The Van't Hoff factor calculated from association data is always... than calculated from dissociation data
A. Less
B. More
C. Same
D. More or less
Answer
258.9k+ views
Hint: In the event of solute association, where the observed molecular weight of the solute is larger than the normal, the value of the factor \[i\] is less than unity (that is, \[i < 1\] ), whereas in the case of dissociation, where the observed molecular weight is greater than the normal molecular weight.
Complete step-by-step answer:A solute's impact on associated properties, such as osmotic pressure, relative vapour pressure reduction, boiling-point elevation, and freezing-point depression, is measured by the Van 't Hoff factor, \[i\] . The ratio of the observed or practical colligative quality to the theoretical colligative property is known as the Van't Hoff factor. The fraction of the solute that dissociates in the solution is known as the degree of dissociation. By taking into account both the theoretical and actual dissociation of the electrolyte in the solution, we may determine the relationship between the degree of dissociation and Van't Hoff factor, \[i\] .
The type of solute has no bearing on the properties of the solution; only its proportion or concentration does. The number of particles in a solution increases when polar or ionic solutes are dissolved in polar solvents because they become dissociated. As a result, the computed molar mass, turns out to be less than the theoretical molar mass.
In case of association, 2 molecules will combine to become one associated chemical entity which as higher molecular weight than individual molecules.
The Van't Hoff factor for association is more than 1 and for dissociation is less than 1.
Therefore, the Van't Hoff factor calculated from association data is always less than calculated from dissociation data
Option ‘A’ is correct
Note: Finding the true molar mass of a polar solute becomes challenging at large concentrations of the solute in a solution. As a result, the abnormal molar mass is determined, and the Van't Hoff factor \[i\] is used to determine the true molar mass from it. For dissociation, association, and the non-electrolyte solute, the Van't Hoff factor value is more than one, less than one, and equal to one respectively.
Complete step-by-step answer:A solute's impact on associated properties, such as osmotic pressure, relative vapour pressure reduction, boiling-point elevation, and freezing-point depression, is measured by the Van 't Hoff factor, \[i\] . The ratio of the observed or practical colligative quality to the theoretical colligative property is known as the Van't Hoff factor. The fraction of the solute that dissociates in the solution is known as the degree of dissociation. By taking into account both the theoretical and actual dissociation of the electrolyte in the solution, we may determine the relationship between the degree of dissociation and Van't Hoff factor, \[i\] .
The type of solute has no bearing on the properties of the solution; only its proportion or concentration does. The number of particles in a solution increases when polar or ionic solutes are dissolved in polar solvents because they become dissociated. As a result, the computed molar mass, turns out to be less than the theoretical molar mass.
In case of association, 2 molecules will combine to become one associated chemical entity which as higher molecular weight than individual molecules.
The Van't Hoff factor for association is more than 1 and for dissociation is less than 1.
Therefore, the Van't Hoff factor calculated from association data is always less than calculated from dissociation data
Option ‘A’ is correct
Note: Finding the true molar mass of a polar solute becomes challenging at large concentrations of the solute in a solution. As a result, the abnormal molar mass is determined, and the Van't Hoff factor \[i\] is used to determine the true molar mass from it. For dissociation, association, and the non-electrolyte solute, the Van't Hoff factor value is more than one, less than one, and equal to one respectively.
Recently Updated Pages
JEE Main Mock Test 2025-26: Principles Related To Practical

JEE Main 2025-26 Mock Test: Organic Compounds Containing Nitrogen

JEE Main Mock Test 2025-26: Purification & Characterisation of Organic Compounds

JEE Main 2025-26 Mock Test: Principles Related To Practical

JEE Main Mock Test 2025-26: Principles & Best Practices

Purification and Characterisation of Organic Compounds JEE Main 2025-26 Mock Test

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

JEE Main Participating Colleges 2026 - A Complete List of Top Colleges

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

Hybridisation in Chemistry – Concept, Types & Applications

Understanding the Electric Field of a Uniformly Charged Ring

Understanding the Different Types of Solutions in Chemistry

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

CBSE Class 12 Chemistry Question Paper 2026 PDF Download (All Sets) with Answer Key

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

NCERT Solutions For Class 12 Chemistry Chapter 2 Electrochemistry - 2025-26

NCERT Solutions For Class 12 Chemistry Chapter 1 Solutions - 2025-26

NCERT Solutions For Class 12 Chemistry Chapter 3 Chemical Kinetics - 2025-26

