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Setting volumetric analysis pratical
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Introduction/purpose: The purpose of this lab was to find the concentration and mass volume percent of acetic acid in different brands of vinegar solution. In order to find the concentration and mass volume percent of acetic acid we performed a volumetric analysis. This means that the vinegar solution was neutralized by adding a base solution. To view this neutralization process phenolphthalein indicator was added. Phenolphthalein indicator will turn slightly pink when the solution is neutralized. Materials: • 0.05 M of Sodium Hydroxide solution (NaOH) • Vinegar (Acid “A” and Acid ”B”) • Phenolphthalein indicator • Two 150ml beakers • 50ml Burette • Three 250ml Erlenmeyer flasks • 10ml pipette and pipette bulb • Wash bottle • Funnel • Retort stand and clamps Procedure: 1. Clamp the 50ml burette to the retorted stand and add the sodium hydroxide solution (base) using a funnel. 2. Clean one of the Erlenmeyer flasks using a wash bottle and add 10ml of Acid “A” into it. Use the pipette to accurately measure 10ml before adding it to the flask. 3. Add 2-3 drops of phenolphthalein indicator into to the Erlenmeyer flask containing the Acid “A”. 4. Place the Flask under the burette that is filled with the Sodium Hydroxide (base). 5. The Solution inside the burette was unveiled slowly and mixed together with the Acid “A”. The flask was swirled continuously to ensure the Sodium Hydroxide is thoroughly mixed. 6. Stop the flow of the base when the Acid ‘A’ changes it color to light pink. 7. Repeat the process again with the second batch of Acid ‘A’ and record the results. 8. Repeat the process using Acid B and record the results. Result To neutralize 10 mL of Acid ‘A’ we used 3.35 mL of Sodium Hydroxide and to neutralize 10 mL of... ... middle of paper ... ...etic acid than Acid ‘A’. The amount of Base that took to neutralize Acid ‘A’ was 3.9 mL while Acid ‘B’ was 3.5 mL. Finally, the concentration of Acetic acid in Acid ‘A’ was 0.017 mol/L and Acid ‘B’ was 0.19 mol/L Error Analysis: Our titration lab went smooth, however there were some errors that can be identified. One such error was that we added too much Sodium Hydroxide during the titration. This could have had a negative effect in the data we gathered and the calculations. Giving us a slightly inaccurate measurements. This can be avoided by getting used to the burettes release mechanism and knowing how to control the flow of the Sodium Hydroxide to the Acid. Conclusion: To conclude this lab, we learned how to calculate the mass volume percent of acetic acid in a vinegar solution using stoichiometry learned in unit 2 and how to conduct a proper titration lab.
...ost likely to be battery acid. If it is water, it has a Ph level of around 7. For vinegar, the Ph level is approximately 2.4 - 3.4. Thus, once testing the liquid compare it with the Ph levels above to discover the mystery solution.
== Volume of NaOH used is recorded below: Trial (cm3) 1st time (cm3) Initial burette reading 3.55 18.4 Final burette reading 22.8 36 Titre 19.25 17.6 pH Chloroethanoic acid 3.0 Dichloroethanoic acid 2.2 Ethanoic acid 4.6 pH of chloroethanoic acid and dichloroethanoic acid is given by the teacher. Calculation: = ==
Then, I added 8 drops of concentrated phosphoric acid to the mixture. swirling it a few times. Then, I carefully took the flask to the station as I avoided trying to breath the vapors of the acetic anhydride. I put the e-flask into the beaker of water sitting on the hot plate in order to heat it for seven minutes. Once the seven minutes was up, my partner carried the e-flask to the fume hood, and added 3 mL of de-ionized water to the flask. She swirled it for a couple of minutes there. She brought it back tot he station where I gradually added 60 Ml of de-ionozed water to the mixture while my partner stirred the mixture constantly. I was able to see some of the aspirin beginning to form. In order to complete the crystallization process we cooled the flask in an ice-water bath from 4:00 until 4:20. As we waited I began to set up our filtration system. I used a ring stand, right angel clamp, three finger clamp, Buchner funner, filtering flask,rubber tubing, and filter paper in the Buchner funnel. I turned on the aspirator and pored some water over the filtering paper in order to create a good
Apparatus: * 1 measuring cylinder * 1 test tube * 1 stop clock * A large gelatine cube containing indicator and NaOH * Hydrochloric acid ranging from 1-3 molars * A scalpel Diagram: Method: * Take the large gelatine cube and cut into 15 equal pieces * Place on piece of the cube into the test tube * Measure out 10mls of HCl in the measuring cylinder * Pour the HCl into the test tube with the gelatine cube and start the clock * Time how long it takes for the pink colour inside the gelatine cube to completely disappear * You will also notice that the cube dissolves slightly * Record your results and repeat this same process 3 times for each molar of acid: § 1 molar § 1.5 molar § 2 molar
The reaction will take place in the conical flask from where the gas produced will travel into the up-turned measuring cylinder. The gas will then displace the water in the tube. I will measure out exactly 50ml of 1molar hydrochloric acid into the conical flask. I will then weigh out exactly or as close as possible to 2 grams of small sized marble chips.
alkali. First we set up the burette. We placed it into a clamp so that
2. Step 2: Heat the mixture: Make sure the agarose dissolves. Wait until it boils and when you are going to transfer the mixture, wear gloves to avoid getting burnt. Transfer the mixture to a removable gel tray. 3.
Pour 1.40g of NaOH into florence flask and add 350ml distilled water, then swirl it and invert flask five times with parafilm on the top of it. Next, obtained a vial of KHP from the instructor, and poured about 0.408g into three different Erlenmeyer flasks by measuring with analytical balance. Then, fill up about 25ml of distilled water, add 3 drops of phenolphthalein into it and mix them well with a glass rod. Label all solutions to prevent mixing them up. Before the titration began, the buret should be rinsed with NaOH solution and recorded the initial buret reading.
Four drops of the unknown liquid (L21) or 50mg of solid unknown (S21) is mixed with 2mL of water in a test tube. 2mL of 3M sodium Hydroxide was then added. 3mL of iodine solution was added. The results of the reaction were
Normal water will not do because of the impurities in it. · Methyl Orange indicator - The colour of this indicates when the sodium hydroxide has been neutralised by the hydrochloric acid. · Conical Flask - This is used to react the aspirin tablets with the sodium hydroxide. It is more appropriate to use as the shape of it makes it less likely that any should spill out. · Burette - This is used to add the hydrochloric acid to the sodium hydroxide.
Despite straining the lemon juice before titration, small amounts of pulp would have affected the titrations, because pulps was in some cases blocking the pipette when the juice is transformed from volumetric to conical flask. For future investigation, instead of straining the lemon juice, it could have been filtered to remove all pulp and thus increase the accuracy of the result
Rinse the buret with two, 5 mL portions of the NaOH solution. Fill the buret with the NaOH solution and expel any air bubbles. Empty excess liquid into a 50 mL beaker.
borate) and 1.0 g. of sodium hydroxide in 20 mL of warm water. It may
The theoretical numbers were vastly different from measured results, this may be due to calculation errors. The concentration both upstream and downstream were also very similar.
In this experiment the Sodium Hydroxide solution went through three different phases where its quality and quantity changed. The first phase was called I. Preparing Approximately 0.1M NaOH, 1000mL of clear distilled water was boiled and then chilled to room temp.