Find %yield please the product obtained was 0.0870g In the hood, place 100 mu L of...
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...
I need help finding the theoretical yield (in grams) of triphenyl methanol product in this experiment. PLEASE SHOW WORK, I would like to learn the steps. below is pictures of the procedure with amounts of chemicals used 126 Experiment 10 EXPERIMENTAL PROCEDURE All glassware used in a Grignard reaction must be scrupulously dried, Dry the following glasstare in an af 110°C for at last 20 mini drying to Canadair 8 ml comical rial 5 ml con vial, air cond glass...
what is the percent yield of the lab procedure below? my final weight of the product is 0.0519 g sure of the proper disposal methodl, properly Check with your laboratory insructor if you are PROCEDURE Be sure to dry the 5-mL reaction vial in the oven for at least twenty minutes. Water is experiment. this Preparation of the Ylide 1. Place 0.480 g of benzyltriphenylphosphonium chloride in a dry, 5-mlL reaction vial containing a magnetic spin vane Add 2 mL...
1. What was the sodium sulfite used for the experiment below? 2. What material could still be in the ether layer of the experiment below? To a 3.0 mL conical vial containing a spin vane and equipped with an air condenser, add 20 uL of acetophenone and 700 uL of household bleach ( NaOCl, 5% available). Dispense both reagents in the hood! Stir the mixture at room temperature for thirty minutes. Add approximately 5.0 mg of sodium sulfite and stir...
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...
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 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...
What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this experiment? (Weight of triphenylmethanol: 0.060g) BACKGROUND AND THEORY The Grignard reaction was one of the first organometallic reactions discovered and is still one of the most useful synthetically. By reacting an organohalide (usually a bromide) with magnesium in ethereal solvent, carbon becomes a nucleophile. Grignard reagents are the starting points for the syntheses of many alkanes, primary, secondary, and tertiary alcohols, alkenes, and carboxylic...
i need help with post questions, thanks Product Isolation After stirring the reaction for 5 minutes and allowing the reaction mixture to cool (the reaction can be exothermic), remove the Claisen head from the conical vial. Slowly add 3 M HCl(aq) drop-wise. The solid may need to be broken up with a stirring rod or a pipet. Continue to add acid until the aqueous phase (bottom layer) tests positive with pH paper. Extractions can be done using the conical funnel...
What is the theoretical yield (in grams) and percent yield of your triphenylmethanol product in this experiment? Assume that you have collected 0.15g of Triphenylmethanol for the question. Reaction Set Up ---- ALL glassware NEEDS to be DRY!!! Anhydrous CaCl2 -Drying tube 53 mg Mg turnings Claisen adapter + 2 mL anhydrous ether + 260 ul bromobenzene Air condenser Stir until reaction amber. Heat slowly to reflux for 10 min. Cool the reaction in ice bath for 5 min. Use...
NaBH4(Sodium Borohydride) Reduction of Ketone (Organic Chemistry Lab) Questions 1. Explain the reaction mechanism and why each reagent was used. 2. Explain the need for 2 different drying agents 3. Use IR stretches and melting point determination to explain your results. 4. Report sources of error. Experiment Procedure Assemble the reaction apparatus as shown in Figure 14.2a, consisting of a 3.0 mL conical vial charged with 4-t- butylcyclohexanone (amount calculated in pre-lab) and methanol (100 μL). Attach the air condenser...