Molar Mass Formula:
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This calculator determines the molar mass of a solute using boiling point elevation data. This colligative property method is based on how adding a solute to a solvent raises its boiling point, with the elevation proportional to the molality of the solution.
The calculator uses the formula:
Where:
Explanation: The formula calculates molar mass by relating the boiling point elevation to the molality of the solution, accounting for the dissociation factor of the solute.
Details: Determining molar mass is fundamental in chemistry for identifying unknown compounds, calculating stoichiometric relationships, and understanding molecular properties. The boiling point elevation method provides a practical experimental approach for this determination.
Tips: Enter all values with appropriate units. Ensure the solvent mass is in kilograms. Common K_b values: water (0.512 °C·kg/mol), benzene (2.53 °C·kg/mol), ethanol (1.22 °C·kg/mol). The van't Hoff factor is 1 for non-electrolytes and equals the number of ions produced for electrolytes.
Q1: What is the van't Hoff factor?
A: The van't Hoff factor (i) represents the number of particles a solute dissociates into in solution. For non-electrolytes, i = 1; for electrolytes, it depends on the degree of dissociation.
Q2: Why must solvent mass be in kilograms?
A: The molal boiling point elevation constant (K_b) is defined in °C·kg/mol, so using kg for solvent mass ensures proper unit cancellation in the calculation.
Q3: How accurate is this method?
A: This method provides good estimates for molar mass but works best for non-volatile solutes and when precise temperature measurements are made. Accuracy depends on knowing the correct K_b value and van't Hoff factor.
Q4: Can this method be used for all solvents?
A: Yes, but you need the appropriate K_b value for the specific solvent being used in the experiment.
Q5: What are common sources of error in this calculation?
A: Potential errors include inaccurate temperature measurements, imprecise mass measurements, incorrect K_b values, not accounting for the complete dissociation of electrolytes, and using this method for volatile solutes.