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Freezing Point Depression Lauric Acid 4/21/2011 Tootoonchi FY Thien Tran

Freezing Point Depression

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Freezing Point Depression

Freezing Point DepressionLauric Acid

4/21/2011Tootoonchi FYThien Tran

Introduction

When a substance freezes or solidifies, the molecules come into a certain arrangement. In some cases, the molecules become closely packed to form a very dense solid [1]. If impurities are present, more energy is used to solidify the substance, which lowers the freezing point of the substance. The equation was used to determine the freezing point depression constant (Kf) where T is the lowering of the freezing point in C and m is molality. Molality is moles solute/mass solvent. Molality is used instead of molarity because volume (which is used in molarity) is dependent on temperature whereas mass is not. Thus, a changing the temperature will not change the molality in this case. The purpose of this experiment was to determine the value of the freezing point depression constant for Lauric acid. To find the freezing point depression of Lauric acid, the melting point was determined twice for pure Lauric acid and once each for 2 mixtures of Lauric acid and different amounts of benzoic acid. Using the experimentally determined values for the change in the melting point and the molality of the samples, it was possible to find the freezing point depression constant and take an average to determine the final value.

Procedure

First, a 400 mL beaker was filled with approximately 400mL of water and placed a the hotplate until a temperature of about 60-70 degrees was reached while another 400 mL beaker with room temperature water was placed to the side. Then, the LoggerPro apparatus and the interface were connected to the computer and started. After the water reached the desired temperature, a test tube containing pure Lauric acid was placed into the heated water bath until the entire sample had melted. Once the Lauric acid had completely melted, the test tube was removed from the hot water bath and the temperature probe was placed in the test tube and we began to stir. After about 5 seconds, the test tube was then placed into the other beaker and the data collection was started. The acid was stirred until the temperature of the Lauric acid stopped decreasing and leveled out. In order to continue the temperature decrease, ice cubes were added to the beaker of water.To determine the freezing point we highlighted to flat portion of the graph and found the line of best fit for the temperature vs. time graph. The y intercept of the linear fit line was the freezing point. Then, the data was saved and stored and a new run was set up. The procedure was performed again with the same sample of pure Lauric acid. After each run, it was necessary to place the test tube with the temperature probe back into the hot water bath to allow the Lauric acid to melt so we could take out the temperature probe. Then probe was then rinsed off and dried before using it with other samples.After the first two tests of the pure Lauric acid, the same test was run on two other samples. A test tube that contained 0.75 g of benzoic acid and 8.00 g of Lauric acid was placed into the hot water bath to melt. After it melted, the freezing point was determined the same way it was determined for the pure Lauric acid. Then all the steps were repeated for a solution containing 1.50 g of benzoic acid and 8.00 g of Lauric acid. Using the values for the freezing point from the experiments, we were able to calculate the T and the molality of each solution. Using this information and the equation mentioned in the introduction (), we determined the freezing point depression constant (Kf). The two values were then averaged to find a final value for Kf.

Equations

EquationsVariables:

(1)

(2)

(3)

(4)

(5)

(6)

Data Collection

Mp of pure Lauric Acid 1 (C)43.7Mp of pure Lauric Acid 2 (C)43.45Average Mp for pure Lauric Acid (C)43.58Molecular Weight of benzoic acid (g/mol)122.12Molality of 0.750g BA / 8.00g LA (m)0.768T of 0.750g BA / 8.00g LA (C)1.09Kf determined from 0.750g BA / 8.00g LA (C/m)1.42Molality of 1.50g BA / 8.00g LA (m)1.54T of 1.50g BA / 8.00g LA (C)7.07Kf determined from 1.50g BA / 8.00g LA (C/m)6.01Average Kf (C/m)3.01

Calculations

The molality of the Lauric acid samples were calculated using equation (2).

The average melting point temperature of the pure Lauric acid was calculated using equation (3).

The change in temperature in each sample was determined using equation (4).

The freezing point depression constant was determined using equation (5) and rearranging the terms.

The average freezing point depression constant was calculated using equation (6).

Analysis

How Error Can Be IntroducedError may have been introduced during the cooling of the Lauric acid. While it was solidifying in the beaker of water, the temperature probe was moving around and there may have been an uneven temperature distribution since the acid was cooling from the outside in. Therefore, touching the test tube with the probe may have sent undesired readings to the collection of data. Also, the test tubes were left open to the atmosphere while warming up in the beaker on the hot plate. This may have allowed the solution to evaporate some of its water content.

How This Error Will Change Our ResultIf the temperature probe touched the outside of the beaker and picked up uneven readings for temperature, the graph would have not leveled out nicely. There would be slight bumps on the flat portion that would affect the determination of the y-intercept, skewing the data. The flat section of the graph would have been unreliable and the melting points would have been off. Also, if some of the water had evaporated from the test tube before the data collection began, the molality may have been altered.

How to Prevent This ErrorTo prevent this error in the future, test tube may be placed in a clamp attached to a ring stand, so that it will be steadier and easier to stir. This way, one may only need to worry about handling the probe, rather than keeping the test tube submerged in the beaker at the same time. Also, the test tubes may be heated while having the caps on, preventing any vapor from escaping during the process.

References

[1] Lab manual