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
267.9k+ 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
Algebra Made Easy: Step-by-Step Guide for Students

JEE Isolation, Preparation and Properties of Non-metals Important Concepts and Tips for Exam Preparation

JEE Energetics Important Concepts and Tips for Exam Preparation

Chemical Properties of Hydrogen - Important Concepts for JEE Exam Preparation

JEE General Topics in Chemistry Important Concepts and Tips

JEE Amino Acids and Peptides Important Concepts and Tips for Exam Preparation

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

Understanding the Electric Field of a Uniformly Charged Ring

Derivation of Equation of Trajectory Explained for Students

Understanding Atomic Structure for Beginners

How to Convert a Galvanometer into an Ammeter or Voltmeter

Other Pages
JEE Advanced 2026 Notification Out with Exam Date, Registration (Extended), Syllabus and More

JEE Advanced Percentile vs Marks 2026: JEE Main Cutoff, AIR & IIT Admission Guide

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

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

