionisation Potential Explained

Iodoform Reactions - Important Concepts and Tips for JEE

Introduction to Dimensions: Understanding the Basics

Instantaneous Velocity Explained: Formula, Examples & Graphs

Trending doubts
JEE Main 2026: Exam Dates, Session 2 Updates, City Slip, Admit Card & Latest News

Hybridisation in Chemistry – Concept, Types & Applications

JEE Main 2026 Application Login: Direct Link, Registration, Form Fill, and Steps

Understanding the Electric Field of a Uniformly Charged Ring

Derivation of Equation of Trajectory Explained for Students

JEE Main Marking Scheme 2026- Paper-Wise Marks Distribution and Negative Marking Details

Other Pages
JEE Advanced Marks vs Ranks 2025: Understanding Category-wise Qualifying Marks and Previous Year Cut-offs

JEE Advanced 2026 - Exam Date (Released), Syllabus, Registration, Eligibility, Preparation, and More

CBSE Notes Class 11 Chemistry Chapter 9 - Hydrocarbons - 2025-26

CBSE Notes Class 11 Chemistry Chapter 5 - Thermodynamics - 2025-26

CBSE Notes Class 11 Chemistry Chapter 8 - Organic Chemistry Some Basic Principles And Techniques - 2025-26

JEE Advanced Weightage 2025 Chapter-Wise for Physics, Maths and Chemistry

