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How to Determine the Molecular Weight of a Non-Volatile Solute

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Methods for Calculating Molecular Weight of Non-Volatile Solutes

The determination of molecular weight of non volatile solute is essential in chemistry for identifying unknown compounds and understanding solution behaviors. Non-volatile solutes, by definition, do not evaporate easily, making their molecular mass measurable through changes they induce in certain physical properties of solvents. This article clearly explains the concepts, methods, and calculations involved in determining the molecular weight or molar mass of non-volatile solutes using various colligative property-based techniques.


Understanding Non-Volatile Solutes and Colligative Properties

A non-volatile solute does not produce significant vapor pressure, so its presence in a solvent directly affects the solvent’s physical properties. The core principle behind the determination of molecular weight of non volatile solute is that the change in properties like boiling point, freezing point, or osmotic pressure depends solely on the concentration (not the nature) of the solute particles. These changes are called colligative properties.


Key Colligative Properties Used in Molecular Mass Determination

  • Relative lowering of vapor pressure: Measures the decrease in solvent’s vapor pressure due to added solute.
  • Elevation of boiling point (Ebullioscopy): The solvent's boiling point increases in the presence of a non-volatile solute.
  • Depression of freezing point (Cryoscopy): The solvent’s freezing point drops upon solute addition. This is widely used for the determination of molecular weight by freezing point depression.
  • Osmotic pressure: The increased osmotic pressure can also be used to determine molecular masses, especially for large molecules and polymers.

Freezing Point Depression Method (Cryoscopic Method)

Cryoscopy, or the freezing point depression method, is a reliable way to find the molecular weight of a non-volatile solute. The central equation is:

$$ \Delta T_f = i \times K_f \times m $$

Where:

  • $\Delta T_f$ = freezing point depression
  • $i$ = van’t Hoff factor (number of particles produced per molecule)
  • $K_f$ = cryoscopic constant of the solvent
  • $m$ = molality of solution


Molality is determined as:
$ \mathrm{molality} = \dfrac{\mathrm{moles\ of\ solute}}{\mathrm{mass\ of\ solvent\ (kg)}} $
For molecular mass ($M$):
$ \mathrm{molality} = \dfrac{\mathrm{mass\ of\ solute}}{M \times \mathrm{mass\ of\ solvent\ (kg)}} $


By rearranging, the molecular mass of solute can be found:
$ M = \dfrac{\mathrm{mass\ of\ solute}}{\mathrm{molality} \times \mathrm{mass\ of\ solvent\ (kg)}} $


Variants of Freezing Point Depression Methods

  • Rast Method: Utilizes naphthalene as the solvent to determine the molecular mass of a non-volatile solute by observing the extent of freezing point reduction.
  • Beckmann’s Method: Employs precise thermometry to measure small changes in freezing or boiling points for accurate molar mass calculations.

Other Common Techniques

Beyond freezing point depression, several other methods are available to determine molecular weight of non volatile solute:


  • Elevation of Boiling Point (Ebullioscopy): Uses similar formulas as cryoscopy with the boiling point elevation constant ($K_b$) instead of $K_f$.
  • Osmotic Pressure Method: Especially suitable for large molecules, polymers, and proteins. This technique calculates molecular mass from osmotic pressure ($\Pi$) as:
    $ \Pi = iCRT $
    Where $C$ is molarity, $R$ is the gas constant, $T$ is temperature (in Kelvin), and $i$ is the van’t Hoff factor.
  • Victor Meyer Method: Traditionally used to find the molar mass of volatile liquids, not non-volatile solutes, but helpful for comparison.
  • Relative Lowering of Vapor Pressure: Applies Raoult’s Law for non-volatile solutes:
    $ \dfrac{P^0 - P}{P^0} = X_{solute} $

Raoult’s Law Derivation for Non-Volatile Solutes

  • Raoult's Law states that the relative lowering of vapor pressure is equal to the mole fraction of the solute, forming the basis for calculating molecular mass.
  • Abnormal molar mass can occur if solutes associate or dissociate in solution; the van't Hoff factor ($i$) corrects for this.

Summary Table: Colligative Methods at a Glance

  • Freezing Point Depression (Cryoscopy): Accurate for most non-volatile solutes; Rast’s and Beckmann’s methods are practical variants.
  • Boiling Point Elevation (Ebullioscopy): Used similarly with boiling point changes.
  • Osmotic Pressure: Preferred for polymers/macromolecules due to ease and accuracy.
  • Vapor Pressure Lowering: Useful for dilute solutions under Raoult’s Law.

For a deeper understanding of solution properties and molecules, you can explore topics like properties of fluids or Avogadro’s number and its significance. These foundational concepts are closely related to solution chemistry and calculations.


Additionally, learning about kinetic theory of gases and concentration measurements can deepen your grasp on how particle numbers influence physical properties.


In summary, the determination of molecular weight of non volatile solute via colligative properties such as freezing point depression, boiling point elevation, osmotic pressure, and vapor pressure lowering is a foundational analytical tool in chemistry. Each method, whether it’s the determination of molecular mass of a non volatile solute by Rast method or through Beckmann’s freezing point approach, relies on measuring how a solute alters solvent properties proportionally to the amount of dissolved particles. Correct application of these techniques reveals the molar mass and structure of unknown substances, reinforcing essential chemical principles and aiding practical research. Mastery of these methods equips students and researchers to analyze solution behavior confidently and accurately.


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FAQs on How to Determine the Molecular Weight of a Non-Volatile Solute

1. What is the method to determine the molecular weight of a non-volatile solute?

The molecular weight of a non-volatile solute can be determined using the method of elevation in boiling point (ebullioscopy) or depression in freezing point (cryoscopy). Both these colligative property-based methods follow these steps:

  • Prepare a solution by dissolving a known mass of the non-volatile solute in a known mass of solvent.
  • Measure the change in boiling or freezing point of the solution compared to the pure solvent.
  • Apply the formula for the relevant colligative property to calculate the molecular weight (molar mass) of the solute.

2. How is the molecular mass of a non-volatile solute calculated using the depression in freezing point?

The molecular mass of a non-volatile solute is calculated using the depression in freezing point (ΔTf) by employing the formula:

  • M = (1000 × Kf × w2) / (ΔTf × w1)
Where:
  • Kf = molal depression constant of the solvent
  • w2 = mass of solute (g)
  • w1 = mass of solvent (g)
  • ΔTf = depression in freezing point (°C)

3. What is a non-volatile solute? Give an example.

A non-volatile solute is a substance that does not easily vaporize and has a negligible vapor pressure compared to the solvent.

  • Examples include sugar (glucose), urea, and common salt (NaCl).
  • These solutes do not evaporate, making them suitable for colligative property determinations.

4. Why are non-volatile solutes used to determine molecular mass using colligative properties?

Non-volatile solutes are used because they do not contribute their own vapor pressure, ensuring that changes in colligative properties reflect only the presence of the solute.

  • This allows for accurate calculation of molecular mass using properties like boiling point elevation, freezing point depression, and osmotic pressure.

5. What are the colligative properties used for determining molecular mass?

The four main colligative properties used for determination of molecular mass are:

  • Relative lowering of vapor pressure
  • Elevation in boiling point (ebullioscopy)
  • Depression in freezing point (cryoscopy)
  • Osmotic pressure
These properties depend on the number of solute particles, not their nature.

6. Write the formula for calculating molecular weight using elevation in boiling point.

The formula for molecular weight determination using elevation in boiling point (ΔTb) is:

  • M = (1000 × Kb × w2) / (ΔTb × w1)
Where:
  • Kb = molal elevation constant of solvent
  • w2 = mass of solute (g)
  • w1 = mass of solvent (g)
  • ΔTb = elevation in boiling point (°C)

7. What precautions should be taken while determining the molecular mass of a non-volatile solute in a laboratory experiment?

While determining molecular mass in the lab, observe these precautions:

  • Use pure solvent and non-volatile solute only.
  • Accurately measure all masses and temperatures.
  • Avoid contamination of the solution.
  • Ensure complete dissolution of the solute.
  • Constantly stir the solution for uniform temperature.
Such care increases the accuracy of the results.

8. How does presence of impurities affect the determination of molecular mass by colligative properties?

Impurities can significantly alter the colligative property measurements, thus affecting the calculated molecular mass:

  • Any additional solute particles increase the change in boiling/freezing point.
  • This results in a lower calculated value of molecular mass.
  • It is crucial to use pure chemicals for correct results.

9. What is cryoscopy and how is it related to molecular mass determination?

Cryoscopy is the method of determining the molecular mass of a solute by measuring the depression in freezing point of a solvent when the solute is dissolved in it.

  • The greater the depression (ΔTf), the more solute particles present.
  • By using the standard formula, the molecular mass of the non-volatile solute can be calculated.

10. Explain why molecular mass obtained by colligative properties may differ from the theoretical value.

The molecular mass obtained by colligative properties can differ from the theoretical value due to:

  • Association or dissociation of solute in the solvent (e.g., acetic acid dimerizes in benzene, NaCl dissociates in water).
  • Presence of impurities.
  • Experimental errors in temperature, mass measurement, or incomplete dissolution.
Always consider the van't Hoff factor (i) in such cases to correct the calculation.