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
Part B: Base Catalyzed Transesterification of Triglycerides
Part C: Isolation of Product
Part D: Chromatographic and Spectral Data
What is the reaction product(s) of oleic acid & sodium methoxide? Show the structure(s). Part A:...
How can the NMP oxalate salt be converted back to NMP? Here is the procedure: PROCEDURES Part A: Synthesis of (±)-N,N-dimethyl-3-phenyl-3-(4-trifluoromethylphenoxy)propanamine To the 250-mL round-bottom flask (RBF) containing (±)-3-(dimethylamino)-1-phenylpropanol (product from Lab 6) and a magnetic stir bar, add 4 mL of 4-chlorobenzotrifluoride and 30 mL of dimethylacetamide (DMA). With stirring, add to this mixture 30 mL of 1.0 M potassium tert-butoxide (caustic alkali!) in tert-butyl alcohol using a syringe. Using a simple distillation apparatus, distill the mixture slowly, with...
Propose another way of synthesizing NMP from the amino ketone hydrochloride salt starting material you used. Part A: Synthesis of (t)-N,N-dimethyl-3-phenyl-3-(4- trifluoromethylphenoxy)propanamine 1. To the 250-mL round-bottom flask (RBF) containing (t)-3-(dimethylamino)-1-phenylpropanol (product from Lab 6) and a magnetic stir bar, add 4 mL of 4- chlorobenzotrifluoride and 30 mL of dimethylacetamide (DMA) 2. With stirring, add to this mixture 30 mL of 1.0 M potassium tert-butoxide (caustic alkali!) in tert-butyl alcohol using a syringe 3. Using a simple distillation apparatus,...
The alcohol could easily be converted to a tosylate, a good leaving group, and a conventional substitution reaction could have been performed instead of the nucleophilic aromatic substitution (NAS) reaction. Why was the NAS reaction the preferred method? (Hint : Look up the nucleophiles of both reactions on chemical manufacturing site.) Part A: Synthesis of (t)-N,N-dimethyl-3-phenyl-3-(4- trifluoromethylphenoxy)propanamine 1. To the 250-mL round-bottom flask (RBF) containing (t)-3-(dimethylamino)-1-phenylpropanol (product from Lab 6) and a magnetic stir bar, add 4 mL of 4-...
The alcohol could easily be converted to a tosylate, a good leaving group, and a conventional substitution reaction could have been performed instead of the nucleophilic aromatic substitution (NAS) reaction. Why was the NAS reaction the preferred method? (Hint : Look up the nucleophiles of both reactions on chemical manufacturing site.) Part A: Synthesis of (t)-N,N-dimethyl-3-phenyl-3-(4- trifluoromethylphenoxy)propanamine 1. To the 250-mL round-bottom flask (RBF) containing (t)-3-(dimethylamino)-1-phenylpropanol (product from Lab 6) and a magnetic stir bar, add 4 mL of 4-...
Predict the product(s) of the reactions for experiment B... 8. At reflux: At room temperature: TEMP Group B Substitution or Elimination As you have learned in lecture, substitution reactions and elimination reactions are competing reactions and the outcome of any reaction depends on several factors, most importantly tem- peratune, and the structure of the alkyl halide. This group will examine competition between substitution ánd elimimation reaction. Br NaOCH3 + (3-bromopropyl)benzene In a 25 mL round-bottom flask, add 2 mL of...
Why did you wash the ether solution with sodium bicarbonate? Write chemical equations for the reactions that took place. b. At which purification steps was the unreacted methanol removed in the reaction? Some of it may have been removed in more than one place. c. Three-Step Synthesis of Methyl Anisate (Step 3) 0 CHOH. Н.so, cat.) Wear gloves. Methanol is poisonous. Ether is an anesthetic, so don't breathe it. Sulfuric acid is a strong corrosive acid. Wash any you spill...
A Grignard reaction was performed using the following steps: Step 1: Addition of Grignard Reagent: Phenyl Magnesium Bromide a solution of phenyl magnesium bromide (2.7 mL of a 3.0 M solution in anhydrous diethyl ether) and 5 mL of anhydrous diethyl ether was dispensed into the round-bottom flask and stirred with a stir bar. Step 2: Addition Formation: Reaction with Benzophenone A solution of 0.72 g (mp = 48-49 degrees C) of benzophenone and 2.0 mL of anhydrous diethyl ether...
Post Lab Questions what is the purpose of glacial acetic acid in this reaction? (5 points) 2. How does KI-starch paper work? What is the source of the dark color 3. What is the purpose of adding saturated aqueous sodium bisult What reaction is taking place? Write out the bar my saturated aqueous sodium bisulfite to the reaction mixture? is taking place? Write out the balanced equation for this reaction. Why do you e kl-starch paper test after adding the...
SYNTHESIS OF T-PENTYL CHLORIDE LAB Provide a stoichiometry table for the reaction being performed in this lab. PROCEDURE Preparation oft-Pentyl Chloride In a 125-mL separatory funnel, place 10.0 mL of tert-pentyl alcohol (2-methyl-2- butanol, MW = 88.2, d = 0.805 g/mL) and 25 mL of concentrated hydrochloric acid (d 1.18 g/mL). Do not stopper the funnel. Gently swirl the mixture in the separa- tory funnel for about 1 minute. After this period of swirling, stopper the separatory funnel and carefully...
QUESTION: Show the mechanism of the reduction of 3-dimethylaminopropiophenone hydrochloride to form the alcohol? PROCEDURE: Add 2.00 g of 3-dimethylaminopropiophenone hydrochloride, 10 mL of distilled water and a magnetic stir bar to a 100 mL beaker, and stir to dissolve. This is the reaction beaker. Add (with stirring) sufficient 10% NaOH (about 5–6 mL) to bring the solution to pH >10. The free base will form and come out of solution as a milky oil. With continued stirring, add enough...