Question
Determine the theoretical yield and limiting reagent

Running the Reaction Add 0.100 g benzil and 0.30 mL 95% ethanol to a 3-mL conical vial. Place a spin vane in the vial and att
EXPERIMENT 32C Preparation of Benzilic Aciá Formation of Benzilic Acid ith swirling of the lask, add dropwise 0.50 mL of 1M h
Running the Reaction Add 0.100 g benzil and 0.30 mL 95% ethanol to a 3-mL conical vial. Place a spin vane in the vial and attach an air condenser. Heat the mixture with an aluminum block (90-100°C) while stirring until the benzil has dissolved (see inset in Tech- nique 6, Figure 6.1A). Using a 9-inch Pasteur pipette, add dropwise 0.25 mL of an aqueous potassium hydroxide solution' downward through the condenser into the vial. Gently boil the mixture (aluminum block about 110°C) while stirring for 15 minutes. The mixture will be blue-black. As the reaction proceeds, the color will turn to brown, and the solid should dissolve completely. Solid potassiunm benzilate may form during the reaction period. At the end of the heating period, remove the assembly from the aluminum block and allow it to cool for a few minutes Crystallization of Potassium Benzilate Detach the air condenser when the apparatus is cool enough to handle. Transfer the reaction mixture, which may contain some solid, with a Pasteur pipette into a 10-mL beaker. Allow the mixture to cool to room temperature and then cool in an ice-water bath for about 15 minutes until crystallization is complete. It may be necessary to scratch the inside of the beaker with a glass stirring rod to induce crys- tallization. Crystallization is complete when virtually the entire mixture has solid- ified. Collect the crystals on a Hirsch funnel by vacuum filtration and wash the crystals thoroughly with three 1-mL portions of ice-cold 95% ethanol. The solvent should remove most of the color from the crystals. Transfer the solid, which is mainly potassium benzilate, to a 10-mL Erlenmeyer flask containing 3 mL of hot (70°C) water. Stir the mixture until all solid has dis solved or until it appears that the remaining solid will not dissolve. Any remaining solid will likely form a fine suspension. If solid does remain in the flask, filter the mixture in the following manner. Place about 0.5 g of Celite (Filter Aid) in a beaker with about 5 mL of water. Stir the mixture vigorously and then pour the contents into a Hirsch funnel (with filter paper) or a small Büchner funnel while applying a gentle vacuum, as in a vacuum filtration (Technique 8, Section 8.3, and Figure 8.5) Be careful not to let the Celite dry completely. This procedure will cause a thin layer of Celite to be deposited on the filter paper. Discard the water that passes through this filter. Pass the mixture containing potassium benzilate through this filter, using gentle suction. The filtrate should be clear. Transfer the filtrate to a 10-mL Erlern meyer flask. If no solid remains in the flask, the filtration step may be omitted. In either case, proceed to the next step
EXPERIMENT 32C Preparation of Benzilic Aciá Formation of Benzilic Acid ith swirling of the lask, add dropwise 0.50 mL of 1M hydrochloric acid to the ion of potassium benzilate. As the solution becomes acidic, solid benzilic acid H should be about 2; if it is higher than this, add a will begin to precipitate. The p few more drops of acid and check the pH again. Allow the mixture to cool to room temperature and then complete the cooling in an ice bath. Collect the benzilic acid by vacuum filtration using a Hirsch funnel. Wash the crystals with 3-4 mL of ice- cold water to remove potassium chloride salt that sometimes coprecipitates with benzilic acid during the neutralization with hydrochloric acid. Remove the wash water by drawing air through the filter. Dry the product thoroughly by allowing it to stand until the next laboratory period. Melting Point and Crystallization of Benzilic Acid Weigh the dry benzilic acid and determine the percentage yield. Determine the melt- ing point of the dry product. Pure benzilic acid melts at 150°C. If necessary, crystal- lize the product from hot water using a Craig tube (Technique 11, Section 11.4, and Figure 11.6). If some impurities remain undissolved, filter the mixture using the fol- lowing procedure. It will be necessary to keep the mixture hot during this filtration step. Transfer the hot mixture to a test tube with a Pasteur pipette. Clean the Craig tube and filter the mixture by transferring it back to the Craig tube with a filter-tip pipette. Cool the solution and induce crystallization, if necessary. Allow the mixtur to stand at room temperature until crystallization is complete (about 15 minutes Cool the mixture in an ice bath and collect the crystals by centrifugation. Determin the melting point of the crystallized product after it is thoroughly dry он о 30 C-C-OH 25 20 15
0 0
Add a comment Improve this question Transcribed image text
Answer #1


Date olction0R Reacion for Benzilic aid Benzil holAgueous PotasSjum hydroxide Relux Intesmediadte EL OK rochIonc teumediate aTheore tial yield 一 -Theoretical yield is the, calculati not amount of the benzilcadd.Produted-dring the radion. As annou ot

Add a comment
Know the answer?
Add Answer to:
Running the Reaction Add 0.100 g benzil and 0.30 mL 95% ethanol to a 3-mL conical vial. Place a s...
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. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Place 3.0 g of salicylic acid in a 125-ml Erlenmeyer flask. Carefully add, stirring constantly, 6...

    Place 3.0 g of salicylic acid in a 125-ml Erlenmeyer flask. Carefully add, stirring constantly, 6 mL of acetic anhydride, followed by 10 drops of concentrated sulfuric acid. Swirl the contents of the flask so that the reactants are thoroughly mixed. Stopper the flask with a one- hole cork fitted with an inverted Pasteur pipet to prevent condensation of water in the reaction flask during heating on the steam bath. Heat the flask in a boiling-water or steam bath for...

  • QUESTION: Write a flow scheme for the work-up. THE WORK UP:

    QUESTION: Write a flow scheme for the work-up. THE WORK UP: C. Work-up (save all layers) and Isolation of Product MgBrCl Benzoic acid Transfer the mixture into a test tube. Rinse the beaker with about 3 mL of regular (not anhydrous) diethyl ether and pour the washings into the test tube. There should be two distinct layers in the test tube Remove the aqueous layer (to be discarded) and shake the ether layer with about 2 mL of 3 M...

  • 1.) What side reactions occur during the following steps. 2.) How can the IR spectrum be...

    1.) What side reactions occur during the following steps. 2.) How can the IR spectrum be used to show that there is not starting material left and the products are ketones? 3.) Describe the major differences and similarities between the IR spectra of benzoin and benzil. Compare your IR spectrum with those of benzoin and benzil. Copper-Catalyzed Oxidation of Benzoin 1. Add a stir bar and 1.5 mL of glacial acetic acid, 0.250 g of NH4NO3 and 0.500 g of...

  • used. Experimental . Place 2.0 g of salicylic acid in a 125-mL conical flask. 2. Add...

    used. Experimental . Place 2.0 g of salicylic acid in a 125-mL conical flask. 2. Add 4.0 ml (d = 1.08 g/mL; 4.3 g) of acetic anhydride and 6-8 drops of 85% phosphoric acid. 3. Swirl the flask to mix all reagents, and place it in a 70°C water bath. Heat for about 10 minutes. 4. Remove the flask from the water bath and add 2 mL of cold water drop- wise, swirling the flask after each addition, 5. Add...

  • Write out your separation scheme for this experiment. 1. Heat 75 mL of water to 90...

    Write out your separation scheme for this experiment. 1. Heat 75 mL of water to 90 °C in a 250-mL beaker. 2. While the water is being heated, place 250 mg of salicylic acid, 1 drop of 85% phosphoric acid and 0.5 mL of acetic anhydride in a test tube. Add a boiling chip to the mixture and gently shake it in order to mix the reactants. 3. Heat the tube in the beaker of water at 85 - 90...

  • Draw a pathway for the reaction of phenylboronic acid with 4-iodophenol to obtain 4-phenylphenol in the...

    Draw a pathway for the reaction of phenylboronic acid with 4-iodophenol to obtain 4-phenylphenol in the form of a catalytic cycle. EXPLAIN and STATE all complexes formed in EACH STEP by their electron counts (count how many e- are there, e.g. 18 e- or 16 e- etc.), formal oxidation states and all the reactions with mechanistic labels (i.e. oxidative addition, reductive elimination, etc.) (note the amount of base used). Be sure to EXPLAIN the catalytic cycle as to what happens...

  • Can you explain how to find what is the theoretical yield, and the desired percent yield...

    Can you explain how to find what is the theoretical yield, and the desired percent yield of ethyl 4-nitrobenzoate? 1. Synthesis of ethyl 4-nitrobenzoate a) In a 50-ml round-bottom flask, weigh out 4-nitrobenzoic acid (0.85 g, 0.005 mol). Add to this 8 ml of absolute ethanol. Add boiling stones, and then bring this solution to the Lab Technologist. WATER OUT b) The Lab Technologist will deliver 1.2 ml of concentrated sulfuric acid to the mixture from the automatic pipette. [CAUTION,...

  • PROCEDURE 1. Place a reaction tube into a 5-mL Erienmeyer and tare. Add between 0.275- 0.300g...

    PROCEDURE 1. Place a reaction tube into a 5-mL Erienmeyer and tare. Add between 0.275- 0.300g of salicylic acid. Record on the data sheet. 2. Transfer the reaction tube and 5-ml Erienmeyer to the hood. Add a boiling chip, 2 drops of 85% phosphoric acid, and about 0.70 mL of acetic anhydride to the reaction tube. Mix well. 3. Place a 50-ml beaker containing about 20-mls of water on a hot plate or in the sand bath. Allow the water...

  • What is the mechanism (with curved arrows) for this reaction? 1. Add about 1.0 g (measured accurately) of acetophenone t...

    What is the mechanism (with curved arrows) for this reaction? 1. Add about 1.0 g (measured accurately) of acetophenone to 40 mL of the bleach solution (5% NaCl in water - this reactant should be included in your table of reagents!) in a 100 mL round bottom flask equipped with a magnetic stirrer. Clamp the flask in the fume hood above a stir plate. 2. After the initial reaction has subsided, boil the reaction mixture gently for 5 - 10...

  • Bromination of Acetanilide In a 25-mL Erlenmeyer flask, dissolve 0.68 g of acetanilide in approximately 4...

    Bromination of Acetanilide In a 25-mL Erlenmeyer flask, dissolve 0.68 g of acetanilide in approximately 4 mL glacial acetic acid. Record the exact amount of the limiting reactant that you used. Add a stir bar followed by 1.6 g pyridinium tribromide. Heat the mixture to ~60°C in a warm water bath for 10 minutes. After the 10 minutes, add 15 mL water and approximately 2 mL saturated sodium bisulfite solution to remove excess bromine, which shows by the disappearance of...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT