- draw a flowchart showing the isolation of myristic acid from nutmeg
- Let’s say that you recovered 80% Trimyristin from 2 g of nutmeg you initially started with. If you competed the hydrolysis reaction to make myristic acid and glycerol, what would be your yield of myristic acid?
| Warm the sand bath first, and then turn it down to about 30°C |
| Weigh ground nutmeg on the filter paper |
| Transfer it to a round-bottom flask with a funnel and add 3mL of tert-butyl methyl ether and 3 boiling chips, connect the black distiller connector to the flask, and the distillation column. |
| Boil it for 10 minutes. After allowing the solids to settle, pipette the solution into a centrifuge tube. |
| Pipette it into a 25mL Erlenmeyer flask, through a pressure filtration device, Then put 2 mL of tert-butyl methyl ether into the round bottom flask, heat it again for five minutes, and repeat the same procedure. |
| Apply a very gentle breeze with air inside the fume hood so that the solution evaporated and left behind crude trimyristin. |
| Stand it to dry a few minutes, and recrystallize it with acetone. Let it cool in the ice bath for 15 minutes before collecting the crystals via vacuum filtration. Dry the crystals and place them on a piece of filter paper. Use some amount of the crystals for the hydrolysis. |
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Add trimyristin crystals to a round bottom flask with 2mL of 95% ethanol and 1 boiling chip. Heat it for 45 minutes. |
| After boiling, recrystallize the remaining trimyristin. After the hydrolysis, Let the solution cool, pour 8mL of distilled water into a 50mL Erlenmeyer and pour the solution into another flask. |
| In the fume hood, Measure 2mL of concentrated HCl dropwise, stir it with a glass stirring rod. A precipitate of Myristic acid will form. Cool the beaker for 10 minutes in the ice bath, collect the precipitate via vacuum filtration, and left them overnight to dry |
- draw a flowchart showing the isolation of myristic acid from nutmeg - Let’s say that...
Trimyristin is a fatty acid ester of myristic acid and glycerol. Draw the structure of the products of the base-catalyzed hydrolysis of trimyristin. Using this reaction, calculate a theoretical yield if you started with 1 g of trimyristin. Upload a picture showing all of your calculations. In our experiment we used 50mL of DCM and then refluxed and preformed a distillation to removed the excess DCM. We then used cool acetone to wash the crystals and then did vacuum filtration.
Reaction Workup and Purification For the reaction depicted below, draw a flowchart for the isolation of the ether product. Then explain why recrystallization would or would not be a good technique to purify the ester product this reaction. Assume the yield for this reaction is 92%. Follow up: What if the yield was 53%? Hints: Remember that recrystallization would happen after the work up/extraction! Think about what the yield could mean in terms of the product to reactant ratio at...
Post-Lab Questions 1. Formic acid (methanoic acid) is completely soluble in water. Draw the structures showing what formic acid is added to water. Name the product w the structures showing what happens when Formic acid HCOOH is completely soluble in y cecause of the hydrogen bonding. That is why HCOOH is complet 2. Formic acid can be neutralized with NaOH.Draw the structures for the neutralization reaction. Namen product 3. Hexanoic acid has an unpleasant odor. like the smell of goats....
1.0.980 g of acetylsalicylic acid was obtained from 1.00 g of salicylic acid by reaction with excess acetic anhydride. Calculate the percent yield of acetylsalicylic acid. 2. Two esters with the empirical formula C3H602 may be prepared. Write structural formulas for these esters and name them 3. How would you prepare the two esters in question 2? Draw a reaction for each. 1. Explain why you would or would not expect to observe a color change if FeClj were to...
Please show work completely, I would actually like to know how to do this for the future (a) If you started with 1.21 g of 3-nitrophthalic acid and had a 88% yield of 3-nitrophthalhydrazide, how many grams of 3-nitrophthalhydrazide were recovered? Be sure to show your work. (5 pts) (b) Based on the quantity of 3-nitrophthalhydrazide from above (a) how many grams of sodium dithionite would you need to perform the synthesis of luminol assuming you need 1.3 equivalents of...
6. Draw the conjugate acid of phenetidine and explain why it is highly soluble in water. Make sure to reference any relevant intermolecular forces as part of your answer. 6b. The solubility of dulcin in water is 1.21 g/L at room temperature. Assuming that you added a total of 82.5 mL of water between the reaction setup and the recrystallization process, how much dulcin (in mg) would remain in solution after recrystallization if you allowed the flask to cool to...
What is Zaitsev’s rule? Give the mechanism for the acid-catalyzed E1 reaction of 2-butanol. Give the mechanism for the base-catalyzed E2 reaction of 2-bromobutane. Draw all possible products. You expect three products from the elimination reaction 2-butanol. What are they? The E2 mechanism is a one-step mechanism. True or False? Explain. Which of these two alcohols would you expect to be more reactive under H3PO4/aqueous conditions? Why? Give the structure of the main product in both cases. 1-phenyl-1-propanol 1 -cyclohexyl-1-propanol...
question 4 & 5
Question 4 (2 points) if you accidently read the procedure wrong while doing the synthesis of aspirin and mixed Sg of salicylic acid with 2 mL of acetic anhydride (instead of correctly mixing 2g of salicylic acid with 5 mL of acetic anhydride), what would be the effect7(density of acetic anhydride = 1.082 g/mL) a Nothing, it would still work just fine Ob Reaction would work fine, but less product would form since acetic anhydride is...
I need to make a flowchart for this procedure but I am
not sure how to guide myself.
I was given this procedure which is for Suzuki-Cross
Coupling Reactiob: Synthesis of 4 - acetylbiphenyl, and I need to
make a flowchart. I need help with that.
Experimental Method 1. Place a stir bar in a 100 ml. RB flask filled with a lisen adapter and a reflux condenser, and then d-bromancelephence (1000 ml) photos acid (0.69 55 mmol) and 1-propanol...
1) Choose one molecule from the set and create an 8-step synthesis scheme using the chosen molecule as your starting material. You need to write the complete set of reagents and draw the product expected from each step. Reagents typically used together are considered one step, eg. 1) LAH 2) H.O should be considered as one step Your 8 steps must include at least one reaction from each of the chapters, aldehydes and ketones, carboxylic acid derivatives, alcohols. You can...