Please help me find the % yield and asnwer questions 1,2,3,4 de from acetanilide Synthesis of...
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...
can some one help me find a limiting reagent and percent tieldncalculation for acetanilide i started with 0.090 of acetanilide and after recryatallization i ended up with the product weigh 0.2346g. p bromoacetanilide. please explain and show each and every step Dispose of the filtrate from the Hirsch funnel tiltration 8P Al container for halogenated organic solvents rude proauct into a this mixture. Place all other filtrates into the R E Running the Reaction To a tared 5-mL conical vial...
Can someone tell me if a theoretical yield needs to be calculated for this experiment? And if so, how do you calculate it? please show all work. thank you. btw the aniline weighs 6.69g. Synthesis of Acetanilide Acetanilide is synthesized from aniline by a reaction known as acylation. Acylation is the addition of an acyl group to a compound. In this experiment, aniline (1 amine) is reacted with acetic anhydride (acylating agent) to form acetanilide (an amide). H-C-CH3 + CH...
Find %yield please the product obtained was 0.0870g In the hood, place 100 mu L of aniline in a tared 10 times 75 mm (small) test tube. Place the test cube in a small beaker or Erlenmeyer flask to avoid spillage. Stopper the cube with a cork. Now, using a Pasteur pipet, add (with swirling) 0.5 mL of water, followed by three drops of concentrated HCI. Add 10 mg of decolorizing charcoal (we use the pelletized form, called Nonrit^TM) to...
Make a purpose statement synthesis equation table of contents and theoretical yield for the synthesis of veratraldehyde oxime ( example given) NITRILE 1. SYNTHESIS oF VERATRALDEHYDE oxiME Review From previous lab procedures: suction filtration, recrystallization From organic chemistry text: sections 18.15, 18.16 Introduction oximes are usually prepared as derivatives of aldehydes and ketones, and they are used as a means of characterizing them and them. However, be reduced to amines or dehydrated to yield nitriles. Thus, they are also useful...
1 Calulate the percent yeild. Show work. explain the percent yield 2)Which stereoisomer of Dibromosuccinic acid(racemic melting point =170° C meso melting point = 290°C ) did you obtain? Draw it and showing mechanism to justify its transformation. PLEASE EXPLAIN 3) Explain the chemistry of the experiment. LAB /4-1-27 Preparation of Dibromosuccinic Acid Introduction: In this experiment, you will add bromine across the double bond of f mar determine the stereochemistry of your product via melting point. ou will then...
Please help me answer questions #1 through #12. Lab information and results are listed to the right side. Thank you! Paragraph . 1マーに 1 HTTL 2 | x' x, | so ea l E 1ヨ回ドもデ. | 2m 규亨ー过1K % Yield g aspirin obtained/ g aspirin calculated x 100 1. Mass of empty Erlenmeyer Flask,EF 2. Mass of EFsalicylic acid 3. Mass of EF+sslicylic acid + acetic anhydride 4. Mass of E 5. Calculate mass of salicylic acid used 8. Calculate...
I need it right now, please help me?? PROCEDURE PART I: DILUTING THE VINEGAR SOLUTION The vinegar solution must be diluted by a factor of 5 to be suitable for titration. 1. Obtain - 20 ml of the stock vinegar solution from the fume hood. 2. Using the 10-ml. pipet, pipet" 10 mL of the stock solution to a 50-ml volumetric flask. 3. Fill the volumetric flask to the calibration line with distilled water. Be sure not to go over...
Amount of Benzopincol recovered = 1.1g Amount of Benzopinacolone recovered = 0.5g Theoretical/Percent yield of Benzopinacol? Theoretical/Percent yield of benzopinacolone? Synthesis Module L Synthesis of Benzopinacolone In this reaction benzophenone goes through a proto of isopropyl alcohol. enone goes through a photochemical dimerization reduction to form benzopinacolone in the presence он он Ph + Acetone hv C- Phi Ph Ph-C- Ph-CSP + (CHỊ) CHOH. Ph Benzophenone Benzopinacol CH,COH, I Phác CầPh Ph Benzopinacolone Preparation of benzopinacol Add 2.0 gm benzophenone...
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,...