Standardizing A Solution of Sodium Hydroxide Revised PDF
Standardizing A Solution of Sodium Hydroxide Revised PDF
Standardizing A Solution of Sodium Hydroxide Revised PDF
08/30/19 Page 1 of 6
Materials Chemicals
250 mL Erlenmeyer flask Magnetic Stirrer
Solid sodium hydroxide, NaOH
Weighing Dish Stirring bar
Solid potassium hydrogen phthalate
Balance Wash bottle
Phenolphthalein
50mL burette Ring Stand
Pipet pump Utility clamp
Burette clamp 250 mL beaker
100 mL graduated cylinder
Sodium M.W: 40.00 g/mol Causes severe skin burns and Dispose in
Hydroxide Form: pellets eye damage. Harmful to aquatic liquid
NaOH Color: white life. Material is extremely aqueous
pH:13.0 - 14 destructive to the tissue of the solution
Melting point:318 °C mucous membranes and upper waste
Boiling point:1,390 °C respiratory tract. Wear container.
Density 2.1300 g/cm3 protective gear: goggles, lab
coat, gloves.
If in eyes: Rinse cautiously
with water for several minutes.
Procedure
Before lab procedure, obtained safety wear materials such as googles, lab coat, and gloves.
Obtained a 250 mL Erlenmeyer flask and 100 mL graduated cylinder and measured 100 mL of
distilled water in the graduated cylinder. Poured the 100 mL of distilled water in the Erlenmeyer
flask. Measured 0.435g NaOH on the balance and placed the NaOH inside the flask of distilled
water. Swirled the flask until the solid NaOH completely dissolved. Obtained a 250 mL beaker
and used the same 100 mL graduated cylinder to measure 50 mL of distilled water. Poured the 50
mL of distilled water in the 250 mL beaker. In the first trial, measured 0.510g of KHP on the
balance and poured the KHP in the beaker filled with distilled water. Obtained a magnetic stirrer
and stirring bar. Placed the beaker with KHP solution on top of the magnetic stirrer and added the
stirring bar in the solution. Mixed the solution until the solid KHP completely dissolved. After the
KHP dissolved, added three drops of phenolphthalein. Swirled the beaker to mix the
phenolphthalein into the solution. Obtained a 50 mL buret and rinsed the buret with distilled water
three times. With a 5.0 mL pipet, rinsed the buret with 5 mL portion of NaOH solution through
the tip of the buret and disposed the used NaOH solution in a 250 mL waste beaker. Obtained and
set up ring stand and buret clamp. Used a funnel and filled the buret with 50.0 mL of NaOH
solution. Placed the beaker filled with KHP solution under the buret and slowly drained the NaOH
out the buret drop by drop. While titrating the KHP solution, allowed the magnetic stirrer to run
so the KHP is constantly being mixed. Continued adding NaOH solution in the KHP solution until
the KHP solution turned a faint pink and waited for 30 seconds. The solution remained a light pink
which indicated the end point of the titration. The amount of NaOH solution used to neutralize the
KHP was 22.10 mL. Repeated the titration two more times. The second trial measured 0.514g
KHP and had an end point of 24.25 mL. The third trial measured 0.511g KHP and had an end point
of 25.00 mL. After the trial, cleaned up the lab station and disposed the NaOH and KHP solution
in the liquid aqueous waste container in the fume hood.
Data
Trial 1 Trail 2 Trail 3
Mass of KHP 0.510 g 0.514 g 0.511g
Final NaOH Buret Reading 22.10 mL 24.25 mL 36.62mL
Initial NaOH Buret Reading 0.00 mL 0.00mL 11.81mL
Volume of NaOH used (End Point) 22.10 mL 24.25 mL 24.81mL
Table #2: Standardization of NaOH with KHP
CHEM 1102: Experiment 03 Alexya Rosas
08/30/19 Page 4 of 6
Data Analysis
• Moles of KHP used to neutralize the NaOH solution.
Trail 1: 0.00250 moles of KHP
Trail 2: 0.00252 moles of KHP
Trial 3: 0.00250 moles of KHP
Calculation on Appendix C.
• Molarity of NaOH solution.
Trial 1: 0.113M NaOH
Trail 2: 0.104M NaOH
Trail 2: 0.101M NaOH
Calculation on Appendix D.
• Comparison of experimental molarity of NaOH with the theoretical 0.10M.
The first trial had a 0.113M concentration and was the most far off the theoretical
value of 0.10M with a 13% error. The second trial is closer to 0.10M than the first with a
0.104M concentration and 4.0% error. The third trail gave the best results with a 0.101M
concentration and 1.0% error to the goal of 0.10M.
Analysis/ Discussion/ Conclusion
The purpose of this lab is to determine the concentration of NaOH solution by titration it with a
standard solution of known concentration. The standard solution used for this lab was
KHP. During the titration, the stoichiometric ratios between NaOH and KHP are met and the
endpoint is reached when the acid turned from colorless to light pink. The end point tells the
volume needed of the unknown concentration, NaOH. Once the volume of NaOH is found, with
stoichiometric ratios the number of moles of KHP is used to find the concentration of NaOH. This
lab consisted with three different trials. The first trial measured 0.510g of KHP and had an end
point of 22.10 ml of NaOH; having a 0.113M NaOH. With the experimental value of 0.113M and
the theoretical value of 0.10M the percent error calculated is 13%. The first trial had the most
amount of error and this is due to putting excess NaOH causing the end point volume to be higher
than it should be. In the second trial measured 0.514g of KHP and had an endpoint at 24.25 mL of
NaOH; having a 0.104M NaOH. With the experimental value of 0.104M and the theoretical value
of 0.10M the percent error is 4.0%. The second trail was closer towards the goal of 0.1M however,
there is a small amount of error. A source of error during this trail could have been incorrectly
measuring an accurate amount of solid KHP, this would have caused the calculation yield more
moles of NaOH than what actually is. In the third trial measured 0.511g of KHP and an endpoint
of 24.81 mL of NaOH; having a 0.101 M NaOH. The third trial is the most accurate and precise
result out of all the three with only a 1.0% error. The small amount of error could have been from
the equipment since, the lab was done two times with the same materials before the third trail there
could have been excess KHP remaining in the beaker causing to affect the concentration of KHP.
Another source of error could be from the excess base when the titration has reached the endpoint.
CHEM 1102: Experiment 03 Alexya Rosas
08/30/19 Page 5 of 6
Since the indicator only reacts with excess base, a small error is introduced in the titration. As the
data shows an increase in precision and accuracy within each trial. Therefore, its highly
recommend to perform the experiment until there’s a constant concentration of NaOH with each
trial to make sure the concentration of NaOH is correct. From this lab, it can also be concluded
that with the technique of titrations the molarity of a solution of unknown concentration can be
calculated by finding the end point with another solution with known molar quantity.
Appendix
Appendix A: Calculation of grams need to make NaOH of solution.
1𝐿 0.10 𝑚𝑜𝑙 𝑁𝑎𝑂𝐻 40.00𝑔 𝑁𝑎𝑂𝐻
100 𝑚𝑙 𝑜𝑓 𝑁𝑎𝑂𝐻 𝑥 𝑥 𝑥 = 0.4𝑔 𝑜𝑓 𝑁𝑎𝑂𝐻
1000 𝑚𝑙 1𝐿 𝑚𝑜𝑙 𝑁𝑎𝑂𝐻
Trial 2:
1 𝑚𝑜𝑙 𝐾𝐻𝑃 1 𝑚𝑜𝑙 𝑁𝑎𝑂𝐻
0.514𝑔 𝐾𝐻𝑃 𝑥 𝑥 = 0.00251677 𝑚𝑜𝑙𝑒𝑠 𝑜𝑓 𝑁𝑎𝑂𝐻
204.23 𝑔 𝐾𝐻𝑃 1 𝑚𝑜𝑙 𝐾𝐻𝑃
0.00251677 𝑚𝑜𝑙𝑒𝑠 𝑁𝑎𝑂𝐻
= 0.104𝑀 𝑁𝑎𝑂𝐻
0.02425 𝐿 𝑜𝑓 𝑁𝑎𝑂𝐻 𝑠𝑜𝑙𝑢𝑡𝑖𝑜𝑛
Trial 3:
1 𝑚𝑜𝑙 𝐾𝐻𝑃 1 𝑚𝑜𝑙 𝑁𝑎𝑂𝐻
0.511𝑔 𝐾𝐻𝑃 𝑥 𝑥 = 0.002502081 𝑚𝑜𝑙𝑒𝑠 𝑜𝑓 𝑁𝑎𝑂𝐻
204.23 𝑔 𝐾𝐻𝑃 1 𝑚𝑜𝑙 𝐾𝐻𝑃
0.002502081 𝑚𝑜𝑙𝑒𝑠 𝑁𝑎𝑂𝐻
= 0.101𝑀 𝑁𝑎𝑂𝐻
0.02481 𝐿 𝑜𝑓 𝑁𝑎𝑂𝐻 𝑠𝑜𝑙𝑢𝑡𝑖𝑜𝑛