Why would fluorene bind to dichloromethane more than fluorenone in TLC plates when fluorene is a non-polar molecule and fluorenone is a polar molecule?
Why would fluorene bind to dichloromethane more than fluorenone in TLC plates when fluorene is a...
Answer both please
Why does fluorenone travel more slowly than fluorene? Why does acetone speed up the rate at which fluorenone travels? (Make sure to include a picture of your TCL plate in your lab report)
use abbreviation structures!
2. a) Although fluorenone is more polar than fluorenol, more specific interactions between fluorenol and silica account for its slow migration in thin-layer chromatography. Below is a picture of the partial structure of silica. Using abbreviated structures for fluorenol and fluorenone, show the specific intermolecular interactions between these compounds and silica. Draw in extra silanol groups, as necessary. Use abbreviations such as R2CHOH and R2C-O. A good drawing will show at least two molecules of fluorenol [interacting...
When observing the TLC plates, were all the spots nice small circles? If no, provide and explanation as to why this might be the case. 3.
Why would it be unwise to use 100% ethyl acetate as the first mobile phase you test when determining the best mobile phase to separate the mixture of analgesics in Procedure? Why do polar compounds move slower up the silica TLC plates than nonpolar compounds? Why does increasing the polarity of the mobile phase increase the rate at which all compounds move up the plate?
can
you please answer all
1. When you run a TLC of the reaction in ethyl acetate : hexanes 1:1, the plate below is produced. Give a solvent system that would be expected to produce greater separation and a BRIEF (8 words) justification about your choice. (5 points) 7 6 5 4 3 b. Calculate the R for the bottom spot. (5 points) c. Which compound on the TLC plate is the most polar? (5 points) 2. Why is it...
Organic chemistry question
4. Benzoic acid is almost 12 times more soluble in dichloromethane than in water at room temperature (the distribution coefficient (K) is 11.7). a) Approximately how many grams of benzoic acid would be recovered in the organic layer if 10.0 g of benzoic acid dissolved in 100 mL of water was extracted with 100 mL of dichloromethane? Show calculations. b) Approximately how many grams of benzoic acid would be recovered if the water layer was extracted a...
TLC Analysis Of Egg Lipids Lab 1. The TLC plates were pre-baked at >120C. Why is this step necessary? 2. Below is the structure of your lipid staining dye, Naphthol Blue-Black. Explain which noncovalent interactions would be most important in allowing the dye to adhere to lipids (consider the chemical property of lipids as well as the dye). 3. You ran a solution of a fatty acid and a wax on a TLC plate using the exact conditions used in...
D Question 14 3.5 ts What is the line of solvent that moves up the TLC plate referred to as? O Solvent front O Capillary front Resolving factor Chromatographic boundary Question 15 3.5 pts Most organic compouds are colorless or white. A UV lamp assists in seeing your separation on TLC plates by: Making the organic sample spots glow and leaving the stationary phase dark Making the stationary phase glow, leaving dark spots where your sample is located Showing how...
1. When separating mixtures using TLC, why is it important to choose a solvent (mobile phase) that has a different polarity than the TLC plate (stationary phase)? 2. Why will some substances in a mixture travel farther up the TLC plate than others?
Question 26 1 pts When running a TLC, which of the following compounds would be more strongly absorbed onto the silica gel? O Compound A Compound B Compound B Compound A