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SAMPLE OF A FORMAL LAB REPORT

Follow this format meticulously whenever you are asked to turn in a formal lab report.

Chem 122 Name: John Brown


Section CM1 Name of Partner: Jane Smith
Spring 2007 Instructor: Dr. J. Lyvinski
Date of Expt: 2/3/07
Date of Submission: 2/10/07

Experiment #17:
DETERMINATION OF THE CONCENTRATION OF
AN AQUEOUS SOLUTION OF HCl

Note to Students: The Cover Page should contain nothing else. Begin a new page for
the next section. Remember not to split a table over two pages. Abstract is in bold.

Abstract: Concentration of an aqueous solution of HCl was determined by titrating it


with a solution of NaOH of known concentration. NaOH solution was slowly added to
the HCl solution until a faint pink color persisted for 30 seconds. The molarity of the
HCl was then calculated based on the volume and molarity of the NaOH solution and
volume of HCl solution used in the titration. Three trials were performed and the
average concentration was found to be 0.1475 M with an average deviation of 0.07%.

Introduction: The concentration of an unknown solution of HCl was to be determined.


This was done by titrating a sample of the HCl solution against a solution of NaOH of
known concentration. The reaction involved is as follows:
HCl (aq) + NaOH (aq) H2O (l) + NaCl (aq)
Phenolphthalein was used as the indicator, which changes from colorless when acidic to
pink when basic. With the HCl solution in the flask with the phenolphthalein, the solution
would be colorless initially. When just enough of the NaOH solution has been added to
neutralize the HCl solution, the solution would change to a pale pink. This is the endpoint
of the titration. It is close to the stoichiometric point, where the number of moles of HCl
that were present in the flask is equal to the number of moles of NaOH added. By
measuring the volume of the NaOH solution needed to neutralize the HCl solution, and
noting the concentration of the NaOH solution, the number of moles of NaOH added to the
flask can be calculated. At the end point, this is also the number of moles of HCl, and in
conjunction with the volume of HCl solution used, the molarity of the HCl solution can be
calculated.

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Experimental Section
Equipment/Material: Buret, 25-mL volumetric pipet, 250-mL Erlenmeyer flasks (three),
ring stand, clamp, phenolphthalein, standard 0.1000 M NaOH solution, HCl solution of
unknown concentration, magnetic stir bar and stir plate

Procedure: The procedure described by Hamilton et al.1 was followed, with the
exception that four trials were performed instead of three. The results of Trial #2 are not
included in the calculations because the endpoint was too pink. Below is a brief outline of
the procedure.

Using a pipet, 25.00 mL of the unknown HCl solution #159 was transferred into an
Erlenmeyer flask. Three drops of phenolphthalein indicator was added. A standard 0.1000 M
NaOH solution was placed in a buret, and the initial buret reading was recorded. The NaOH
solution was added dropwise until the solution turned a pale pink that persisted after 30
seconds of stirring. The final buret reading was recorded. The color at the endpoint was
recorded. The above steps were repeated for three additional trials.

Data & Observations:


HCl Unknown # = 159
Volume of HCl solution used in each titration = 25.00 mL
Concentration of NaOH solution = 0.1000 M

Trial # #1 #2 #3 #4
Final Buret Reading of NaOH 35.38 mL 36.90 mL 36.26 mL 35.81 mL
Initial Buret Reading of NaOH 0.10 mL 1.12 mL 1.06 mL 0.55 mL
Volume of NaOH soln used 35.28 mL 35.78 mL 35.20 mL 35.26 mL
Color at endpoint pale pink bright pink pale pink pale pink

Calculations & Results:


Calculations & Results pages are attached. Below is a set of Sample Calculation for
Molarity of HCl using data in Trial #1:
# moles of NaOH at endpoint =
0.1000 mol NaOH
MxV x (0.03528 L NaOH soln) 0.003528 mol NaOH
1 L NaOH soln
# moles of HCl at endpoint = # moles of NaOH at endpoint = 0.003528 mol HCl

molarity of HCl of Trial #1 = # moles of HCl / volume of HCl solution


0.003528mol HCl
0.1411mol/L 0.1411M HCl
0.02500L HCl soln

Average molarity of HCl based on Trials #1, 3 & 4 =

2
( 0.1411 0.1408 0.1410) M
0.1410M
3

Deviation of the molarity obtained in Trial #1 from the Average =


experimental value average value = 0.1411 M 0.1410 M = 0.0001 M
Average deviation of the Trials #1, 3 & 4 =
(0.0001 + 0.0002 + 0.0000) M
0.0001 M
3
Relative Average Deviation of the Three Trials =
Average Deviation 0.0001M
x 100 x 100 0.07 % deviation
Average Molarity 0.1410 M

Discussion of Results:
Concentration of an unknown HCl solution was determined by titrating it with a NaOH
solution of known concentration. The table below shows the results from the three trials
calculated in the manner shown above.

Trial # #1 #3 #4 Average
Concentration of HCl 0.1411 M 0.1408 M 0.1410 M 0.1410 M
Deviation from Average 0.0001 M 0.0002 M 0.0000 M 0.0001 M*
*Average of the deviations of the three trials.

Relative Average Deviation is 0.07% deviation. The low deviation is an indication that
the concentration reported here is reliable.

Four trials were run. However, trial #2 was discarded because the endpoint was much too
pink. In addition, the volume of NaOH solution needed to bring it to the endpoint was much
larger than the others. A decision was made to perform a 4 th trial in place of Trial #2.

When the result of Trial #2 is discarded, the relative average deviation is only 0.07%, which
shows that the precision is quite good.

The correct molarity for the HCl solution is not known and therefore the accuracy of the
titrations cannot be ascertained. However, with such good precision, and the fact the color
at the endpoints of the three trials were all very pale pink show that it is highly likely the
results are quite accurate.

One of the likely sources of error in this experiment would be in pipeting exactly 25.00 mL
of the unknown HCl solution into each Erlenmeyer flask. It was not easy controlling the
level of the HCl solution in the pipet. This source of error can affect the calculated molarity
of the HCl both ways. If less than 25.00 mL was actually delivered, it would have taken less
NaOH to neutralize the solution, and therefore the calculated molarity of HCl would be too
low. If more than 25.00 mL was delivered, then the calculated molarity of HCl would be
too high.

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A second likely source of error would be in the process reaching the correct endpoint. It
was not easy to control how much NaOH solution to add to reach the pale pink endpoint. If
the end point is too pink, that would mean too much NaOH was added (as was the case in
Trial #2). It would seem that there is more HCl in the flask than is actually there. This
would make the molarity of HCl too high.

Conclusion: The concentration of Unknown # 159 has been determined to be 0.1411 M


HCl, based on three trials, with a relative average deviation of 0.07%. Based on the low
average deviation, the concentration being reported can be considered reliable.

References:
1. Hamilton, P., Zaman K., Yau, C. CHEM 122 Experiments in General Chemistry I
Laboratory; Academx: Bel Air, VA, 2013; pp 315-319.

Answers to Post-Lab Questions:


1. Why can we not stop the titration when the first pale pink appears without waiting for 30
seconds?
If we stop the titration as soon as the first pale pink appears without waiting for 30
seconds of swirling, we would not know whether it is pink because we have truly
reached the endpoint, or whether the HCl and NaOH have not had time to finish
reacting.

2. Why can we not swirl for much longer than 30 seconds to see whether we have reached
an endpoint?
If the pink goes away after having swirled it much longer than 30 seconds, we would not
know whether the pink disappeared because we have not reached the endpoint yet, or
whether it is due to the CO2 absorbed from the air during the prolonged period of
swirling. Carbon dioxide when dissolved in water produces a small amount of carbonic
acid as shown in the equation below. As an acid it can be competing with the HCl in the
reaction with NaOH.
CO2 (g) + H2O (l) H2CO3 (aq)

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