Question

I have posted the procedure of the lab below. Please tell me what the theoretical yield...

I have posted the procedure of the lab below. Please tell me what the theoretical yield is for aspirin based on this procedure and explain how you got it. I am not sure I am doing this right.

SYNTHESIS OF ASPIRIN

Procedure:

  1. Start heating a water bath in your 250 mL beaker by filling it with ~150 mL of tap water.

  2. Carefully weigh out 1.0 gram of salicylic acid. Transfer to a 50 mL Erlenmeyer flask.

  3. In the fume hood, add 3.0 mL of acetic anhydride to the flask.

  4. Add 3 drops of phosphoric acid to the flask.

  5. Clamp the flask so that it is in the water bath. Continue heating the water bath to a boil. Stir the contents to dissolve the rest of the salicylic acid, if needed.

  6. Once the water boils, turn off the heat and keep the flask in the water bath for 10 minutes.

  7. After the 10 minutes, leave the flask in the water bath and slowly add ~1 mL of DI water to the flask to decompose any excess acetic anhydride.

  8. After a minute, remove the flask from the water bath and add 10 mL of DI water. Let the flask cool to room temperature. If crystallization has not occurred, scratch the inside of the flask with a spatula to initiate crystallization.

  9. Once crystals have begun to form, cool the flask in an ice bath for 15 minutes or until no more crystals form. Also, chill 10-15 mL of DI water in a small beaker.

  10. Weigh a piece of filter paper on a watch glass before beginning the filtration process.

  11. Collect the crystals using vacuum filtration.

  12. Rinse the flask with about 5 mL of ice water and transfer the mixture to the funnel. Wash the crystals with 2 additional 1 mL portions of ice water.

  13. Dry the crystals in an oven for 10 minutes.

  14. Weigh the crude crystal, filter paper and watch glass.

  15. Warm ~15 mL of DI water (no higher than 70 °C)

  16. Add 5 mL of ethanol to a 50 mL beaker and transfer the crude crystals into the beaker.

  17. Gently warm (do not boil) the beaker until the crystals dissolve and immediately take off the heat.

  18. Add the 15 mL of warm water to the beaker and cool to room temperature.

CHM 2370 Rev 8/2019

  1. Cool the mixture in an ice-water bath for 10 minutes. If crystallization has not occurred, scratch the inside of the flask with a spatula to initiate crystallization. Also, chill 10-15 mL of DI water in a beaker.

  2. Weigh a piece of filter paper on a watch glass before beginning the filtration process.

  3. Vacuum filtration using a Büchner funnel.

  4. Rinse the flask with about 5 mL of ice water and transfer the mixture to the funnel. Wash the crystals with 2 additional 1 mL portions of ice water.

  5. Dry the crystals for 5 minutes by allowing air to drawn through them while they remain in the funnel.

  6. Transfer the product with the filter paper to a pre-weighed watch glass.

  7. Dry in your drawer until the next lab. You want a dry product in order to get a good IR.

  8. Next lab, weigh the watch glass, filter paper and pure product.

Calculations

  • Calculate the theoretical yield of aspirin


no data is required to find the THEORETICAL yield.

all you need is the procedure

Homework Answers

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Preparation of acetyl salicyclic acid (Aspirin) post-lab questions 1.) The FeCl3 test you performed on salicylic...
Preparation of acetyl salicyclic acid (Aspirin) post-lab questions 1.) The FeCl3 test you performed on salicylic acid, crude aspirin, and the purified aspirin gave different colors. Comment on the results you obtained in each of these tests in terms of colors and the functional groups present and what does that indicate about the purity of your purified aspirin? I got a dark purple color for saliclyc acid tube. "dark yellow" for crude aspirin tube, "llighter yellow" color for aspirin tube...
When using 3 grams of benzoin to oxidize to benzil, calculate the theoretical yield. Procedure: 2...
When using 3 grams of benzoin to oxidize to benzil, calculate the theoretical yield. Procedure: 2 boiling stones are added to a 400-mL beaker half-full of water, then placed on a hot plate to boil. 3 grams of benzoin and 7 mL of concentrated nitric acid are then added to a 125 mL Erlenmeyer flask and placed in the boiling water bath and left to boil until the evolution of nitrogen dioxide has ceased. Then, 50 mL of ice-cold water...
Experiment 1: Gravimetric Analysis with Calcium Chloride and Potassium Carbonate In this experiment, proper analytical experimental...
Experiment 1: Gravimetric Analysis with Calcium Chloride and Potassium Carbonate In this experiment, proper analytical experimental techniques will be utilized to perform a double displacement reaction. A solution will be prepared containing a known quantity of calcium chloride. Then, the mass of calcium present will be determined through a careful precipitation of calcium carbonate. You will also investigate the hygroscopic nature of calcium chloride through a comparison reaction. Materials: Scale250 mL Beaker50 mL BeakerStir rod4.0 g Calcium chloride, CaCl25.0 g...
Why is dinitration not a serious problem in this procedure? Nitration of Bromobenzene. (EAS) Procedure: mix...
Why is dinitration not a serious problem in this procedure? Nitration of Bromobenzene. (EAS) Procedure: mix 1ml concentrated sulfuric acid and 1mil concentrated nitric acid in a long-necked round bottom flask. Add a small stir bar, then place the flask in a 50mL beaker half-filled with water sitting on a magnetic stirrer. Using a connector, secure the flask to a ring stand and begin stirring the contents. Add .5ml bromobenzene dropwise while stirring the mixture. It is important to keep...
Add 7.0 mL of N,N-dimethylaniline and 50 mL of dichloromethane (CH2Cl2, DCM) to a 400- mL...
Add 7.0 mL of N,N-dimethylaniline and 50 mL of dichloromethane (CH2Cl2, DCM) to a 400- mL beaker. Place the beaker in an ice-water bath. Add a magnetic stir bar and thermometer. Clamp the thermometer in place. Turn on the stirring motor. Add 1.1 equivalents of a solution (~1 M) of bromine (Br2) in DCM (already prepared in the hood) with a plastic disposable pipet. If the temperature of the solution rises above 25 °C stop adding bromine solution. Allow the...
1. a) draw the structure of the product you would have isolated if you had used...
1. a) draw the structure of the product you would have isolated if you had used NaBD4 in D2O in this experiment, write a mechanism explaining the result. (b) give the product structure for the same reaction using NaBD4 in H2O. Assume that there is no hydrogen exchange between NaBD4 and the solvent. Not sure if this is relevant to the question but here is the procedure used: Dissolve 3.8g of vanillin in 12mL of ethanol in a small beaker...
Describe the role of the melting point depression phenomenon in this Solventless Aldol Experiment. the Eperiment:...
Describe the role of the melting point depression phenomenon in this Solventless Aldol Experiment. the Eperiment: Experimental Procedure: 1. in test tube, mix two solid reactants with spatula until an oil forms (melting point depression): In a small test tube, mix 0.25 g 3,4-dimethoxybenzaldehyde and 0.20 g 1-indanone. Crush the solids completely, using a glass rod or metal spatula. Caution: Avoid pressing hard on the bottom of the test tube. Continue stirring until a yellowish oil forms. 2. Add 50...
Questions are after the procedures. Procedure 1) For Trial 1, use a graduated cylinder to measure...
Questions are after the procedures. Procedure 1) For Trial 1, use a graduated cylinder to measure 5 mL of 1 M sodium sulfate (Na2SO4). Place the sodium sulfate in a beaker. Using a clean graduated cylinder, add 5 mL of 1 M calcium chloride (CaCl2) to the beaker. Stir to mix well. 2) Using two Büchner funnels as in the diagram below, set up a funnel system with a safety flask to protect the water system from contaminants. 3) Filter...
Calculate the percentage Yield of the preparation of Tris(thiourea)copper(I)chloridePreparation of Tris(Thiourea) Copper (I) Chloride Dissolve 5.0g...
Calculate the percentage Yield of the preparation of Tris(thiourea)copper(I)chloridePreparation of Tris(Thiourea) Copper (I) Chloride Dissolve 5.0g of Thiourea in 25 mL of hot Water, add 1.0g of Copper Turnings. In a fume hood, add 5 mL of concentrated HCl to this mixture. Heat this on a Steam bath while the Copper dissolves. Do not boil. Add Water if needed to maintain the liquid at a constant level. Filter the hot solution and allow to cool slowly. White opaque crystals will...
I need name of final compund and step by step equaions for the following experiment: Ethylenediamine...
I need name of final compund and step by step equaions for the following experiment: Ethylenediamine complexes of Nickel Procedure 1. Dissolve 1.3g NiCl2 6H2O in 1.5 mL of warm water. 2. With stirring, slowly add 5mL of 50% ethylenediamine solution 3. Cool in ice for 15 min., add 10mL ethanol(95%) and put back in the ice bath for 10min. 4.Filter, and then wash with two 10mL portions of ethanol and two 10mL portions of ether. 5. Air dry, weigh,...