ChemWiki: The Dynamic Chemistry E-textbook > Physical Chemistry > Physical Properties of Matter > Solutions and Mixtures > Colligative Properties > Anomolous Colligative Properties

- 1. Introduction
- 2. Resources
- 3. Contributors

**Anomalous Colligative Properties** are: colligative properties that deviate from the norm, they are irregular and inconsistent colligative properties. Chemist Jacobus van't Hoff was the first to describe anomalous colligative propereites, but it was Svante Arrhenius who succeded in explaning anomalous values of colligative properties.

- 1. Introduction
- 2. Resources
- 3. Contributors

To better understand anomalous colligative properties there should be a knowledge of what Colligative Properties are: **Colligative properties** are the properties of solutions that rely only on the number(concentration) of the solute particles , and **not** on the identity/type of solute particles, in an ideal solution. There is a direct relationship between the concentration and the effect that is recorded. Therefore, Colligative properties are helpful fin analyzing the nature of a solute after it is dissolved in a solvent.

Examples of Colligative properties are: vapor pressure lowering, freezing point depression boiling point elevation osmotic pressure

With that said, there are some solutes that produce a greater effect on colligative properties than what is expected. Arrhenius explained this by using the following equation:

\(\Delta{T_f} = -K_f \times m = -1.86 \; ^{\circ}C \; m^{-1} \times 0.0100 \; m = -0.0186 \; ^{\circ}C\)

The expected freezing point for this solution would be: - 0.0186 \(^{\circ}C\). Lets say that this solution was that of urea, the measured freezing point is close to -0.0186 \(^{\circ}C\). If it were to be a solution of NaCl, then the measured freezing poing would then be -0.0361 \(^{\circ}C\). According to Van't Hoff the factor, \(i\) is the ratio of the measured value of a colligative property to that of the expected value if the solute is a nonelectrolyte. Now, for 0.0100 *m* NaCl, it would be:

\(i = \dfrac{measured \; \Delta{T_f}}{expected \; \Delta{T_f}}\)

For the solute urea \(i\) = 1. For a strong electrolyte like NaCl that produces 2 moles of ions in a solution/ mole of solue dissolved, the effect on the freezing point depression would be expected to be twice as much as that for a nonelectrolyte. The expected \(i\) = 2.

This leads to equations be rewritten as follows:

Original | Rewritten |

\(\pi = M \times RT\) | \(\pi = i \times M \times RT\) |

\(\Delta{T_f} = -K_f \times m\) | \(\Delta{T_f} = -i \times K_f \times m\) |

\(\Delta{T_f} = -K_b \times m\) | \(\Delta{T_f} = i \times K_b \times m\) |

We can just substitue 1 for \(i\) for nonelectrolytes and for strong electrolytes, find the value of \(i\). ( Petrucci)

- Petrucci, Harwood, Herring, Madura. General Chemistry, Principles & Modern Applications 9th Edition. Upper Saddle River, NJ: Pearson Education, Inc., 2007.
- Zumdahl, Steven S. Chemistry 4th Edition. New York: Houghton Mifflin,1997.

- Nathalie Interiano (UCD)

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