What is the Theoretical and Percent Yield in Cholesterol Nonanoate Synthesis?

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In summary, a student used 0.2543 g of cholesterol, 1.4 mL of pyridine, and 0.14 g of nonanoyl chloride in a reaction to form cholesterol nonanoate. The theoretically yield of cholesteryl nonanoate is 0.3465 g. At the end of the experiment, the student isolated 0.2254 g of cholesteryl nonanoate, resulting in a percent yield of 65%.
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~Sam~
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Homework Statement



A reaction of nonanoyl chloride with cholesterol to form cholesterol nonanoate, pyridine is also used in the reaction.

1.If a student starts with 0.2543 g of cholesterol, 1.4 mL of pyridine, and 0.14 g of nonanoyl chloride, what would be the theoretical yield of cholesteryl nonanoate?

2.At the end of the experiment, the student isolates 0.2254 g of cholesteryl nonanoate. What is the percent yield for this student’s synthesis?

Homework Equations



C9H17ClO + C27H46O -----(C5H5N) -----> C36H62O2 + C5H6NCl- (I believe that is the balance equation, any confirmation?

We are also given:
nonanoyl chloride M.W. = 176.7 g/mol
cholesterol M.W. = 386.6 g/mol
cholesteryl nonanoate M.W. = 527.2 g/mol


The Attempt at a Solution



I might have the solution but I'm not sure. First I believe that they all react with a ratio of 1mol, Using the balanced equation which says that ideally 1 mole of each of the three react together, it shows that C27H46O is the limiting substance as there it least of this. Therefore 1 mole cholesterol makes 1 mole of cholesteryl nonanoate, so 386g of cholesterol makes 526 g of cholesteryl nonanoate, so 0.2543g of cholersterol makes (526/386) x 0.2543 = 0.3465 g of cholesteryl nonanoate, which is the theoretical yield.

For 2) is it just % yield = (0.2254/theoretical yield) x 100
 
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  • #2
Approach seems to be OK, but I have just skimmed. I haven't checked numbers.

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  • #3
% = (0.2254/0.3465) x 100% = 65.1%

I would confirm that your calculations are correct. The balanced equation you have provided is correct and the ratio of 1 mole of each reactant is accurate. Your reasoning for cholesterol being the limiting substance is also correct.

For the first part, the theoretical yield would indeed be (0.2543 g cholesterol)(527.2 g cholesteryl nonanoate / 386.6 g cholesterol) = 0.3466 g cholesteryl nonanoate. So your calculation is very close to the theoretical yield.

For the second part, your calculation for percent yield is also correct. The student's actual yield is 0.2254 g, so the percent yield would be (0.2254 g / 0.3466 g) x 100% = 65.1%. This means that the student's experiment yielded 65.1% of the expected amount of cholesteryl nonanoate.

In addition, it would be helpful to mention the possible sources of error in this experiment. For example, the student may have lost some product during the isolation process or there could have been some side reactions that affected the yield. it is important to always consider and address potential sources of error in any experiment.
 

FAQ: What is the Theoretical and Percent Yield in Cholesterol Nonanoate Synthesis?

1. What is cholesterol nonanoate and why is it important to synthesize?

Cholesterol nonanoate is a chemical compound that is derived from cholesterol, a waxy substance found in our bodies that is essential for cell membrane structure and hormone production. Synthesizing cholesterol nonanoate allows scientists to study its properties and potential applications in fields such as medicine and materials science.

2. What is the process for synthesizing cholesterol nonanoate?

The synthesis of cholesterol nonanoate involves several steps, including the reaction of cholesterol with nonanoic acid in the presence of a catalyst, followed by purification and characterization of the resulting product. This process can be carried out in a laboratory setting using specialized equipment and techniques.

3. What are the potential uses of cholesterol nonanoate?

Cholesterol nonanoate has shown promise as a potential anti-cancer agent and as a building block for creating new materials with unique properties. It may also have applications in drug delivery and as a precursor for the synthesis of other compounds.

4. Are there any safety concerns associated with the synthesis of cholesterol nonanoate?

As with any chemical synthesis, there are potential safety hazards involved. It is important to follow proper safety protocols and handle all chemicals and equipment with care. It is also recommended to conduct the synthesis in a well-ventilated area and wear appropriate personal protective equipment.

5. What are the current challenges in synthesizing cholesterol nonanoate?

One of the main challenges in synthesizing cholesterol nonanoate is achieving high yields and purity of the final product. This requires precise control of reaction conditions and purification techniques. Additionally, finding more efficient and sustainable methods for synthesizing cholesterol nonanoate is an ongoing area of research.

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