Upload
sharmaine-manahan
View
99
Download
5
Embed Size (px)
Citation preview
Freezing Point Depression: Molecular Weight Determination
Manahan, Sharmaine E.Group 4BS Chemistry III
College of Science and MathematicsWestern Mindanao State UniversityNormal Road, Baliwasan, Zamboanga City
ABSTRACT
In the experiment conducted, the freezing temperature of the mixture of glacial acetic
acid and naphthalene, unknown and glacial acetic acid solution, and pure glacial acetic acid
which is the organic solvent, were measured. It has been observed that when a solute was added
to the solvent, the freezing point of such a solution is lower than that of the pure solvent.
Based on the results gathered, the molecular weight of naphthalene was 125.8 g/mol +
0.41 and for unknown, 61.63 g/mol + 24.4. Thus, the theoretical molar mass of naphthalene is
128.2 g/mol. Since the standard deviation of the molar mass of naphthalene was + 0.41, it means
that there is a small spread of data due to its calculated value which is less than 1. On the other
hand, the molecular weight of the unknown has a standard deviation + 24.4, it implies that the
data obtained was not precise and there is a large spread of data.
The molar mass of the substance was determined, and the freezing point of that solution
to that of pure solvent was able to compare. The data collected was graphed to show how the
solutes affect the freezing point of a substance.
KEYWORDS: Freezing point, Molecular Weight, Temperature, Standard Deviation
INTRODUCTION
Solutions are homogeneous mixtures that contain two or more substances. The major
component is called the solvent, and the minor component is called the solute. Since the solution
is primarily composed of solvent, physical properties of a solution resemble those of the solvent.
Some of these physical properties, called colligative properties, are independent of the nature of
the solute and depend only upon the solute concentration, measured in molality, or moles of
solute per kilogram of solvent. The colligative properties include vapor pressure lowering,
boiling point elevation, freezing point depression, and osmotic pressure. The vapor pressure is
the escaping tendency of solvent molecules. When the vapor pressure of a solvent is equal to
atmospheric pressure, the solvent boils. At this temperature, the gaseous and liquid states of the
solvent are in dynamic equilibrium, and the rate of molecules going from the liquid to the
gaseous state is equal to the rate of molecules going from the gaseous state to the liquid state.
The new freezing point of a solution can be determined using the colligative property
law:
ΔTf = kf m
The change in freezing point is equal to the molal freezing-point constant times the molality of
the solution. The molal freezing-point constant used is the constant for the solvent, not the solute.
In this experiment, the molar mass of sulfur will be determined using the colligative
property law. The freezing point of naphthalene will be determined experimentally; then a
controlled solution of naphthalene and unknown will be made, and the freezing point of that
solution will be determined. The difference in freezing point can be used in the colligative
property law to determine the experimental molality of the solution, leading to a calculation of
molecular weight.
The freezing temperature is difficult to ascertain by direct visual observation because of a
phenomenon called supercooling and also because solidification of solutions usually occurs over
a broad temperature range. Temperature-time graphs, called cooling curves, reveal freezing
temperatures rather clearly.
METHODOLOGY
In this experiment, 5-mL glacial acetic acid, naphthalene, unknown, dewar flask, becky
thermometer, stopwatch, pipette, aspirator, salt for the ice bath, outer and inner freezing point
tubes, and 100-mL beakers were used.
The small dewar flask was filled with ¾ of ice-water mixture. Five mL of acetic acid was
placed into the inner freezing point tube. After doing so, the inner freezing point tube was placed
inside the outer freezing point tube and put in an ice bath. The temperature reading from the
thermometer was recorded every 30 seconds. The solution was stirred up and down to ensure
even freezing. When the temperature remained constant for several readings, the solution was
allowed to cool without further temperature readings. The inner tube warmed with hand until all
the crystals have melted. After this, 0.10-mL of glacial acetic acid was added and the same
technique was applied. Then, 0.05-mL of glacial acetic acid has been added to the acetic acid and
the same procedure was repeated until 0.30-mL of glacial acetic was already added. For
naphthalene and unknown, these solutes were added separately after allowing the solvent to
warm with hands.
RESULTS AND DISCUSSION
Table 1.1 shows the experimental and theoretical weight of different substances with
respect to its constant temperature.
Solution Weight/mL Constant temperature
Molecular weight% ErrorExperimental Theoretical
(naphthalene)
Pure Glacial Acetic acid
5.00 mL + 0.01
14.2oC + 0.01
125.8 g/mol + 0.41
128.2 g/mol 1.87%Naphthalene 0.5080 g -
Pure Glacial Acetic Acid + Naphthalene
- 11.2oC + 0.01
For unknown
Pure Glacial Acetic Acid
5.00 mL + 0.01
14.32oC + 0.01
61.63 g/mol + 24.4
- -Unknown 0.5112 g -
Pure Glacial Acetic acid +
Unknown- 7.52oC + 0.01
The known molar mass of naphthalene is 128.2 g/mol. The calculated molar mass of
naphthalene was 125.8 g/mol + 0.41. A percent error calculation can help to measure the
accuracy of the experiment and it has been found out that the percent error was 1.87%. It
indicates that the experimental molecular weight of naphthalene is accurate due to its small
percentage of error. This error is attributable to several sources of error that were present in this
experiment. While the imprecision of instruments is not technically a source of error, it had a
particularly effect on this experiment. Additionally, the transfer of powdered naphthalene from
the weighing paper to the test tube may have been incomplete. Some particles of naphthalene
may have been lost or may have gone unreacted due to the imperfection of the transfer method.
The standard deviation value which is + 0.41 implies that the experiment conducted was precise
and there is a small spread of data.
The molecular weight of the unknown solution was also determined experimentally. But
the standard deviation gave a value of + 24.4 which means that a large spreading of data was
done. To determine the molar mass of a substance, one must simply divide the grams of
substance by the number of moles of substance present. All of these values were determined
experimentally.
In the figure 1.1, the variation of temperature of pure glacial acetic acid, and solution of
naphthalene with glacial acetic acid was shown graphically with respect to the time interval.
0 100 200 300 400 500 6000
5
10
15
20
25
30
35
f(x) = − 0.0355392156862745 x + 23.6176470588235R² = 0.639161363544242f(x) = − 0.0307692307692308 x + 22.1153846153846R² = 0.616796695731987
Temperature reading vs. TimeTemperature reading (pure Acetic acid)
Linear (Temperature reading (pure Acetic acid))
Temperature reading (Acetic acid with Naphthalene)
Linear (Temperature reading (Acetic acid with Naphthalene))
Time, sec
Tem
pera
ture
Figure 1.1 Reading of Temperature (pure Acetic acid, Acetic acid with naphthalene) vs. Time
The theory associated with this experiment is the atomic theory of matter. The atomic
theory of matter offers explanations for bonding and physical phase. The figure 1.1 presented
above illustrates the difference between pure substance and a solution. The freezing point of a
solution of glacial acetic acid with naphthalene is lower than the freezing point of the pure
substance. Because when a solute is present, the surface of the solution is comprised of solute
particles and solvent particles, instead of only solvent particles. When the vapor pressure of a
solution is lowered, the freezing point is lowered. Because the number of molecules of solute has
a direct effect on the rate of evaporation, the freezing point depression of a solution is
proportional to the molality of the solution.
The same case happened in the unknown substance. When unknown was added into the
pure acetic acid the freezing point decreases than that of pure solvent. To visualize the effect of
the addition of unknown to the solvent, a graph was encapsulated in figure 1.2.
In figure 1.2, the variation of temperature of pure glacial acetic acid, and solution of
unknown with glacial acetic acid was presented graphically with respect to the time interval.
0 100 200 300 400 500 6000
5
10
15
20
25
30
35
f(x) = − 0.040034965034965 x + 20.0641025641026R² = 0.631349075588061
f(x) = − 0.0452380952380952 x + 26.7582417582418R² = 0.817442452501541
Temperature reading vs. TimeTemperature Reading (pure Acetic acid)
Linear (Temperature Reading (pure Acetic acid))
Temperature Reading (Acetic acid with unknown)
Linear (Temperature Reading (Acetic acid with unknown))
Time, sec
Tem
pera
ture
Figure 1.2 Reading of Temperature (pure Acetic acid, Acetic acid with unknown) vs. Time
There are many ramifications associated with this experiment. One is the personal
experience using colligative equations was gained. Also techniques to prevent supercooling were
practiced.
CONCLUSION
In this experiment, the freezing temperature of the pure solvent, glacial acetic acid was
found first. Next, the freezing point of a solution prepared from a mixture of an unknown organic
compound and glacial acetic acid was measured. Also, the freezing point of naphthalene and
acetic acid mixture was assessed too. It is true that the vapor pressure of volatile solvents is
lowered when a non-volatile solute is used to make a solution. The result is that such a solution
has a lower freezing point than that of the pure solvent.
Based on the results obtained, the molecular weight of naphthalene was 125.8 g/mol +
0.41 and for unknown, 61.63 g/mol + 24.4. For comparison, the actual molar mass of
naphthalene is 128.2 g/mol. Since the standard deviation of the molar mass of naphthalene was +
0.41, it implies that there is a small spread of data because it is less than 1. On the other hand, the
molecular weight of the unknown has a standard deviation + 24.4, it implies that the data attained
was not precise and there is a very large spread of data.
The determination of the molar mass of the substance, and the comparison of the freezing
point of that solution to that of pure solvent were achieved. The experiment was not very
accurate, but it was still successful in terms of the original purpose.