Question

Explain why diethyl ether is a better choice for the extraction than ethanol. Extraction is triglyceride...

Explain why diethyl ether is a better choice for the extraction than ethanol. Extraction is triglyceride from nutmeg.

Homework Answers

Answer #1

Triglycerides have long hydrocarbon chains and are relatively nonpolar which makes them practically insoluble in polar solvents like water or alcohol. Thus using a relatively nonpolar solvent, the triglyceride can be easily extracted by the concept of "like dissolves like"(i.e., polar compounds are more likely to be soluble in polar liquids. Nonpolar compounds in nonpolar liquids). Diethyl ether is a relatively organic substance that can easily dissolve the triglyceride more than polar solvents like ethanol.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Explain why ethanol has a higher boiling point than diethyl ether. Draw to explain if needed.
Explain why ethanol has a higher boiling point than diethyl ether. Draw to explain if needed.
Which pair of solvents would make good extraction systems? diethyl ether and dichloromethane acetone and diethyl...
Which pair of solvents would make good extraction systems? diethyl ether and dichloromethane acetone and diethyl ether water and diethyl ether water and ethanol water and dichloromethane
If, by mistake, a chemist used 100% ethanol rather than diethyl ether as the reaction solvent,...
If, by mistake, a chemist used 100% ethanol rather than diethyl ether as the reaction solvent, would the Grignard synthesis still proceed as expected?
1.Explain why phenol is more acidic than cyclohexanol. 2.Explain why ethanol has a higher boiling point...
1.Explain why phenol is more acidic than cyclohexanol. 2.Explain why ethanol has a higher boiling point than diethyl ether.
EXTRACTION OF EUGENOL 1) You removed the diethyl ether from the Eugenol by means of a...
EXTRACTION OF EUGENOL 1) You removed the diethyl ether from the Eugenol by means of a simple distillation. What are two other methods by which the solvent could be removed?
Describe the process of liquid/liquid extraction using diethyl ether and water. Which layer is on top....
Describe the process of liquid/liquid extraction using diethyl ether and water. Which layer is on top. Is it considered organic or aqueous? explain in depth please
Diethyl ether is synthesized by heating ethanol with sulfuric acid at 130 degrees C to 140...
Diethyl ether is synthesized by heating ethanol with sulfuric acid at 130 degrees C to 140 degrees C. Only at higher temperatures does ethene become a significant product. Why does a strong acid such as H2SO4 yield the ether in this situation?
A. Explain why an Sn2 reaction between diethyl ether and sodium iodide is not favored but...
A. Explain why an Sn2 reaction between diethyl ether and sodium iodide is not favored but an sn2 reaction between diethyl ether and hydrogen iodide is more favorable. b. explain why the major product of either reaction is not ethene, even with heating
Grignard reaction questions? a. Ethanol is often present in solvent-grade diethyl ether. If this grade, rather...
Grignard reaction questions? a. Ethanol is often present in solvent-grade diethyl ether. If this grade, rather than anhydrous were used, what effect would the ethanol have on the formation of the Grignard reagent? b. Why is it necessary to acidify the mixture (addition of HCl) after the completion of Grignard reaction? c. Why is it necessary to clean and cut the magnesium ribbon into small pieces in the preparation of Grignard reagent? Thank you
LLE is often performed to separate an organic product from a reaction mixture. Diethyl ether is...
LLE is often performed to separate an organic product from a reaction mixture. Diethyl ether is used in this oxidation reaction. Why is more thanone extraction of the aqueous layer required? Explain on a microscopic level.