Experiment 233 and Experiment 234 2c Standardization of Naoh Solution and Standarization of 0
Experiment 233 and Experiment 234 2c Standardization of Naoh Solution and Standarization of 0
Jordan Fiedor
October 5, 2017
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solution using a 0.1M Sodium Hydroxide solution with standard KHP while practicing
titrations to learn about the acid-base reaction that is occurring. It will determine
the exact or true concentration of a solution. The unit of concentration used in the
solution of HCl by performing a titration. Students will also learn about the
calibration and use of volumetric pipet. In the end, NaCl will be made and a percent
III. Theory: The Standardization of NaOH Solution and Standardization of 0.1 M HCl
Solution labs contain similar concepts. Both solutions are being standardized, which
solution is finding the molarity, which is the moles divided by the total amount of
solution or the volume in liters. An analytical balance was used to measure the mass
of the solute which is very sensitive but accurate. All doors must be closed and
outside movement that creates vibrations must not be present or it can screw up the
weighing process. Then the tare button, which zeros the scale, is used after a
weighing boat is placed on the scale. A 500-mL volumetric flask is used to prepare
the 0.1 M NaOH solution. A volumetric flask has a bulb at the bottom to hold the
majority of solution, and a long neck with a mark of the exact amount of solution
being measured. It has been calibrated to that single, exact volume and no other
volume can or should be taken from that flask. To calibrate a piece of glassware, the
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mass of the volume of solution is found, then the mass to volume relationship is used
to calculate the true or exact volume of solution. A volumetric pipet is also calibrated
for a single volume reading. There is a bulb located in the middle of a long narrow
part and it is also open on both ends. A pipet bulb is placed on one end of the pipet,
and is used to suck water into the pipet, and dispose or release any water that is
currently contained inside the pipet. To suc water up into the pipet, press the “S”
button or part of the bulb, then press the “E” to empty the amount of water that is
needed. The pipet has to be measured to. In order to find the concentration of an
known molarity and one of unknown molarity. A buret, which is a very long narrow
glass tube, is used to very accurately measure liquids. The measurements begin at the
top with zero or any number close to zero, then get higher towards the bottom of the
buret to measure the amount dispensed. The buret contains the unknown solution in
this lab, which is the titrant. An Erlenmeyer flask is placed directly under the buret
containing the titrand, which is the known solution. When performing a titration, find
the exact amount of titrant added when a solution goes from acidic to basic, or the
other way around. In the lab, phenolphthalein is used as the indicator because it is
clear in an acidic solution and pink in a basic solution. The goal is to add just the
right amount of titrant to turn the titrand solution to create a very light pink color. If
too much is added, the color will become very dark pink and other tests will have to
The KHP is the known, acidic titrand and NaOH is the unknown, basic titrant. KHP is a
primary standard, which means it is pure and has a high molar mass. They are commonly
used in acid-base reactions. NaOH is a strong base, but the salt is also hygroscopic. This
means that it can absorb water molecules from the air, leading to inaccuracy results when it is
weighed. The chemical reaction used for the titration in Lab 4 is:
HCl is the acidic titrand and NaOH is the basic titrant. HCl is a very acidic solution.
When it is reacted with a strong base, salt and water are formed as the products of the
reaction.
IV. Procedure:
A clean 500-mL volumetric flask was used to prepare a 500-mL solution of 0.1 M
NaOH. There were calculations in order to determine the certain mass in grams of the
NaOH needed to make the solution, resulting in 2.00 grams of NaOH. The solid of
NaOH was calculated using a scale of 0.1 grams. A small dish was placed on the
scale before the NaOH was added to zero the scale. Next, 2.00 grams of NaOH was
weighed on the balance. The NaOH that was in the small dish was carefully dumped
into the volumetric flask. Around 100-mL of distilled water was poured into the flask
and then swirled until the majority of the NaOH was dissolved. Distilled water was
added again until the flask was about halfway full. The flask was swirled once again
until the NaOH was dissolved and the solution was clear. The volumetric flask was
then filled with distilled water to the fiducial line and checked at eye level. Parafilm
was put on top of the flask to seal it while the flask was held upside down several
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times to make sure there was a complete mixture. The solution of 0.1M of NaOH was
then poured into a plastic bottle and it was labeled with the name of the solution and
number of moles, the date, and the initials of the student and placed into the correct
lab drawer.
To do the titration of NaOH and KHP solutions, three KHP solutions were
created. A weighing dish was placed on a 0.1g balance, and the balance was zeroed.
The three measurements of the KHP that were weighed was, 0.8000 g (sample 1),
0.8001 g (sample 2), and 0.8001 g (sample 3). Three Erlenmeyer flasks were used
from the lab drawer and each were separately labeled with samples 1, 2, and 3.
Sample one of KHP was placed into the flask and labeled with a 1. The same
followed with samples 2 and 3. About 50 mL of distilled water was added to every
one of the Erlenmeyer flasks to dissolve the solid state of KHP. The solution of
NaOH that was made from Part A was poured into the buret. Three drops of
phenolphthalein were added to the solution of KHP in sample 1. The flask was put
underneath the buret and that was the titrand. The solution was titrated by pouring
NaOH from the buret into the flask. When the titrand could be swirled around for
about 15 to 20 seconds and stay pink, the titration had been completed. The same
The 25-mL volumetric pipet was filled with distilled water using the pipet bulb. If
any water was stuck in the inside of the pipet, it was cleaned out with soap and
distilled water multiple times. A clean and dry 50-mL flask with a cork on the top of
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it was weighed before each trial. The masses were recorded to the nearest 0.1 mg or
0.0001 g. In trial 1, the mass of the cork and flask was 35. 0375 g. 300-mL of
distilled water was then added to the 600-mL beaker, and the temperature of the water
was then record. The temperature of the water was 22.2 C. The pipet was filled to
the 25-mL mark and then the distilled water was delivered into the Erlenmeyer flask.
The cork was put into the flask and the mass of the flask, water, and cork were
collectively recorded. The value was 60.1044 g. This process was repeated for one
more trial. The mass of the flask and cork was 35.0575 g. The temperature was again
recorded at 22.2 C. The mass of the flask, water, and cork was 60.0711 g.
To find the exact concentration of the stock solution of HCl, a titration was
experiment 3 was used as the known titrant solution in this experiment. The buret was
conditioned similar to the way the instructor demonstrated and filled using the NaOH
from experiment 3. A clean and dry 250-mL beaker was weighed at 102.3000 mg
before the beaker was labeled. About 100-mL of HCl solution was put into a separate
250-mL beaker. The 25-mL volumetric pipet was used to transfer about 25.121-mL of
HCl solutions into each 250-mL flask. Once again, three drops of phenolphthalein
were added to the flasks before the titration took place. The solution would be titrated
until a light pink color in the solution stayed for about 15 to 20 seconds. Two more
titrations took place the exact same way as the first. The three “apparent” volumes
should agree within +/- 0.05-mL of each other. All three titrations were then poured
into a 250-mL flask where they were initialed and massed. Next, they were placed in
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the fume hood to dry. About three weeks later, the beaker with salt inside of it was
obtained and massed at 102.7013 g in order to find the total amount of NaCl that
V. Data:
Tria Mass of KHP Initial Buret Reading Final Buret Reading Total Volume
l
1 0.8000 g 0.10-mL 40.23-mL 40.13-mL
2 0.8001 g 0.50-mL 40.75-mL 40.25-mL
3 0.8001 g 0.20-mL 40.28-mL 40.08-mL
Trial 1 Trial 2
Buret
1 0.05-mL 24.30-mL 24.25-mL 24.22-mL
2 0.10-mL 24.29-mL 24.19-mL 24.22-mL
3 0.07-mL 24.28-mL 24.21-mL 24.22-mL
Exp. 4: Data Table of Mass of Empty Beaker and Beaker with Salt
VI. Calculations:
Exp. 3: Part A- We need to find the amount of solid NaOH needed to make 500-mL of 0.1 M
NaOH solution
500 mL
( ) (1L) = 0.5L
1000 mL
Second, is to calculate the moles of the solute (NaOH) to make .5L of 0.1 M NaOH solution
by multiplying the Molarity of the solution by the amount of L. The moles of the solute = the
Third, is to convert the moles of NaOH to grams of NaOH by multiplying the number of
Exp. 3: Part B- We need to calculate the Molarity of NaOH for each trial.
Trial 1:
First, is to find the moles of NaOH in the titrated solution by taking the grams of KHP,
converting it to moles, and multiplying it by the ratio found in the chemical equation.
Second, is to convert the mL of NaOH to liters by dividing the amount of the solution by
1000.
1 liter
(40.25mL) ( ) = 0.04025 L
1000 mL
Third, to calculate the concentration of NaOh by dividing the number of moles of NaOH in 1
Trial 2: Repeat the calculations 1, 2, and 3 for the second trial measurements from the
titration.
2. = 0.04013 L NaOH
3. = 0.9761 M NaOH
Trail 3: Repeat the calculations 1, 2, and 3 for the third trial measurements from the
titration.
2. = 0.04008 L NaOH
3. = 0.9775 M NaOH
Exp. 3: Part B- We need to calculate the average Molarity of NaOH from all three trials by
Exp. 4: Part A- We need to calculate the volume of H2O in the pipet by multiplying the mass
mL
Trial 1: (25.0669 g H2O) 1.0032 ) = 25.147 mL H2O
g
mL
Trial 2: (25.0136 g H2O) (1.0032 ) = 25.094 mL H2O
g
Exp. 4: Part A- We need to calculate the average volume of H2O by adding the trial values
and dividing by 3.
Exp 4: Part B- We need to calculate the molarity of the HCl solution by multiplying the
molarity of NaOH from experiment 3 by the total volume of NaOH used to find the moles of
NaOH. Then, we use the ratio of the balanced chemical equation to find the number of
moles of HCl.
First, we need to find the number of moles of HCl by multiplying the molarity of the NaOH
from experiment 3 by the total number of NaOH in liters used to find the moles of NaOH.
Second, the ratio from the balanced chemical equation is used to find the number of moles
1 L mol HCl
(0.002363 mol NaOH) ( ¿=0.002363mol HCl
1mol NaOH
Third, need to convert the amount of HCl in mL to liters by dividing the amount in mL by
1000.
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25.121mL HCl
( ¿ (1 L HCl )=0.025121 L HCl
1000mL HCl
Fourth, we must divide the moles by the volume in order to get the molarity.
Exp. 4: Part B- We use the percent error formula to calculate the percent error compared to
Exp. 4: Part B- We need to calculate the percent yield of NaCl by multiplying the volume in
liters by NaOH by the Molarity of the NaOH to find the moles of NaOH. We would do the
same with HCl so the reaction creates the NaCl. Also, it would show the limiting factor. Then
we use a ratio in the chemical equation to find the number of moles of NaCl. Next, we
multiply it by the molar mass of NaCl to get grams of NaCl. We multiply the NaCl by 3
because there were three trials. Then we subtract the dry beaker from the beaker with salt
to see the number of salt produced. Next, we would take the actual mass and divide by the
1 liter
¿)( )(24.22 mL) = 0.002363 mol NaOH
1000 ml
0.4013 g NaCl
( ¿ ( 100 % )=100.5 %
0.3993 g NaCl
VII. Discussion
Overall, I feel that both experiments that I conducted were successful. My titration
Technique had very little error presented. My titrated solutions turned a dark pink once,
making me believe that the other 3 trials I performed were successful. My percent error
shows that my values were better than most of the class average’s, and my values were
close to the molarity of the HCl solution. My actual yield of NaCl, 0.4013 g was just litter bit
bigger than my theoretical yield at 0.3993 g. This may be because not all the water was
gone when the beaker was weighed. I feel that there is no need to change anything during
my experiments or perform anything else. They instructions were extremely easy and I liked
performing both experiments. Although some students may find titrations difficult because
they make the titration extremely pink, but I feel executing the experiment correctly is a big
part of chemistry, and every student needs to perform them the correct way and improve
themselves as a scientist.
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