Solve ΔTb = i · Kb · m to find how much a dissolved solute raises a solvent's boiling point — a colligative property that depends only on particle count, not identity. Compute the elevation directly, find the new boiling point, or explore how the van't Hoff factor changes the result.
Inputs
Moles of solute per kilogram of solvent (mol/kg).
Number of particles the solute dissociates into. Nonelectrolytes: 1. NaCl-type: 2. CaCl₂-type: 3.
Solvent-specific constant, in °C·kg/mol. Water = 0.512.
Common solvents (sets Kb)
Result
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Enter molality, the van't Hoff factor, and Kb to compute the boiling point elevation.
Inputs
The pure solvent's boiling point at 1 atm, in °C. Water = 100.
Moles of solute per kilogram of solvent (mol/kg).
Number of particles the solute dissociates into.
Solvent-specific constant, in °C·kg/mol.
Result
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Enter the normal boiling point, molality, the van't Hoff factor, and Kb to compute the new boiling point.
Boiling point elevation—
Solute dissociation
Moles of solute per kilogram of solvent (mol/kg).
Solvent-specific constant, in °C·kg/mol. Water = 0.512.
Ideal particle count. Real solutions dissociate slightly less than ideal at higher concentration.
Solute type (sets i)
Result
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Enter molality, Kb, and a van't Hoff factor to see how dissociation changes the elevation.
4 min read3 steps7 terms3 examples6 FAQsΔTb = i · Kb · m
Dissolving anything in a liquid raises its boiling point — a small but measurable effect called boiling point elevation.
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Walk-through
How to Use This Calculator
3 steps▸
1
Enter molality, the van't Hoff factor, and Kb
On the Elevation tab, enter the solution's molality (moles of solute per kilogram of solvent), the van't Hoff factor i (how many particles the solute splits into), and the solvent's ebullioscopic constant Kb. Water's Kb is 0.512 °C·kg/mol — use the preset chip or look up another solvent's value.
2
Read the elevation
The result card shows ΔTb, the temperature increase over the pure solvent's boiling point. Switch to the New Boiling Point tab and add the solvent's normal boiling point to see the actual boiling temperature of the solution.
3
Compare solute types
Use the van't Hoff tab to see how dissociation changes the result: a nonelectrolyte like sugar (i=1) produces half the elevation of a 1:1 salt like NaCl (i=2) at the same molality, and a third of a 1:3 salt like AlCl₃ (i=4).
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Reference
Formula & Methodology
2 formulas▸
Boiling point elevation
ΔTb = i · Kb · m
ΔTb is the boiling point elevation in °C. i is the van't Hoff factor — the number of particles one formula unit of solute produces in solution (1 for nonelectrolytes like sugar, 2 for NaCl, 3 for CaCl₂, 4 for AlCl₃, assuming complete dissociation). Kb is the solvent's ebullioscopic constant in °C·kg/mol (0.512 for water). m is the molality of the solution in mol/kg.
New boiling point
Tb(solution) = Tb(solvent) + ΔTb
The solution's actual boiling point equals the pure solvent's normal boiling point plus the elevation. For water (100 °C) with a 1 molal NaCl solution (i=2), the new boiling point is 100 + (2 × 0.512 × 1) = 101.024 °C.
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Glossary
Key Terms Explained
7 terms▸
Boiling point elevation ↗The amount a solvent's boiling point rises when a solute is dissolved in it, denoted ΔTb and measured in °C or K. It is always positive — dissolving a solute always raises the boiling point.
Colligative property ↗A property of a solution that depends only on the number (concentration) of dissolved particles, not on their chemical identity. Boiling point elevation, freezing point depression, vapor pressure lowering, and osmotic pressure are the four classic colligative properties.
Molality (m) ↗Moles of solute per kilogram of solvent (mol/kg). Unlike molarity, molality does not change with temperature because it is defined by mass, not volume — which is why it is the concentration unit used in colligative-property formulas.
van't Hoff factor (i) ↗The number of individual particles one formula unit of solute produces when it dissolves. Nonelectrolytes (sugar, ethanol) stay as single molecules, so i=1. Ionic compounds dissociate: NaCl → Na⁺ + Cl⁻ gives i=2; CaCl₂ → Ca²⁺ + 2Cl⁻ gives i=3. Real solutions show slightly lower effective i than the ideal value at higher concentrations due to ion pairing.
Ebullioscopic constant (Kb) ↗A property specific to each solvent that scales how strongly its boiling point responds to dissolved particles, in °C·kg/mol. Water's Kb is 0.512; other solvents like camphor (5.95) or benzene (2.53) are far more sensitive to the same molality.
Dissociation ↗The separation of an ionic compound into its constituent ions when dissolved in a solvent. Complete dissociation is assumed by the ideal van't Hoff factor; incomplete dissociation (common in concentrated solutions) lowers the effective i below its ideal value.
Solute ↗The substance being dissolved into the solvent to form a solution — the salt, sugar, or other compound whose molality and van't Hoff factor drive the boiling point elevation.
ΔTb = 2 × 0.512 × 1 = 1.024 °C. Because NaCl fully dissociates into two ions, it produces twice the elevation of a nonelectrolyte at the same molality — the new boiling point is 101.02 °C.
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Home cook
Salting pasta water
Molality ≈0.1 mol/kg (a tablespoon of salt per liter)van't Hoff factor (i) 2Kb (water) 0.512 °C·kg/mol
At typical cooking concentrations, ΔTb ≈ 0.1 °C — far too small to noticeably speed up cooking. Salting pasta water is about seasoning the pasta itself, not raising the boiling point in any useful way.
ΔTb = 1 × 0.512 × 3 = 1.536 °C. Sugar doesn't dissociate, so despite the high molality the elevation is still modest — candy thermometers track much larger boiling-point shifts as water boils off and molality keeps climbing.
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Reference
Cite This Calculator
APA & MLA▸
Use either format to cite this calculator in a paper, report, or resource list.
Dissolving anything in a liquid raises its boiling point — a small but measurable effect called boiling point elevation. It's one of four colligative properties, meaning it depends only on how many particles are dissolved, not on what they are. This calculator applies the standard formula ΔTb = i·Kb·m to find the elevation and the resulting boiling point for any solute-solvent combination.
How the formula works
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Adding solute particles to a solvent lowers the solvent's vapor pressure at any given temperature, because solute particles occupy some of the surface where solvent molecules would otherwise escape into vapor. A liquid boils when its vapor pressure equals the surrounding atmospheric pressure, so a solution with lower vapor pressure needs a higher temperature to reach that same threshold — hence the elevation.
The relationship ΔTb = i·Kb·m captures this exactly: more dissolved particles (higher i or higher m) means a bigger vapor-pressure suppression and a bigger elevation. The proportionality constant Kb is empirically measured for each solvent and folds in the solvent's molar mass and enthalpy of vaporization.
Inputs and what they mean
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Molality (m) is used instead of molarity because it doesn't shift with temperature — the mass of solvent stays fixed even as the solution's volume changes slightly with heat. The van't Hoff factor (i) is the input most people get wrong: it's not the number of atoms in the solute, it's the number of independent particles it splits into in solution. Table sugar (sucrose) stays intact, so i=1; table salt splits into two ions, so i=2. Kb is solvent-specific — water's value of 0.512 °C·kg/mol is the one worth memorizing, since it appears in nearly every textbook problem.
Limits and edge cases
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The ideal van't Hoff factor assumes complete dissociation, which holds well at low, dilute concentrations but breaks down as concentration rises — ions start re-pairing (ion pairing), so the effective i drops below the ideal integer value. For precise work at high concentrations, use an experimentally measured i rather than the theoretical value. The formula also assumes the solute is non-volatile (it doesn't itself evaporate and contribute vapor pressure) — for volatile solutes like alcohol in water, this simple model doesn't apply and Raoult's law for mixed volatiles is needed instead.
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Questions
Frequently Asked Questions
6 questions▸
What is the formula for boiling point elevation?+
ΔTb = i · Kb · m, where i is the van't Hoff factor (particles per formula unit), Kb is the solvent's ebullioscopic constant (°C·kg/mol), and m is the molality of the solution (mol/kg).
What is Kb for water?+
Water's ebullioscopic constant is 0.512 °C·kg/mol. Other common solvents have much larger constants — benzene is 2.53, camphor is 5.95 — meaning the same molality produces a bigger boiling point shift in those solvents.
Does salting pasta water actually make it boil at a higher temperature?+
Technically yes, but the effect is tiny. A typical tablespoon of salt in a few liters of water raises molality only slightly, producing an elevation of a small fraction of a degree — nowhere near enough to meaningfully speed up cooking. Salt is added to pasta water mainly for flavor.
What does the van't Hoff factor mean?+
It's the number of individual particles one unit of solute breaks into when dissolved. Sugar and other molecular compounds stay intact (i=1). Ionic compounds dissociate into their ions: NaCl gives 2 particles (i=2), CaCl₂ gives 3 (i=3), and AlCl₃ gives 4 (i=4), assuming complete dissociation.
What units does the calculator use?+
Molality is in moles per kilogram (mol/kg), the ebullioscopic constant is in °C per kg per mole (°C·kg/mol), the van't Hoff factor is unitless, and boiling points and the elevation are both in °C.
How is boiling point elevation different from freezing point depression?+
They're mirror-image colligative properties driven by the same vapor-pressure-lowering effect: dissolved solute raises the boiling point (elevation, positive ΔTb) but lowers the freezing point (depression, negative ΔTf) of the same solution. The formulas have the identical shape (ΔT = i·K·m), just with the solvent's cryoscopic constant (Kf) instead of Kb for freezing point depression.
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