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Chemistry 101 lab
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Recommended: Chemistry 101 lab
Objective: Making alum called potassium aluminum sulfate dodechydrate, from aluminum and potassium hydroxide. Materials: Aluminum foil weighing 1.0254 g ripped into small pieces, 250 mL beaker, Buchner funnel, filter paper, graduated cylinder, 25 Ml of 3 MKOH solution, Stirring rod, 35 Ml of sulfuric acid, 50 Ml of Aqueous ethanol solution. Procedure: we started this experiment by gathering aluminum foil, in the lab manual it does not clearly state how small the piece of foil need to be, so we cut them into about the size of tomato’s diced. The total weight of our foil was 1.024 g. Placed into a 250 mL beaker and 25 mL potassium hydroxide solution added with the foil. Once the solution was added we noticed a large amount of heat, and gas coming …show more content…
off the solution until finally the aluminum was dissolved. The solution at this point looked like gray water, and had a few little chucks of foil not broken up. In order to solve this, we then ran solution through the Buchner funnel twice and not the one recommended time in the lab manual. Once we ran the solution through the filter a second time we finally reached the desired color, of being clear. Next the lab manual advised to allow the solution to cool to room temperature, we waited a totally of 3 minutes but the solution was still slightly warmed when we continued. Sulfuric acid was then added to the solution and total of 35.5 mL and stirred constantly.
While the sulfuric acid was, being added we noticed a milky clump start to form, better known as precipitate but once the sulfuric acid was added completely instead the solution was thicker and cloudy white, sort of like the early starts of mashed potatoes. Our solution still had larger clumps of product so we decided to do the optional piece placed into our lab manual, which is filter the solution again to remove the clumps out. Once we filtered the solution for the total of 3 times during this lab we found that we had roughly 58 mL of solution left. This solution we took and placed on a hot plate to a slow boil until we reached 50 mL left the beaker. We then allowed the beaker to cool to room temperature and placed the beaker into the ice bath. During the ice bath, we ran into some issues after the 15 minutes had passed we had hardly any crystal formation, so by the advice of the professor we scraped the bottom and the sides of the beaker and left the beaker in the ice bath for an additional 10 minutes. Finally, we poured the crystal through a filter and poured 50 mL of ethanol solution over the crystals. Data: In the start of this lab we used aluminum foil weighing 1.0254 g, and the final weight of the product, 2KAl(SO4)2 * 12H20 + 3 H2 , was an actual yield of 6.3281 g. Once we finished this process we calculated the molar mass to find out the theoretical yield and the percent yield,
the molar mass of KAl(SO4)2 * 12H20 was 474.41 grams. Once having the molar mass was continued to find a theoretical yield of 18.03 grams, making our percent yield 35.09 %. Results: The final product produced was a lot less than our class mates given use only 35.09 %, we wondered if this could have been a series of mistakes such as filter more than recommend, not waiting for the product to reach room temperature or the issue in the ice bath in which the crystals themselves were having issues forming. The final product was a crystal soft substance that was white like snow, with an overall glitter appearance to it. Conclusion: The fact that the percent yield was so low was a disappointment for me and my partner we both discussed what could have went wrong during the lab to produce such as low amount of product, the best idea we came up with was an issue with the heating process its self, because we filtered so many times we had little solution to boil, leading us to believe this was the reason for the low crystal production. References:
The purpose for this lab was to use aluminum from a soda can to form a chemical compound known as hydrated potassium aluminum sulfate. In the lab aluminum waste were dissolved in KOH or potassium sulfide to form a complex alum. The solution was then filtered through gravity filtration to remove any solid material. 25 mLs of sulfuric acid was then added while gently boiling the solution resulting in crystals forming after cooling in an ice bath. The product was then collected and filter through vacuum filtration. Lastly, crystals were collected and weighed on a scale.
Each subsequent trial will use one gram more. 2.Put baking soda into reaction vessel. 3.Measure 40 mL vinegar. 4.Completely fill 1000 mL graduated cylinder with water.
Repeat for each trial. Rinse volumetric pipette with vinegar and drain into the waste beaker. Weigh and record the mass of each 200mL beaker. Add 10.00mL of vinegar into each beaker and weigh them and record their again. Add 50mL of de-ionized water to the beakers and place them under the drop counter on top of a stir plate, submerging the pH meter into the solution. Place the stir bar into the beaker and carefully turn on the stir plate so that the stir bar spins without splashing or hitting the sides of the beaker or the pH
The 100% theoretical yield should be 0.059 grams of myristic
To assemble this apparatus all of the following will be needed: a jacketed condenser, thermometer, 50 mL kjeldahl shaped flask, 100 mL kjeldahl flask, vacuum adapter, distilling column and a connecting adapter. Next, clamp the glass joints to the ring stand to properly secure the apparatus. Once finished with assembly, proceed to ad 60 mL of the fermented yeast prepared at the last experiment lab to the 100 mL flask and also add a small spin vane. Then, carefully place the flask into the sand bath. After this is done, let the water run that’s connected to the condenser slowly. At the same time, also slowly heat up the solution. For the experiment to be the most successful it’s important to slowly heat the flask because properly heating the flask will lead to a high percentage purity ethanol distillation. You can also add aluminum foil to the bottom of the flask, as this will help with the reflux process. Keenly observe the reflux process as you continue to slowly heat up the solution. Once the reflux line starts to get nearer to the connection adapter, record the temperatures. Once there’s a good amount of distillate in the 50 mL flask, go ahead and collect 2 to 3 mL of the distillate and transfer this into a labeled vial and give to your TA so he/she can measure out the distillate using a 1000 mL Eppendorf pipette. Lastly, weigh the solution on an analytical balance and record the weight. Using the weight recorded, calculate the density and compare to the density table listed below to determine the percent
While completing this lab we used four liquids. We used water, milk, orange juice, and soda. To hold the liquids we used two q-tips. We used two petri dishes, one was to hold the pill bugs while they were not being used in the
I blended on high to make the potatoes more liquid-like. I grabbed the cheesecloth and placed on the top of the blender. I poured the potato extract on the container and labeled it. I found out that I have to make 1% sugar solution so I grabbed the sugar and measured into 5 grams on the scale. I added 5 grams of sugar on 250 ml graduated cylinder and poured the water into the cylinder. I mixed the sugar with water and poured it into the saucepan. I refilled the water into the graduated cylinder and poured into the saucepan. I turned on the heat of the stove and saw the sugar dissolved. I poured into a container and labeled 1% sugar solution. I repeated the same thing with 1% salt solution by using 1 gram of salt and filled the water into graduated cylinder by 100 ml. I answered question three. In the first experiment, I grabbed four transfer pipets and used it to put solutions into the test tubes by 3ml. I labeled it and placed into the plastic cups so it can stand upright. I grabbed each test tube and poured 2 ml of catalase solution into it. I also tapped and swirled to measure the bubbles by using the ruler. I wrote the numbers into the lab report. In the second experiment, I labeled the room
8. Continue stirring. Record the temperature at which crystals begin to appear in the solution.
== Refer to, Chemistry Lab #1 – What’s the substance? However, I changed some of procedures during my experiment, here is the changes I made in this experiment: * I only used the toothpick to place a small amount of each sample on a separate piece of paper, instead of the spatula.
of distilled water. For the 1M solution I added 50 cm3 of HCl and 50
2. In the large beaker, put water and boil it completely. After that, remove the beaker from heat. 3. Sample tubes (A-D) should be labeled and capped tightly.
Add 15mL of 6N sulfuric acid to a 125mL Erlenmeyer flask containing 105mL of deionized water (preparing approximately 0.75N sulfuric acid). Obtain a sample of the unknown. Weight the vial and contents accurately on an analytical balance. Handle the vial with a small strip of paper to reduce the risk of error (due to added weight). Pour about half of the sample into a clean dry 200mL Erlenmeyer flask and weight again. Use the remaining half of the sample to get a second weight of around 0.6g-0.7g. Make sure the vial is capped on every weight taken.
== § Test tubes X 11 § 0.10 molar dm -3 Copper (II) Sulphate solution § distilled water § egg albumen from 3 eggs. § Syringe X 12 § colorimeter § tripod § 100ml beaker § Bunsen burner § test tube holder § safety glasses § gloves § test tube pen § test tube method = == = =
Analysis: This experiment is divided into two parts. In the first part; the standardized solution of sodium hydroxide is prepared by titrating it with base Potassium hydrogen phthalate (KHP). Phenolphthalein (range 8.3 to 10.0) is used as indicator to determine whether the titration is completed.
0.1M HCl, 10 mL of 0.1N KMnO4, 0.2 g. KI, 5 mL of alcohol, and 5 mL of