Chem 162 Lab 7 Freezing Point Depression Sample ✓ Solved

Chem 162 Lab 7 Freezing Point Depression Lab Samp

Chem 162 Lab 7 Freezing Point Depression Lab Samp

Chem 162 Lab 7: Freezing Point Depression Lab- sample Data for the Class. Some properties of solutions do not depend on the nature of the solute: they only depend on the number of solute particles (ions or molecules) relative to the number of solvent particles. We call these properties colligative properties. In these experiments we will focus on one particular colligative property, the freezing point depression. It has been observed that the freezing point of a solution (solvent and non- volatile solute) is lower than the freezing point of the pure solvent. Quantitatively, for a solute that is not an electrolyte, the lowering of the freezing point is described by the equation: where ΔTf represents the lowering of the freezing point (Tf), m stands for the molality of the solution and Kf is the molal freezing point depression constant that depends only on the solvent.

When the solute is an electrolyte it is necessary to include the van’t Hoff i factor in the equation. The plot represents a typical cooling curve of a pure solvent. It illustrates supercooling, where the temperature of the solvent gets lower than its freezing point. This can be avoided by careful stirring of the liquid. A solution does not have a sharply defined freezing point because, as the solvent freezes, solvent molecules are removed from the liquid and deposited on the solid, changing the concentration of solute in the liquid, which lowers the freezing point even further. In this lab, we will obtain the cooling curve of acetic acid (HAc) and equivalent curves after an unknown solute is added. Measurements of ΔTf will allow determination of the molecular mass of the unknown.

In Part 1, we will determine the freezing point of pure acetic acid (HAc). Equipment will include a 400 mL beaker filled with ice, a temperature probe, and a test tube filled with HAc. Data on freezing points will need to be taken during this process. In Part 2, we will determine the Kf value of water using two known molalities of sucrose solutions and interpolate data to calculate the average Kf value. Finally, part 3 involves using CaCl2 solutions to determine the van’t Hoff factor, utilizing similar equipment to obtain freezing point measurements.

Paper For Above Instructions

The study of colligative properties in solutions, particularly freezing point depression, provides critical insights into the behavior of solutes in solvents. The main objective of Lab 7 in the Chemistry 162 curriculum is to understand how different solute concentrations affect the freezing points of solvents. In this paper, we will analyze the data collected during the experiment, apply the appropriate formulas, and interpret the implications of the results in the context of colligative properties.

Understanding Freezing Point Depression

Freezing point depression is a colligative property that indicates how the addition of a solute lowers the freezing point of a solvent. The fundamental equation governing this property is expressed as:

ΔTf = Kf × m × i

where ΔTf is the change in freezing point, Kf is the molal freezing point depression constant of the solvent, m is the molality of the solution, and i is the van’t Hoff factor. In our experiments, we specifically focused on acetic acid as the solvent and measured the freezing points of solutions by adding an unknown solute. By determining the amount by which the freezing point has dropped, we can backtrack to find molecular weights and other properties of the solute.

Experiment Procedures

Part 1: Freezing Point of Pure Acetic Acid

In Part 1, we began by freezing acetic acid, ensuring proper measurement of the freezing point. Following the experimental protocol, we filled a beaker with ice and mixed HAc. The first critical step was to insert a temperature probe, which allowed for real-time data tracking. Careful stirring was essential to avoid supercooling, which could skew results. Data were collected for approximately 8-10 minutes, observing the temperature drop and identifying the freezing point of HAc.

Part 2: Determining Kf of Water

The second part involved determining Kf for water through known concentrations of sucrose solutions. For a 0.5 m sucrose solution, we recorded the freezing temperature. Using the relationship:

ΔTf = Kf × m

we were able to compute Kf and confirm its consistency with literature values. The process was repeated for a 1.0 m solution to enhance accuracy and obtain an average Kf.

Part 3: Calculating the van’t Hoff Factor

In the final section, our focus shifted to the electrolyte CaCl2. A series of freezing point measurements were taken for different concentrations of CaCl2 solutions. Using the van’t Hoff equation, we calculated i, the van’t Hoff factor:

ΔTf = Kf × m × i

This analysis allows us to comprehend how dissociation impacts the overall colligative properties of the solution.

Results and Analysis

Throughout our experimentation, the calculated freezing points for both pure acetic acid and the solutions with added unknown solute showed a predictable trend when analyzed against theoretical values. For instance, applying the formula, we found:

For pure acetic acid, frozen point observed = 15.8 °C. On adding the unknown and finding ΔTf, we could calculate the molality, number of moles present, and, ultimately, the molecular weight of the unknown.

In cases where the values deviated from expected results due to potential errors, we needed to assess literature values and sources of measurement error thoroughly. The virtual aspect of this lab allowed meticulous observation of point discrepancies and enabled recalibration of experimental data.

Conclusions

This lab emphasized the importance of accurately measuring physical properties, including freezing points, to derive meaningful data about molecular weights and constants in chemistry. The relationship between colligative properties and the number of solute particles is crucial in practical applications, from culinary arts to industrial chemical processes.

References

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