Answer:
following alteration you can done in your procedure:-
1. Make the water ethanol solution 1:3 .
2. Increase the time of refluxing upyog hour because this reaction is too slow. If solvent evaporate during refluxing add more during the reaction.
By this you will definitely get the soap. If you don't get even by this alterations feel free to ask me.
What could I have done wrong in the saponification of the ester? I did not get soap 1.) Place .18 g of saturated triglyceride in a 5 mL short necked round bottom flask. 2.)Add 1.5 mL of a 50-50 wate...
5.0 ml of 2-methylcyclohexanol was placed in a 50 ml round bottom flask. Phosphoric acid (85%, 5 ml) was added cautiously, and the mixture swirled. Boiling stones were added to prevent bumping during heating. The mixture was heated to reflux temperature and refluxed for 15 minutes. The products were collected between 85-90 ˚C, in a small round bottom flask, cooled in ice water. Isolation Procedure The distillate was washed with 2 x 5 ml saturated sodium chloride solution in a...
Organic Chemistry Help! Questions and Exercises 1. In the course of reflux of the triglyceride in a sodium hydroxide solution you will notice a lot of foaming. Explain. What is left behind in the aqueous layer after filtration of the saponification product? The starting material and the product of the saponification reaction have similar melting points. How do you know you actually isolated a new product rather than just recovered the starting material? Give at least two different methods to...
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...
Thumbs up for good answer. Why does the liquid in the round bottom flask turn light pink?, please explain (This happened during/after step 2). This is the procedure and the experiment is called Synthesis of Artificial Flavorings by Fischer Esterification. Thank you! SAMPLE PROCEDURES: 1. Isoanvl acetate (banana) + H2O OH HO 1. Mix 6 mL of isoamyl alcohol (0.809 g/mL, 88.148 g/mol) and 10 ml ofglacial acetic acid (1.05 g/ml 60.05 g/mol) in a 100 mL round bottom flask....
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 with #3 please! SAFETY NOTES: Bromobenene and acetophenone are irritants. Wear gloves and avoid contact with skin, eyes, and clothing • MHC) is dritating to the skin avoid contact with the skin, eyes, and clothing Diethyl ether, usually referred to simply as "ether", is volatile and flammable. Keep a safe distance from hot electrical devices WASTE DISPOSAL *** A itrate is the liquid that passed through the Hirsch funnel, ending up in the bottom of the sidearm...
What is the SN2 reaction? How does Br attach to which carbon as a nucleophile and why? Difference between Unimolecular or Bimolecular? How NaBr and H2SO4 work in the reaction? Why Water/Sulfuric Acid/Brine/Sodium Hydroxide/Na2SO4 in Extraction? What does each layer have inside in each step of the separation? Please help. Due to corona, this is a theoretical lab and I am very confused. Chapter 16. The Sy2 Reaction: 1-Bromobutane Handout by Dr. Zhiyong Wang CH3CH2CH2CH, OH NaBr, H2SO4 ©Dr. Wang...
(4 pts) (4 pts) (4 pts) (1 pts) 5. Calculations 6. Conclusions 7. Post lab Questions 8. TA signature POST LAB QUESTIONS: 1. Why do we add methanol to the reaction if we see a purple ring? 2. What reaction is occurring with the methanol (show reaction)? Does this reactior affect your product? 3. Why do you get a precipitate when adding the HCl to make the solution acidic? Exp 8-5 Experiment 8: Preparation of Adipic Acid from Cyclohexene Oxidation...
CHEM 2001 Exp post lab Staple this to the post lab grade sheet... 5. Calculate the theoretical yield for this reaction using measurements from procedure. 6. If you obtained an actual yield of 0.57g. what is the yield? 7. What IR absorptions do you expect for the starting material (only in the functional group reg 4000cm to 1500cm)? 8. What IR absorptions do you expect for the product (only in the functional group region 4000cm 1500cm-')? to 9. If you...
What is the reaction product(s) of oleic acid & sodium methoxide? Show the structure(s). Part A: Acid Catalyzed Fischer Esterification of Free Fatty Acids Add 20 mL of canola oil and a magnetic stir bar to a 125-mL Erlenmeyer flask, and place the flask on a magnetic stirring plate. Add 2–3 mL of methanol and up to three drops of concentrated sulfuric acid Perform this step with caution, as this is a strong acid! Immerse a thermometer into the reaction...