Q.18 g of glucose, C6H12O6, is dissolved in 1 kg of water in a saucepan. At what temperature will water boil at 1.013 bar? Kb for water is 0.52 K kg mol−1.
Concept understanding — Boiling Point Elevation
Boiling Point Elevation — From Intuition to Precision
Imagine you're cooking pasta. You add salt to the water, and the water takes longer to boil. That's not your imagination — it's a real physical effect. The salt has raised the boiling point of the water. Pure water boils at 100°C at sea level, but salt water needs a slightly higher temperature to boil. That's boiling point elevation in action.
Why does this happen?
To understand why, you need to think about what boiling actually is. Boiling occurs when the vapour pressure of the liquid equals the surrounding atmospheric pressure. Vapour pressure is the pressure exerted by molecules escaping from the liquid surface into the gas phase.
When you dissolve a non-volatile solute (like salt, which doesn't evaporate) in a solvent (like water), something interesting happens at the surface. Some of the surface molecules are now solute particles — they don't escape into the vapour. This means fewer solvent molecules can leave the liquid per second. The result? The vapour pressure of the solution is lower than that of the pure solvent at the same temperature.
Now, to make this reduced vapour pressure equal to the atmospheric pressure (so the liquid can boil), you need to raise the temperature. That extra heat gives the remaining solvent molecules enough energy to overcome the solute's interference and produce the required vapour pressure.
The solute itself doesn't boil away — it stays behind. That's why we call it a non-volatile solute. If the solute were volatile (like alcohol), the story changes.
The precise statement
Boiling point elevation is the increase in the boiling point of a solvent when a non-volatile solute is dissolved in it. The boiling point of the solution is always higher than that of the pure solvent.
The elevation ΔTb is given by:
ΔTb=Tb(solution)−Tb(pure solvent)
And it depends only on the number of solute particles, not on their chemical identity (for dilute solutions). This is a colligative property — a property that depends on the concentration of particles, not their nature.
ΔTb=Kb⋅m
Where:
- ΔTb = boiling point elevation (in °C or K)
- Kb = ebullioscopic constant of the solvent (a fixed value for each solvent)
- m = molality of the solution (moles of solute per kg of solvent)
What is Kb?
The ebullioscopic constant Kb is a property of the pure solvent. It tells you how much the boiling point rises per unit molal concentration. For water, Kb=0.512°C kg mol−1. So a 1 molal aqueous solution (1 mole of solute per kg of water) boils at 100.512°C.
For quick calculations: ΔTb∝m. Double the molality, double the elevation. But this works only for dilute solutions — at high concentrations, interactions between solute particles break the linearity.
What about electrolytes?
If the solute dissociates into ions (like NaCl → Na⁺ + Cl⁻), the number of particles increases. One mole of NaCl gives two moles of particles in solution. So the effective concentration is higher. We account for this using the van't Hoff factor i:
ΔTb=i⋅Kb⋅m
For NaCl, i≈2 (in dilute solutions). For sugar (which doesn't dissociate), i=1.
Never forget the van't Hoff factor for ionic solutes. A common mistake is to treat NaCl as one particle — it's two. That doubles the elevation.
A quick example
You dissolve 58.5 g of NaCl (molar mass = 58.5 g/mol) in 500 g of water. What is the boiling point of the solution? (Kb for water = 0.512 °C kg mol⁻¹)
- Moles of NaCl = 58.5/58.5=1.0 mol
- Molality m=1.0 mol/0.500 kg=2.0 mol/kg
- For NaCl, i=2, so effective molality = 2×2.0=4.0 mol/kg
- ΔTb=0.512×4.0=2.048°C
- Boiling point = 100+2.048=102.048°C
The boiling point elevation depends on the number of particles in solution, not their mass or identity. That's why 1 mole of NaCl raises the boiling point twice as much as 1 mole of sugar.
Why does this matter in exams?
Boiling point elevation is a standard topic in physical chemistry (Class 12 CBSE, JEE, NEET). You'll be asked to:
- Calculate ΔTb given mass of solute, solvent, and Kb
- Compare boiling points of different solutions
- Determine molar mass of an unknown solute using ΔTb
- Apply the van't Hoff factor for electrolytes
The key is to remember: more particles → higher boiling point. Everything else follows from that single idea.
Searches like "boiling point elevation formula chemistry" and "colligative properties class 12 numericals" point directly to the Solutions chapter of the NCERT/CBSE Class 12 Chemistry curriculum. The van't Hoff factor correction for electrolytes in particular is a very common JEE Main and NEET question.
Why this formula?
Boiling Point Elevation: Why the Formula Holds
Let's build this from first principles — understanding the why before the what.
What Happens at the Boiling Point?
At the boiling point, a liquid's vapor pressure equals the external atmospheric pressure. For a pure solvent, this happens at a fixed temperature (e.g., 100°C for water at 1 atm).
When you add a non-volatile solute (like salt or sugar), the solute particles occupy space at the liquid surface, reducing the number of solvent molecules that can escape into vapor. This lowers the vapor pressure of the solution compared to the pure solvent.
The Key Consequence
Since vapor pressure is now lower, the solution must be heated to a higher temperature to make its vapor pressure reach atmospheric pressure again. That's the boiling point elevation.
The Formula and Its Derivation
The boiling point elevation ΔTb is given by:
ΔTb=Kb⋅m
where:
- ΔTb=Tb(solution)−Tb(pure solvent)
- Kb = ebullioscopic constant (depends only on the solvent)
- m = molality of the solution (moles of solute per kg of solvent)
Why Molality and Not Molarity?
Molality is temperature-independent — it doesn't change when the solution is heated. Molarity (moles per liter) changes because volume expands with temperature. Since we're measuring a temperature change, we need a concentration unit that stays fixed.
The Reasoning Behind Kb
The constant Kb comes from thermodynamics. For a dilute solution, the vapor pressure lowering follows Raoult's Law:
Psolution=xsolvent⋅Psolvent0
where xsolvent is the mole fraction of solvent and Psolvent0 is the pure solvent's vapor pressure.
Using the Clausius-Clapeyron equation (which relates vapor pressure to temperature) and Raoult's Law, one can derive:
Kb=1000⋅ΔHvapRTb2
where:
- R = gas constant (8.314 J/mol·K)
- Tb = boiling point of pure solvent (in Kelvin)
- ΔHvap = molar enthalpy of vaporization (J/mol)
- The factor 1000 converts grams to kg (since molality uses kg of solvent)
What This Tells Us
- Kb is a property of the solvent alone — it doesn't depend on the solute.
- Solvents with higher boiling points or lower heats of vaporization have larger Kb values (greater elevation per molal concentration).
Why the Formula is Linear (for Dilute Solutions)
For dilute solutions, the mole fraction of solvent is approximately:
xsolvent≈1−nsolventnsolute
The vapor pressure lowering is proportional to the solute mole fraction. Since molality m∝nsolventnsolute for dilute solutions, the boiling point elevation becomes directly proportional to m.
This linearity breaks down at high concentrations — then we need more complex models.
Exam-Relevant Summary
| Concept | Key Point |
|---|---|
| Cause | Non-volatile solute lowers vapor pressure |
| Effect | Higher temperature needed to boil |
| Formula | ΔTb=Kb⋅m |
| Kb depends on | Solvent only (Tb, ΔHvap) |
| Concentration unit | Molality (temperature-independent) |
| Valid for | Dilute solutions (linear approximation) |
Remember: The formula is not magic — it's a direct consequence of vapor pressure lowering combined with the thermodynamics of phase equilibrium.
Concept: Boiling Point Elevation — the increase in boiling point when a non-volatile solute is added to a solvent.
Step 1: Find moles of glucose
Molar mass of C6H12O6=180 g mol−1
Moles =18018=0.1 mol
Step 2: Find molality
Mass of solvent =1 kg
Molality m=10.1=0.1 mol kg−1
Step 3: Apply boiling point elevation formula
ΔTb=Kb⋅m=0.52×0.1=0.052 K
Step 4: New boiling point
At 1.013 bar, pure water boils at 100∘C.
Boiling point =100+0.052=100.052∘C
The water will boil at 100.052∘C.
Molality =0.1 mol kg−1, so ΔTb=Kbm=0.52×0.1=0.052 K, giving a boiling point of 373.15+0.052=373.20 K (≈100.05∘C).
Molality. Molar mass of glucose C6H12O6=180 g mol−1:
n=18018=0.1 mol,m=1 kg0.1 mol=0.1 mol kg−1.
Elevation in boiling point.
ΔTb=Kbm=0.52 K kg mol−1×0.1 mol kg−1=0.052 K.
Boiling point. Pure water boils at 373.15 K at 1.013 bar, so
Tb=373.15+0.052=373.202 K≈100.05∘C.
The solution boils at about 373.20 K (≈100.05∘C).
Method: Boiling Point Elevation Formula
This is a direct application of the boiling point elevation formula for non-volatile solutes.
Concept (Why this works)
When a non-volatile solute like glucose is dissolved in a solvent (water), the vapour pressure of the solvent decreases. To make the solution boil (i.e., reach atmospheric pressure), we need to raise the temperature above the normal boiling point. The increase is called boiling point elevation, ΔTb.
Formula
ΔTb=Kb×m
Where:
- ΔTb = elevation in boiling point (in K or °C)
- Kb = ebullioscopic constant of solvent (given: 0.52 K kg mol⁻¹)
- m = molality of solution (mol solute per kg solvent)
Steps
Step 1: Find moles of glucose
- Molar mass of glucose (C6H12O6) = 6(12)+12(1)+6(16)=180 g/mol
- Moles = 180 g/mol18 g=0.1 mol
Step 2: Find molality
- Mass of solvent (water) = 1 kg
- Molality, m=1 kg0.1 mol=0.1 mol/kg
Step 3: Calculate ΔTb
ΔTb=0.52×0.1=0.052 K
Step 4: Find boiling point of solution
- Normal boiling point of water at 1.013 bar = 100 °C (or 373.15 K)
- Boiling point of solution = 100+0.052=100.052∘C
Final Answer
The water will boil at 100.052 °C (or 373.202 K).
Here are the common mistakes students make with boiling point elevation problems — and how to avoid each one.
1. Forgetting that boiling point elevation is not the final boiling point
Mistake:
Students calculate ΔTb and stop there, writing the answer as 0.052∘C.
Why it’s wrong:
The question asks: At what temperature will water boil?
You must add ΔTb to the normal boiling point of water (100∘C at 1.013 bar).
How to avoid:
Always write the final step explicitly:
Tb=Tb∘+ΔTb
Here:
Tb=100+0.052=100.052∘C
Key result: 100.052∘C
2. Using mass of solute instead of moles in the molality formula
Mistake:
Plugging 18 g directly into ΔTb=Kb⋅m without converting to moles.
Why it’s wrong:
Molality m is moles of solute per kg of solvent, not grams per kg.
How to avoid:
Always compute moles first:
Moles of glucose=18018=0.1 mol
Then:
m=10.1=0.1 mol kg−1
3. Using the wrong molar mass for glucose
Mistake:
Using C6H12O6 molar mass as 160, 200, or forgetting to add oxygen.
Why it’s wrong:
Glucose = 6(12)+12(1)+6(16)=72+12+96=180 g mol−1.
How to avoid:
Write out the atomic masses clearly before calculating:
- Carbon: 6×12=72
- Hydrogen: 12×1=12
- Oxygen: 6×16=96
- Total: 180 g mol−1
4. Confusing molality with molarity
Mistake:
Using volume of solution (which isn’t given) instead of mass of solvent.
Why it’s wrong:
Boiling point elevation uses molality (m), not molarity (M).
Here, solvent mass is given as 1 kg — that’s perfect for molality.
How to avoid:
Check the units: if the problem gives kg of solvent, use molality.
If it gives volume of solution, you’d need density to convert — but that’s rare for this concept.
5. Forgetting that Kb units are K kg mol−1 — not just K
Mistake:
Plugging numbers without checking unit cancellation.
Why it’s wrong:
You need ΔTb in K (or ∘C, same magnitude).
Kb times molality gives:
0.52×0.1=0.052 K
How to avoid:
Write the units alongside each step:
ΔTb=(0.52K kg mol−1)×(0.1mol kg−1)=0.052K
6. Assuming glucose dissociates (like salt)
Mistake:
Using i=2 or another van’t Hoff factor.
Why it’s wrong:
Glucose is a non-electrolyte — it does not dissociate in water.
i=1 always for covalent molecular solutes like sugar.
How to avoid:
For molecular solutes (glucose, urea, sucrose), always use i=1.
Only use i>1 for ionic compounds (NaCl, CaCl2, etc.).
Quick checklist to avoid all mistakes
| Step | What to do |
|---|---|
| 1 | Find molar mass of solute |
| 2 | Convert mass to moles |
| 3 | Divide moles by kg of solvent → molality |
| 4 | Multiply by Kb → ΔTb |
| 5 | Add ΔTb to 100∘C |
| 6 | Write final answer with units |
Final answer:
100.052∘C
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