Question:

The following solutions were prepared by dissolving $10 g$ of glucose $\left( C _{6} H _{12} O _{6}\right)$ in $250 \,ml$ of water $\left( P _{1}\right)$ $10 \,g$ of urea $\left( CH _{4} N _{2} O \right)$ in $250 \,ml$ of water $\left( P _{2}\right)$ and $10 g$ of sucrose $\left( C _{12} H _{22} O _{11}\right)$ in $250\, ml$ of water $\left( P _{3}\right)$. The right option for the decreasing order of osmotic pressure of these solutions is:

Updated On: Nov 13, 2025
  • $P _{2}> P _{1}> P _{3}$
  • $P _{1}> P _{2}> P _{3}$
  • $P _{2}> P _{3}> P _{1}$
  • $P _{3}> P _{1}> P _{2}$
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The Correct Option is A

Approach Solution - 1

To determine the decreasing order of osmotic pressure for the given solutions, we must understand the concept of osmotic pressure. Osmotic pressure is a colligative property, meaning it depends on the number of solute particles in a solution and not on the nature of the solute itself. The formula for osmotic pressure \((\pi)\) is given by: 

\(\pi = iCRT\)

  • \(i\) is the van't Hoff factor (number of particles the solute dissociates into)
  • \(C\) is the molar concentration of the solution
  • \(R\) is the universal gas constant
  • \(T\) is the temperature in Kelvin

In the given problem, the solute and solvent amounts are the same for each solution, so the concentration \((C)\) can be calculated using:

Molar mass of glucose \((C_{6}H_{12}O_{6})\) = 180 g/mol

Molar mass of urea \((CH_{4}N_{2}O)\) = 60 g/mol

Molar mass of sucrose \((C_{12}H_{22}O_{11})\) = 342 g/mol

For glucose \((P_1)\)\(10\, g\) of glucose is dissolved. The number of moles of glucose is:

\(\text{Moles of glucose} = \frac{10}{180} = 0.0556 \text{ mol}\)

For urea \((P_2)\)\(10\, g\) of urea is dissolved. The number of moles of urea is:

\(\text{Moles of urea} = \frac{10}{60} = 0.1667 \text{ mol}\)

For sucrose \((P_3)\)\(10\, g\) of sucrose is dissolved. The number of moles of sucrose is:

\(\text{Moles of sucrose} = \frac{10}{342} = 0.0292 \text{ mol}\)

Since all the solutes are non-ionic compounds without dissociation in water, the van’t Hoff factor \((i)\) for all is 1. Thus, the osmotic pressure is directly proportional to the number of moles of solute present in the solution.

Comparing the moles of the solute, we have:

  • Urea has the greatest number of moles (0.1667 mol), so \(P_2\) will have the highest osmotic pressure.
  • Glucose has the next greatest number of moles (0.0556 mol), so \(P_1\) will have an intermediate osmotic pressure.
  • Sucrose has the least number of moles (0.0292 mol), so \(P_3\) will have the lowest osmotic pressure.

Thus, the decreasing order of osmotic pressure is:

\(P_2 > P_1 > P_3\)

Therefore, the correct answer is:

\(P_2 > P_1 > P_3\)

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Approach Solution -2

$\pi=\frac{W}{M} S T$ $\pi \propto \frac{1}{\text { Mol.wt }}$ Glucose $(180)$, Urea $(60)$, Sucrose $(342)$ $\pi_{\text {urea }}>\pi_{\text {glucose }}>\pi_{\text {sucrose }}$ $P_{2}>P_{1}>P_{3}$

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Concepts Used:

Colligative Properties

Colligative Property of any substance is entirely dependent on the ratio of the number of solute particles to the total number of solvent particles but does not depend on the nature of particles. There are four colligative properties: vapor pressure lowering, boiling point elevation, freezing point depression, and osmotic pressure.

Examples of Colligative Properties

We can notice the colligative properties of arrangements by going through the accompanying examples:

  • On the off chance that we add a spot of salt to a glass full of water, its freezing temperature is brought down impressively than its normal temperature. On the other hand, the boiling temperature is likewise increased and the arrangement will have a lower vapor pressure. There are also changes observed in its osmotic pressure.
  • In the same way, if we add alcohol to water, the solution’s freezing point goes down below the normal temperature that is usually observed for either pure alcohol or water.

Types of Colligative Properties

  1. Freezing point depression: ΔTf =1000 x kf x m2 /(M2 x m1)
  2. Boiling point elevation: ΔTb = kb m
  3. Osmotic pressure: π = (n2/V) RT
  4. Relative lowering of vapor pressure: (Po - Ps)/Po