Q.Boiling point of water at 750 mm Hg is 99.63∘C. How much sucrose is to be added to 500 g of water such that it boils at 100∘C.
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.
This problem involves Boiling Point Elevation, a colligative property where the boiling point of a solvent increases upon the addition of a non-volatile solute.
-
First, calculate the elevation in boiling point (ΔTb):
ΔTb=Tb−Tb0=100∘C−99.63∘C=0.37∘C.
-
Next, use the boiling point elevation formula to find the molality (m) of the sucrose solution. The molal elevation constant (Kb) for water is 0.52 K kg mol−1 (or 0.52∘C kg mol−1).
ΔTb=Kb⋅m
0.37∘C=0.52∘C kg mol−1⋅m
m=0.520.37≈0.7115 mol kg−1
-
Now, calculate the moles of sucrose needed. The mass of water (solvent) is 500 g=0.5 kg.
Moles of sucrose = m×mass of water (kg)
Moles of sucrose = 0.7115 mol kg−1×0.5 kg=0.35575 mol
-
Finally, convert moles of sucrose to mass using its molar mass (C12H22O11), which is 342 g mol−1.
Mass of sucrose = Moles of sucrose × Molar mass of sucrose
Mass of sucrose = 0.35575 mol×342 g mol−1≈121.66 g
Approximately 121.66 g of sucrose must be added.
Boiling-point elevation (ΔTb=Kbm) is used to find the molality needed to raise water's boiling point from 99.63°C to 100°C, then converted to mass of sucrose. Approximately 121.7 g of sucrose must be added to 500 g of water.
Boiling-point elevation is a colligative property — it depends only on the number of solute particles dissolved in a fixed mass of solvent, not on their identity. For a non-volatile, non-electrolyte solute such as sucrose, the relationship is
ΔTb=Kbm
where ΔTb is the elevation in boiling point, Kb is the molal elevation (ebullioscopic) constant of the solvent, and m is the molality of the solution.
Step 1: Find the required boiling-point elevation
The water must boil at 100°C instead of its actual boiling point of 99.63°C at 750 mm Hg:
ΔTb=100°C−99.63°C=0.37 K
Step 2: Find the required molality
Using Kb=0.52 K kg mol−1 (as given for water):
m=KbΔTb=0.520.37=0.7115 mol kg−1
Step 3: Find the moles of sucrose needed
Molality is defined per kilogram of solvent. Here the solvent is 500 g = 0.500 kg of water:
nsucrose=m×wwater(kg)=0.7115×0.500=0.3558 mol
Step 4: Convert moles to mass
The molar mass of sucrose (C12H22O11) is 342 g mol−1:
wsucrose=nsucrose×Msucrose=0.3558×342=121.7 g
So dissolving about 121.7 g of sucrose in 500 g of water raises its boiling point by 0.37 K, bringing it exactly to 100°C at 750 mm Hg.
Mass of sucrose required ≈121.7 g (added to 500 g of water, using Kb=0.52 K kg mol−1 and Msucrose=342 g mol−1).
Method: Boiling Point Elevation Formula
This is a colligative property problem — the boiling point rises because solute particles (sucrose) lower the vapour pressure of the solvent (water).
Step 1 — Identify the given data
- Normal boiling point of water (at 750 mm Hg) = 99.63∘C
- Desired boiling point = 100∘C
- Mass of solvent (water) = 500 g
- Solute = sucrose (C12H22O11), molar mass = 342 g/mol
- Kb for water = 0.52 K kg mol−1 (standard value, must be known)
Step 2 — Calculate the elevation in boiling point
ΔTb=Tsolution−Tsolvent
ΔTb=100−99.63=0.37∘C
Step 3 — Apply the boiling point elevation formula
ΔTb=Kb⋅m
where m = molality of the solution (mol solute per kg solvent).
0.37=0.52×m
m=0.520.37≈0.7115 mol/kg
Step 4 — Find moles of sucrose needed
Molality m = mass of solvent in kgmoles of solute
Mass of water = 500 g=0.5 kg
0.7115=0.5moles of sucrose
moles of sucrose=0.7115×0.5≈0.3558 mol
Step 5 — Convert moles to mass
Mass=moles×molar mass
Mass=0.3558×342≈121.7 g
Final Answer:
121.7 g
Key concept check: Sucrose is non-volatile and does not dissociate — so i=1. If the solute were ionic (like NaCl), you would multiply by van’t Hoff factor i.
🧠 The Core Concept First
Boiling point elevation is a colligative property — it depends only on the number of solute particles, not their identity.
The formula is:
ΔTb=Kb⋅m
Where:
- ΔTb = elevation in boiling point (Tb−Tb0)
- Kb = ebullioscopic constant of the solvent (for water, Kb=0.52K kg mol−1)
- m = molality of the solution (moles of solute per kg of solvent)
🔍 Step-by-Step Solution (for reference)
Given:
- Initial boiling point of water = 99.63∘C at 750 mm Hg
- Final boiling point = 100∘C
- Mass of water = 500g=0.5kg
- Solute = sucrose (C12H22O11, molar mass = 342g/mol)
Step 1: Find ΔTb
ΔTb=100−99.63=0.37∘C
Step 2: Use ΔTb=Kb⋅m
0.37=0.52⋅m⇒m=0.520.37≈0.7115mol/kg
Step 3: Find moles of sucrose
moles=m×mass of solvent (kg)=0.7115×0.5≈0.3558mol
Step 4: Find mass of sucrose
mass=0.3558×342≈121.7g
✓ Final answer: Approximately 121.7 g of sucrose.
✗ Common Mistakes & How to Avoid Them
1. Using the wrong Kb value
- Mistake: Using Kb=0.512 or 0.52 without checking units or if it's for water.
- How to avoid: Memorise: Kb for water = 0.52 K kg mol⁻¹. Always confirm in the problem if given. If not, use the standard value.
2. Confusing molality with molarity
- Mistake: Using volume of solution instead of mass of solvent.
- How to avoid: Remember: molality = moles of solute / kg of solvent. Here, solvent is water — use its mass in kg, not volume.
3. Forgetting to convert grams to kg
- Mistake: Using 500 g directly as 500 kg in the molality formula.
- How to avoid: Always convert: 500g=0.5kg. Write it explicitly.
4. Using the wrong molar mass of sucrose
- Mistake: Taking 342 as 342 g (correct) but then using it in molality without converting.
- How to avoid: Double-check: C12H22O11 = 12(12)+22(1)+11(16)=144+22+176=342g/mol. Write it down.
5. Rounding off too early
- Mistake: Rounding 0.520.37 to 0.71 instead of 0.7115, then multiplying by 0.5 to get 0.355 instead of 0.3558.
- How to avoid: Keep at least 4 decimal places during intermediate steps. Round only at the final answer.
6. Assuming ΔTb is the final temperature
- Mistake: Writing ΔTb=100∘C.
- How to avoid: ΔTb is the change, not the final temperature. Always subtract: ΔTb=Tb−Tb0.
7. Ignoring the given pressure (750 mm Hg)
- Mistake: Thinking the pressure is irrelevant and using 100∘C as the normal boiling point.
- How to avoid: The problem gives the boiling point at 750 mm Hg as 99.63∘C. That is your Tb0. The normal boiling point (100∘C at 760 mm Hg) is not used here. The elevation is from 99.63∘C to 100∘C.
✓ Quick Checklist to Avoid Errors
| Step | What to check |
|---|---|
| ΔTb | Subtract correctly: final − initial |
| Kb | Use water's value: 0.52 |
| Mass of solvent | Convert g → kg |
| Molality formula | m=KbΔTb |
| Moles of solute | =m×kg solvent |
| Mass of solute | =moles×molar mass |
| Rounding | Keep 4 decimals, round only at end |
Final tip: Always write the formula first, then plug in numbers with units. This catches most errors before they happen. Good luck!
- TG EAPCET 2025Set eng-2025-05-03-AN1 markMCQQ.Temperature of maximum density of H2O is y K and D2O is x K. (x−y) (in K) is nearly (A) 7.0 (B) 3.5 (C) 4.0 (D) 8.5
›Reveal solutionSolution
The key idea is that the temperature of maximum density for water isotopes shifts due to isotopic mass differences; D₂O has its maximum density at about 11.2 °C (284.35 K) and H₂O at 3.98 °C (277.13 K), so the difference is roughly 7.2 K, making option (A) 7.0 the closest.
Concept and intuition
Most liquids become denser as they cool, but water is famously anomalous: it reaches its maximum density at about 4 °C, not at its freezing point. This happens because of the balance between thermal contraction and the open, hydrogen-bonded structure that forms as water approaches freezing. For heavy water (D₂O), the stronger deuterium bonds shift this balance to a higher temperature. The difference in these maximum-density temperatures is what we need.
Step-by-step reasoning
- Recall the known values
- For ordinary water (H₂O), the temperature of maximum density is well known:
Tmax(H2O)=3.98∘C≈4∘C
In Kelvin:y=273.15+3.98=277.13 K
- Find the corresponding value for heavy water (D₂O)
- Heavy water’s maximum density occurs at a higher temperature because D₂O forms stronger hydrogen bonds (due to the greater mass of deuterium), so the open structure persists to higher temperatures.
- The accepted experimental value is:
Tmax(D2O)≈11.2∘C
In Kelvin:x=273.15+11.2=284.35 K
- Compute the difference
x−y=284.35−277.13=7.22 K
- Match to the given options
- The options are 7.0, 3.5, 4.0, and 8.5.
- 7.22 K is closest to 7.0 K.
Watch outA common mistake is to confuse the freezing point (0 °C for H₂O, 3.82 °C for D₂O) with the temperature of maximum density. They are different — the maximum density is always above the freezing point.
TipA quick memory aid: heavy water’s maximum density is about 11 °C, light water’s is about 4 °C, so the difference is roughly 7 K. This is a standard fact in physical chemistry.
✓Final answerThe correct option is (A).
ANSWER: A
- Recall the known values
- TG EAPCET 2025Set eng-2025-05-03-FN1 markMCQQ.Temperature of maximum density of H2O is y K and D2O is x K. (x−y) (in K) is nearly (A) 8.5 (B) 7.0 (C) 3.5 (D) 4.0
›Reveal solutionSolution
The key idea is that the temperature of maximum density for water isotopes shifts due to isotopic mass differences; D₂O has its maximum density at about 11.2 °C (284.35 K) and H₂O at 3.98 °C (277.13 K), so the difference is roughly 7.2 K, making option (B) 7.0 the closest.
Why this approach works
The temperature of maximum density of water is a well-known physical property: for ordinary H₂O it is 3.98 °C. For heavy water (D₂O), the stronger hydrogen bonds (due to the greater mass of deuterium) shift the density maximum to a higher temperature. The difference arises from isotopic effects on molecular vibrations and hydrogen-bond strength. Instead of deriving from first principles, we recall the accepted experimental values: D₂O’s density maximum occurs near 11.2 °C. Converting to Kelvin and subtracting gives the answer.
Step-by-step reasoning
- Recall the known value for H₂O The temperature of maximum density for ordinary water (H₂O) is 3.98∘C. In Kelvin:
y=3.98+273.15=277.13 K
- Recall the known value for D₂O Heavy water (D₂O) has its maximum density at about 11.2∘C (the exact value is often cited as 11.2 °C or 11.23 °C). In Kelvin:
x=11.2+273.15=284.35 K
- Compute the difference
x−y=284.35−277.13=7.22 K
- Match to the closest option The options are 8.5, 7.0, 3.5, and 4.0. 7.22 is nearest to 7.0.
TipA quick mnemonic: H₂O max density at ~4 °C, D₂O at ~11 °C → difference ~7 K. No need for precise decimals in a multiple-choice context.
Watch outA common mistake is to forget that the temperature of maximum density is not 0 °C or 4 °C exactly for D₂O — some might guess 4 °C for both, giving zero difference. Always use the known experimental shift.
✓Final answerThe correct option is (B).
ANSWER: B
- TG EAPCET 2022Set eng-2022-07-19-AN1 markMCQQ.Which of the following substances show the highest colligative properties? (A) 0.1M BaCl2 (B) 0.1M AgNO3 (C) 0.1M urea (D) 0.1M (NH4)3PO4
›Reveal solutionSolution
Colligative properties depend on the number of particles in solution, not their identity. The substance that dissociates into the most ions will show the highest colligative effect. Here, 0.1M (NH4)3PO4 gives the most particles (4 ions per formula unit), so it wins.
Colligative properties — like boiling point elevation, freezing point depression, and osmotic pressure — depend only on the number of solute particles in a given amount of solvent. That’s the core idea. So when you compare equimolar solutions (all at 0.1M), the one that breaks into the most ions in water will have the highest effective particle concentration, and therefore the strongest colligative effect.
Let’s check each option.
- 0.1M BaCl2 Barium chloride dissociates fully in water:
BaCl2→Ba2++2Cl−
That’s 3 ions per formula unit. So the total particle concentration is 0.1×3=0.3M.
- 0.1M AgNO3 Silver nitrate dissociates:
AgNO3→Ag++NO3−
That’s 2 ions per formula unit. Particle concentration: 0.1×2=0.2M.
-
0.1M urea
Urea is a covalent, non-electrolyte. It does not dissociate at all. So it remains as 1 particle per molecule. Particle concentration: 0.1M.
-
0.1M (NH4)3PO4
Ammonium phosphate dissociates:
(NH4)3PO4→3NH4++PO43−
That’s 4 ions per formula unit. Particle concentration: 0.1×4=0.4M.
Watch outA common mistake is to forget that (NH4)3PO4 gives three ammonium ions, not one. Count the subscript carefully: the ammonium ion appears three times.
Comparing the particle concentrations:
- Urea: 0.1M
- AgNO3: 0.2M
- BaCl2: 0.3M
- (NH4)3PO4: 0.4M
The highest is 0.4M, from ammonium phosphate.
✓Final answerThe substance with the highest colligative properties is 0.1M (NH4)3PO4, option (D).
- TG EAPCET 2021Set ap-2021-08-09-FN1 markMCQQ.Which one of the following graphs correctly represents change in freezing point as a function of solute concentration? (In each graph Tf is plotted on the y-axis against molality m from 0 to 0.1 on the x-axis.) (A) [FIGURE] A straight line with positive slope — Tf increases linearly with m (B) [FIGURE] A straight line with negative slope — Tf decreases linearly with m (C) [FIGURE] A curve falling steeply from a high value and then flattening out (hyperbolic decay) as m increases (D) [FIGURE] A curve that is flat at low m and then rises steeply (exponential-type increase) as m increases
›Reveal solutionSolution
Freezing point depression obeys ΔTf=Kfm, so the freezing point itself falls linearly with molality: Tf=Tf∘−Kfm. The graph is a straight line with negative slope — option (B).
The concept first: why does a solute lower the freezing point?
A liquid freezes at the temperature where the vapour pressure of the liquid equals the vapour pressure of the solid.
- Dissolve a non-volatile solute in the solvent. The solute particles occupy part of the surface, so fewer solvent molecules escape — the vapour pressure of the solution falls (Raoult's law).
- The vapour pressure of the pure solid solvent is unaffected.
- So the two curves — solution and solid — now intersect at a lower temperature. That new intersection is the solution's freezing point.
- Hence: the freezing point of a solution is always lower than that of the pure solvent, and the more solute you add, the lower it goes.
Because the effect depends only on the number of solute particles, not on their identity, freezing-point depression is a colligative property.
Step-by-step derivation of the graph
- Experiment and thermodynamics both give
ΔTf∝m⟹ΔTf=Kfm
where m is the molality and Kf the cryoscopic constant (a fixed property of the solvent — for water, Kf=1.86 K kg mol−1).
- By definition,
ΔTf=Tf∘−Tf
where Tf∘ is the freezing point of the pure solvent and Tf that of the solution.
- Substitute:
Tf∘−Tf=Kfm
Tf=Tf∘−Kfm
-
Compare with the equation of a straight line, y=c+(slope)x:
- Variable on the y-axis: Tf
- Variable on the x-axis: m
- Intercept at m=0: Tf∘ — the pure solvent's freezing point (a positive, finite value)
- Slope: −Kf — a negative constant
-
Therefore the plot of Tf against m is a straight line that starts at Tf∘ and descends uniformly as molality increases. It is linear (not curved) because Kf does not change with concentration in the dilute range shown (m=0 to 0.1).
Testing each graph
- (A) Straight line, positive slope — would mean adding solute raises the freezing point. Contradicts the depression. ✗
- (B) Straight line, negative slope, starting from a finite value at m=0. ✓ Matches Tf=Tf∘−Kfm exactly.
- (C) A curve (hyperbolic decay). The direction is right but the shape is wrong — the relation is strictly proportional, hence linear. ✗
- (D) A rising curve — wrong direction and wrong shape. ✗
✓Final answerThe freezing point falls linearly with molality, so the graph is a straight line of negative slope.
ANSWER: B
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