Q.Calculate the osmotic pressure in pascals exerted by a solution prepared by dissolving 1.0 g of polymer of molar mass 185,000 in 450 mL of water at 37∘C.
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Osmotic Pressure and Molar Mass: From Intuition to Formula
Imagine you have a glass of pure water, and you carefully place a tea bag into it. After a while, the water turns brown. The tea molecules have moved from the bag into the water. That's simple diffusion. But now imagine a different setup: you have a U-shaped tube with a special membrane at the bottom that only lets water molecules pass through — not larger molecules like sugar. On one side you put pure water, on the other side you put a sugar solution. What happens?
Water will spontaneously move from the pure water side into the sugar solution side, pushing the liquid level higher on the sugar side. That rising column of liquid is a direct physical effect — it's osmotic pressure trying to equalise concentrations. The taller the column gets, the more hydrostatic pressure it exerts back. Eventually, that back-pressure exactly balances the "pull" of the sugar, and the system stops.
That balancing pressure — the pressure you would need to apply to the solution side to prevent the water from moving — is the osmotic pressure (Π).
The Intuition Behind Molar Mass from Osmotic Pressure
Here's the key insight: the osmotic pressure depends only on the number of solute particles in a given volume of solution, not on what those particles are. A big protein molecule and a tiny sugar molecule, if present in the same number per litre, produce the same osmotic pressure.
This is incredibly useful. If you dissolve an unknown substance (say, a polymer or a protein) in water and measure the osmotic pressure, you can work backwards to find how many moles of it are present. And if you know the mass you dissolved, you can calculate the molar mass:
Molar mass=number of molesmass of solute (g)
So osmotic pressure becomes a direct window into the molecular weight of substances that are too large or too fragile to vaporise (like proteins, polymers, or enzymes).
The Precise Statement
For dilute solutions, osmotic pressure follows a law that looks exactly like the ideal gas law:
ΠV=nRT
where:
- Π = osmotic pressure (in atm or Pa)
- V = volume of solution (in L or m³)
- n = number of moles of solute
- R = ideal gas constant (0.0821 L·atm·mol⁻¹·K⁻¹ or 8.314 J·mol⁻¹·K⁻¹)
- T = absolute temperature (in K)
This is the van't Hoff equation for osmotic pressure. It tells you that osmotic pressure is directly proportional to the molar concentration of the solute:
Π=VnRT=cRT
where c is the molar concentration (mol/L).
From Osmotic Pressure to Molar Mass
If you dissolve a known mass w (in grams) of an unknown substance in a volume V of solvent, and measure the osmotic pressure Π at temperature T, you can find the molar mass M as follows:
- From ΠV=nRT, we get n=RTΠV
- But n=Mw (mass divided by molar mass)
- Equating: Mw=RTΠV
- Rearranging:
M=ΠVwRT
This is the working formula. Every quantity on the right is measurable in the lab.
Why This Method is Special
Osmotic pressure measurements are extraordinarily sensitive. For a substance with a very large molar mass (say, 100,000 g/mol), the freezing point depression or boiling point elevation would be too tiny to measure accurately. But osmotic pressure can still give a measurable reading because it's a colligative property that depends only on particle count, and the effect is large even at low concentrations.
Osmotic pressure is the most sensitive colligative property for determining molar masses of macromolecules. It can detect concentrations as low as 10−4 M, which is 100–1000 times more sensitive than freezing point depression.
A Worked Example
Problem: 0.50 g of a protein is dissolved in enough water to make 100 mL of solution at 25°C. The osmotic pressure is measured as 0.012 atm. Find the molar mass of the protein.
Solution:
Given: …
Why this formula?
Great — let’s build a clear, concept-first understanding of Osmotic Pressure and its link to Molar Mass.
1. What is Osmotic Pressure?
Osmotic pressure (Π) is the minimum pressure that must be applied to a solution to prevent the net flow of solvent into it through a semipermeable membrane.
Think of it as the “push” needed to stop the solvent from diluting the solution.
2. The Key Formula
The central equation is:
Π=iCRT
Where:
- Π = osmotic pressure (atm or Pa)
- i = van’t Hoff factor (number of particles per formula unit)
- C = molar concentration (mol/L or mol/m³)
- R = universal gas constant
- T = absolute temperature (K)
For non-electrolytes (like glucose, urea), i=1, so:
Π=CRT
3. Why does this formula hold? — The Reasoning
Step 1: Analogy to Ideal Gas Law
The van’t Hoff equation for osmotic pressure is structurally identical to the ideal gas law:
PV=nRT⇒P=VnRT=CRT
Why? Because solute particles in a dilute solution behave like gas molecules — they are far apart, move randomly, and exert a “pressure” on the membrane.
- In a gas: particles hit the container walls → pressure.
- In a solution: solute particles cannot cross the membrane, but they collide with it → osmotic pressure.
So, the formula Π=CRT is not a coincidence — it’s a direct analogy.
Step 2: The van’t Hoff Factor i
For electrolytes (e.g., NaCl), one formula unit dissociates into multiple ions:
- NaCl → Na⁺ + Cl⁻ → i=2
- CaCl₂ → Ca²⁺ + 2Cl⁻ → i=3
Each ion acts as an independent particle, so the effective concentration increases by factor i:
Π=iCRT
Step 3: Linking to Molar Mass
We usually know mass of solute (w) and volume of solution (V). Molar concentration is:
C=Vn=Vw/M
where M = molar mass (g/mol).
Substitute into the osmotic pressure equation:
Π=i⋅MVw⋅RT
Rearrange to solve for molar mass:
M=ΠViwRT
This is the key formula used in experiments to find molar mass from osmotic pressure.
4. Why is this method special? …
The key idea is that osmotic pressure (Π) for a dilute solution follows van't Hoff's law: Π=iCRT, and for a non-electrolyte polymer, i=1.
Step 1: Find the molar concentration C.
Mass of polymer = 1.0 g, molar mass M=185,000 g/mol.
Moles of polymer = 185,0001.0=5.405×10−6 mol.
Volume of solution = 450 mL = 0.450 L.
C=0.4505.405×10−6=1.201×10−5 mol/L.
Step 2: Convert to SI units.
C in mol/m3: 1.201×10−5 mol/L = 1.201×10−2 mol/m3 (since 1 L = 10−3 m3).
Temperature T=37∘C = 310 K. …
Osmotic pressure depends only on the number of solute particles, not their identity. Using Π=iCRT (with i=1 for a non-electrolyte polymer), the pressure is about 31.0 Pa.
Why osmotic pressure works for molar mass
Osmotic pressure is a colligative property - it depends solely on the concentration of solute particles, not on their chemical nature. For a non-electrolyte like a polymer, each molecule contributes one particle, so i=1. This makes osmotic pressure ideal for finding the molar mass of large molecules: even a tiny mass of polymer gives a measurable pressure, whereas boiling point elevation or freezing point depression would be too small to detect.
The governing equation is:
Π=iCRT=VnRT=MVwRT
where Π is osmotic pressure (Pa), w is mass of solute (g), M is molar mass (g/mol), V is volume of solution (m3), R is the gas constant, and T is absolute temperature (K).
Step-by-step calculation
1. Convert temperature to Kelvin
T=37+273=310 K
2. Use SI gas constant
R=8.314 J mol−1K−1=8.314 Pa m3 mol−1K−1
3. Convert volume to cubic metres
V=450×10−6=4.50×10−4 m3 …
Method: Osmotic Pressure Formula (van't Hoff Equation)
This method uses the direct relationship between osmotic pressure and molar concentration for non-electrolyte solutions.
Steps
- Identify the formula The van't Hoff equation for osmotic pressure is:
Π=iCRT
For a non-electrolyte polymer, i=1, so:
Π=CRT
- Convert temperature to Kelvin
T=37∘C+273=310 K
- Calculate the molar concentration (C)
- Moles of polymer:
n=molar massmass=185,000 g/mol1.0 g=5.405×10−6 mol
- Volume in litres:
V=450 mL=0.450 L
- Molarity:
C=Vn=0.4505.405×10−6=1.201×10−5 mol/L
- Use the value of R in SI units For pressure in pascals (Pa), use:
R=8.314 J mol−1K−1=8.314 Pa m3mol−1K−1
Note: 1 L=10−3 m3, so C in mol/m3 is: …
Let’s first solve it correctly, then list the common mistakes and how to avoid each.
✓ Correct Solution (for reference)
Given:
- Mass of polymer, w=1.0 g
- Molar mass, M=185,000 g mol−1
- Volume of solution, V=450 mL=0.450 L
- Temperature, T=37∘C=37+273=310 K
- Gas constant, R=0.0821 L atm mol−1K−1 (for atm) or R=8.314 J mol−1K−1 (for Pa)
Step 1: Number of moles
n=Mw=185,0001.0=5.405×10−6 mol
Step 2: Molarity
C=V(L)n=0.4505.405×10−6=1.201×10−5 mol L−1
Step 3: Osmotic pressure (in Pa)
Use Π=CRT with R=8.314 J mol−1K−1 and C in mol m−3.
Convert molarity to mol m−3:
1 mol L−1=1000 mol m−3
So,
C=1.201×10−5×1000=1.201×10−2 mol m−3
Now,
Π=(1.201×10−2)×(8.314)×(310)
Π=1.201×10−2×2577.34≈30.95 Pa
Final answer: 30.95 Pa (approximately 31 Pa)
✗ Common Mistakes & How to Avoid Them
1. Forgetting to convert temperature to Kelvin
- Mistake: Using T=37∘C directly in Π=CRT.
- Why it’s wrong: The gas constant R has units per Kelvin — using Celsius gives a completely wrong (and meaningless) result.
- How to avoid: Always add 273 to Celsius: T(K)=T(∘C)+273. For 37°C, it’s 310 K.
2. Using wrong units for volume
- Mistake: Plugging V=450 mL directly into C=n/V without converting to litres.
- Why it’s wrong: Molarity is moles per litre, not per mL.
- How to avoid: Convert mL to L by dividing by 1000: 450 mL=0.450 L.
3. Confusing molar mass with molecular mass in g/mol
- Mistake: Treating 185,000 as the mass of one molecule (in amu) and then using it incorrectly.
- Why it’s wrong: Molar mass is already in g/mol — no further conversion needed.
- How to avoid: Remember: molar mass (g/mol) = molecular mass (amu) numerically. Just use it directly in n=w/M.
4. Using the wrong value of R for the required unit of pressure
- Mistake: Using R=0.0821 L atm mol−1K−1 and then reporting pressure in pascals without converting.
- Why it’s wrong: That R gives pressure in atm, not Pa.
- How to avoid:
- If answer needed in Pa, use R=8.314 J mol−1K−1 and ensure concentration is in mol m−3.
- If you use R=0.0821, convert atm to Pa: 1 atm=101325 Pa.
5. Forgetting to convert molarity to mol m−3 when using R=8.314
- Mistake: Plugging C in mol L−1 directly into Π=CRT with R=8.314. …
- COMEDK 2025Set 2025-A1 markMCQQ.A dilute solution of an ionic compound A3 B has an Osmotic pressure which is 6 times that of 0.02MMgCl2. What is the molar concentration of A3 B assuming that it undergoes complete dissociation in water? (A) 0.03 M (B) 0.26 M (C) 0.12 M (D) 0.09 M
›Reveal solutionSolution
The key idea is that osmotic pressure depends on the total number of particles in solution (van’t Hoff factor). For complete dissociation, A3B gives 4 ions, and MgCl2 gives 3 ions. Setting ΠA3B=6×ΠMgCl2 and solving gives the molar concentration of A3B as 0.09 M, which corresponds to option (D).
Concept & Intuition
Osmotic pressure (Π) is a colligative property — it depends only on the number of solute particles, not their identity. For ionic compounds that dissociate completely, the effective particle concentration is the molar concentration multiplied by the van’t Hoff factor i (the number of ions per formula unit).
Here, A3B dissociates into 3 A⁺ ions and 1 B³⁻ ion, so i=4. MgCl2 dissociates into 1 Mg²⁺ and 2 Cl⁻, so i=3.
The problem states: ΠA3B=6×ΠMgCl2. Since Π=iCRT (with R and T constant), we can cancel RT and solve for the unknown concentration CA3B.
Step-by-step solution
-
Write the osmotic pressure formula
For any solution, Π=iCRT, where C is the molar concentration, i is the van’t Hoff factor, R is the gas constant, and T is the absolute temperature. Since both solutions are at the same T, R and T cancel when we compare them.
-
Determine van’t Hoff factors
- MgCl2→Mg2++2Cl− → i=1+2=3
- A3B→3A++B3− → i=3+1=4
-
Set up the given relationship
ΠA3B=6×ΠMgCl2
Substitute Π=iCRT:
4×CA3B×RT=6×(3×0.02×RT)
- Cancel RT (same for both sides) …
-
- COMEDK 2025Set 2025-E1 markMCQQ.An aqueous solution of volume V ml contains a non-volatile solute of unknown mass WB g and molar mass MB g/mol. If the Osmotic pressure of the solution is 1.013 bar, which one of the following is the mathematical expression to be used to calculate WB ? (A) WB=760∗RT∗1000πMBV (B) WB=76RTπMBV1000 (C) WB=RTπMBV (D) WB=1000RTπMBV
›Reveal solutionSolution
The key is to use the van’t Hoff equation for osmotic pressure, π=cRT, where c is molarity in mol/L, and then carefully convert units so that volume in mL and mass in grams yield the correct expression. The correct option is (D).
The problem gives osmotic pressure in bar, volume in mL, mass in grams, and molar mass in g/mol. The van’t Hoff law says π=cRT, where c is concentration in mol/L. Since c=Vlitersn and n=MBWB, we just need to handle the volume conversion from mL to L. The trick is that many options include extra factors like 760 or 76, which come from converting pressure units (e.g., atm to mm Hg), but here pressure is already in bar — and if we use R in appropriate units, no such factor is needed. Let’s derive step by step.
- Start with the van’t Hoff equation Osmotic pressure π (in bar) is related to molar concentration c (in mol/L) by
π=cRT
where R is the gas constant in L·bar/(mol·K) and T is temperature in K.
- Express concentration in terms of given quantities Molarity c=volume in litersmoles of solute=V/1000WB/MB because V mL = V/1000 L. So
c=MBWB⋅V1000
- Substitute into the osmotic pressure equation
π=(MBWB⋅V1000)RT
- Solve for WB Multiply both sides by MBV and divide by 1000RT:
WB=1000RTπMBV
- Check the options …
- KCET 2024Set B-21 markMCQQ.The number of atoms in 4.5g of a face-centred cubic crystal with edge length 300pm is : (Given density =10g cm−3 and NA=6.022×1023). (A) 6.6×1020 (B) 6.6×1023 (C) 6.6×1019 (D) 6.6×1022
›Reveal solutionSolution
Get the sample volume from mass/density, divide by the unit-cell volume a3 to count unit cells, then multiply by Z=4 atoms per FCC cell — giving 6.6×1022 atoms.
Step 1 — Volume of the sample.
Density relates mass to volume:
Vsample=ρm=10 g cm−34.5 g=0.45 cm3
Step 2 — Volume of one FCC unit cell.
Convert the edge length to centimetres (to match the density's units):
a=300 pm=300×10−12 m=300×10−10 cm=3×10−8 cm
a3=(3×10−8)3=27×10−24 cm3=2.7×10−23 cm3
Step 3 — Number of unit cells in the sample.
ncells=a3Vsample=2.7×10−230.45=1.667×1022 unit cells
Step 4 — Atoms per FCC unit cell (Z).
In a face-centred cubic cell:
- 8 corner atoms, each shared by 8 cells ⇒8×81=1 atom;
- 6 face-centred atoms, each shared by 2 cells ⇒6×21=3 atoms.
Z=1+3=4
Step 5 — Total atoms. …
- COMEDK 2024Set 2024-E1 markMCQQ.
[!FORMULA] 200ml of an aqueous solution contains 3.6 g of Glucose and 1.2 g of Urea maintained at a temperature equal to 27∘C. What is the Osmotic pressure of the solution in atmosphere units? R=0.082 L atm K−1 mol−1 : Molecular Formula: Glucose is C6H12O6 and of Urea is NH2CONH2
(A) 6.24 (B) 1.56 (C) 9.84 (D) 4.92›Reveal solutionSolution
Total moles of solute =0.04, giving π=(n/V)RT=0.2×0.082×300=4.92 atm.
Moles of glucose =1803.6=0.02 mol.
Moles of urea =601.2=0.02 mol.
Both are non-electrolytes, so total solute particles n=0.02+0.02=0.04 mol.
Volume V=200 mL=0.2 L, T=27∘C=300 K. …
- KCET 2022Set B-31 markMCQQ.Which of the following colligative properties can provide molar mass of proteins, polymers, and colloids with greater precision? (A) Depression in freezing point (B) Osmotic pressure (C) Relative lowering of vapour pressure (D) Elevation in boiling point
›Reveal solutionSolution
Osmotic pressure is the only colligative property large enough to measure accurately for very dilute solutions of high-molar-mass solutes, so it is the method of choice for proteins, polymers and colloids.
Step 1 — Why the other three fail for macromolecules.
A macromolecule has a huge molar mass (M∼104–106 g/mol), so even a few grams dissolved give a tiny number of moles ⇒ a very small molality/mole fraction. Now look at the magnitudes each property produces:
ΔTf=Kfm,ΔTb=Kbm,p0p0−p=x2
With m∼10−4 mol/kg and Kf,Kb of order 1 K kg mol−1, we get ΔT∼10−4∘C — far below what an ordinary thermometer can resolve. Relative lowering of vapour pressure is equally negligible. Any measurement error is then enormous relative to the signal, so the computed M is unreliable.
Step 2 — Why osmotic pressure works.
π=CRT=VnRT=MVwRT
The multiplier here is RT≈0.0821×300≈25 L atm mol−1 — orders of magnitude larger in effect than Kf or Kb. A concentration of just 10−4 mol/L still gives …
- KCET 2022Set B-31 markMCQQ.If 3 g of glucose (molar mass =180g) is dissolved in 60 g of water at 15∘C, the osmotic pressure of the solution will be (A) 6.57 atm (B) 5.57 atm (C) 0.34 atm (D) 0.65 atm
›Reveal solutionSolution
Apply the van 't Hoff equation π=CRT=Mw⋅VRT, converting 60 g of water to 0.060 L and 15∘C to 288 K.
Step 1 — The governing law.
Osmotic pressure of a dilute solution (van 't Hoff):
π=CRT=VnRT=MVwRT
This is the colligative property that measures the pressure needed to stop solvent flowing into the solution through a semipermeable membrane. Glucose is a non-electrolyte (i=1), so no van 't Hoff factor correction is needed.
Step 2 — Compute the moles of solute.
n=Mw=180 g mol−13 g=0.01667 mol
Step 3 — Get the volume in litres.
The solution is dilute, so its volume is essentially the volume of the water. Using density of water =1 g/mL:
V=60 g×1 g1 mL=60 mL=0.060 L
Step 4 — Convert the temperature to kelvin.
T=15+273=288 K
(Never use ∘C in a gas-law-type equation — the T must be absolute.) …
- KCET 2020Set A-11 markMCQQ.Which of the following pair of solutions is isotonic ? (A) 0.01 M BaCl2 and 0.001 M CaCl2 (B) 0.01 M BaCl2 and 0.015 M NaCl (C) 0.001 M Al2(SO4)3 and 0.01 M BaCl2 (D) 0.001 M CaCl2 and 0.001 M Al2(SO4)3
›Reveal solutionSolution
Isotonic solutions have the same osmotic pressure, which depends on the total particle concentration after dissociation (van’t Hoff factor i). We compute i×C for each solution and compare. The correct pair is (B).
Concept & Intuition
Osmotic pressure Π is given by Π=iCRT, where C is the molar concentration, R is the gas constant, T is the temperature, and i is the van’t Hoff factor — the number of particles each formula unit produces in solution. For strong electrolytes (which all these salts are), i equals the number of ions per formula unit.
Two solutions are isotonic when their osmotic pressures are equal at the same temperature. Since R and T are constant, this reduces to comparing the product iC for each solution. The pair with matching iC values is the answer.
Watch outA common mistake is to compare only the molar concentrations C without accounting for dissociation. For example, 0.01 M BaCl2 and 0.01 M NaCl are not isotonic — BaCl2 gives 3 ions per formula, NaCl gives only 2.
Step-by-step solution
-
Determine the van’t Hoff factor i for each salt
- BaCl2→Ba2++2Cl− → i=3
- CaCl2→Ca2++2Cl− → i=3
- NaCl→Na++Cl− → i=2
- Al2(SO4)3→2Al3++3SO42− → i=5
-
Compute the effective particle concentration iC for each solution in the options
Option Solution C (M) i iC (M) (A) BaCl2 0.01 3 0.03 (A) CaCl2 0.001 3 0.003 (B) BaCl2 0.01 3 0.03
-
- KCET 2018Set A-11 markMCQQ.Isotonic solutions are solutions having the same (A) Surface tension (B) Vapour pressure (C) Osmotic pressure (D) Viscosity
›Reveal solutionSolution
'Isotonic' is defined by equality of osmotic pressure — this is a definition question about a colligative property.
Step 1 — The definition.
Osmotic pressure π is the pressure that must be applied to a solution to just stop the inward flow of solvent through a semipermeable membrane. Two solutions are said to be isotonic when
π1=π2at the same temperature
Placed on either side of a semipermeable membrane, isotonic solutions show no net osmosis — solvent crosses both ways at equal rates.
Step 2 — What that implies about concentration.
From the van't Hoff equation for dilute solutions,
π=CRT(or π=iCRT for electrolytes)
so at the same T, isotonic solutions have the same molar concentration of solute particles — e.g. 0.91% NaCl (normal saline) is isotonic with human blood cells, which is why it can be safely infused.
Step 3 — Rule out the others. …
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