Homework Answers
Correct answer is plate C. Since Rf value is constant for same compound irrespective of plate length. In plate A the Rf value of compound is nearly 0.7 which almost similar in plate C.
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6) Plate A, below, represents the TLC chromatogram of a compound run in hexanes. The same...
TLC Consider the following silica gel TLC plate of compounds A, B, and developed in hexanes:...
TLC Consider the following silica gel TLC plate of compounds A, B, and developed in hexanes: solvent front 0 D origin A B C 22. Determine the Ry values of compounds A, B, and Crun on a silica gel TLC plate using hexanes as the solvent. 23. Which compound, A, B, or C, is the most polar? 24. What would you expect to happen to the Ry values if you used acetone instead of hexanes as the eluting solvent? 25.TLC...
Post-Laboratory Questions Aspirin adnil tuleno Which compound turned out to be the most polar? The least polar? Do...
Post-Laboratory Questions Aspirin adnil tuleno Which compound turned out to be the most polar? The least polar? Do experimental results agree with your theoretical predictions? If not, why? 2. What would a chromatogram look like if a less polar developing solvent were used 3. Consider the following TLC plate of compounds A, B, and C developed in hexanes: solvent front starting line a) Determine the R values of compounds A, B, and C run on a silica gel TLC plate...
Please help 2. Consider the TLC plate shown below that was done on silica gel using...
Please help
2. Consider the TLC plate shown below that was done on silica gel using a solvent mixture of 4:1 hexane/EtoAc as the eluent. 4:1 Hexane:EtOAC marked solvent front Spot B Spot A A origin (a) Which of the two organic compounds labeled A and B is less polar? (b) Calculate the Rf value of compound B. (c) How would the following changes affect the Rf values of A and B? i. Change to a more polar solvent mixture...
can you please answer all 1. When you run a TLC of the reaction in ethyl...
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...
4. Consider the following silica gel TLC plac or compounds A, B, and hexines: developed in...
4. Consider the following silica gel TLC plac or compounds A, B, and hexines: developed in Fo-o- og a) Determine the Rr values of compounds A, B, and C run on a silica gel TLC plate using hexanes as the solvent b) Which compound, A, B, or C. is the most polar? values if you used acetone instead c) What would you expect to happen to the of hexanes as the eluting solvent? 5) Consider a sample that is a...
can you please answer all 1. When you run a TLC of the reaction in ethyl...
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) 9 10 8 7 LLLLLLL 6 5 4 001 2 3 b. Calculate the R for the bottom spot. (5 points) c. Which compound on the TLC plate is the most...
Possible Quiz Questions 1 What two methods of visualizing spots on a TLC plate will you...
Possible Quiz Questions 1 What two methods of visualizing spots on a TLC plate will you use in this Give two reasons why would you predict that the elution solvents (hexanes or acetate) would not be visible under UV visualization? week's lab? ethyl 2. Define R 3. Calculate the R of the spot on the following TLC plate. 4. Which compound in each pair is predicted to have the higher Ri? a. CH3CH2CH2CH2OH and CH3CH2CH2CH28r b. CH3CH2CH2CH2OH and CH3CH2CH2CH2CH2CH2CH3 c....
1) A student develops their TLC plate and places it under a UV light, but nothing...
1) A student develops their TLC plate and places it under a UV light, but nothing appears. What mistake might the student have made? a) Spotted the compound below the level of eluent b) Spotted the compound above the level of eluent c) Used a sample that was too concentrated d) Used too much sample 2)Thin layer chromatography, TLC, is commonly used to monitor reactions to completion. Using this technique, what would indicate to a student that the reaction is...
d. The following TLC plate was run with a mobile phase that consisted of 5% Ethyl...
d. The following TLC plate was run with a mobile phase that consisted of 5% Ethyl Acetate:95% Hexanes. Explain the result and describe what change to the mobile phase you would make to correct the issue. Solvent Fruct Speed Compound Line of One
6. Silica gel was used as the solid support for the TLC plate. Which of the...
6. Silica gel was used as the solid support for the TLC plate.
Which of the three compounds (A, B, or C) in the APPLIED MIXTURE is
the least polar? (See the figure attached.)
8. Which compound below will have the highest Rf on a TLC
plate? Explain your reasoning. (See figure attached.)
10. The following TLC plates have been spotted with two
different compounds and are about to be eluted. For each plate,
explain if it has been spotted...
TLC Consider the following silica gel TLC plate of compounds A, B, and developed in hexanes: solvent front 0 D origin A B C 22. Determine the Ry values of compounds A, B, and Crun on a silica gel TLC plate using hexanes as the solvent. 23. Which compound, A, B, or C, is the most polar? 24. What would you expect to happen to the Ry values if you used acetone instead of hexanes as the eluting solvent? 25.TLC...
Post-Laboratory Questions Aspirin adnil tuleno Which compound turned out to be the most polar? The least polar? Do experimental results agree with your theoretical predictions? If not, why? 2. What would a chromatogram look like if a less polar developing solvent were used 3. Consider the following TLC plate of compounds A, B, and C developed in hexanes: solvent front starting line a) Determine the R values of compounds A, B, and C run on a silica gel TLC plate...
Please help
2. Consider the TLC plate shown below that was done on silica gel using a solvent mixture of 4:1 hexane/EtoAc as the eluent. 4:1 Hexane:EtOAC marked solvent front Spot B Spot A A origin (a) Which of the two organic compounds labeled A and B is less polar? (b) Calculate the Rf value of compound B. (c) How would the following changes affect the Rf values of A and B? i. Change to a more polar solvent mixture...
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...
4. Consider the following silica gel TLC plac or compounds A, B, and hexines: developed in Fo-o- og a) Determine the Rr values of compounds A, B, and C run on a silica gel TLC plate using hexanes as the solvent b) Which compound, A, B, or C. is the most polar? values if you used acetone instead c) What would you expect to happen to the of hexanes as the eluting solvent? 5) Consider a sample that is a...
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) 9 10 8 7 LLLLLLL 6 5 4 001 2 3 b. Calculate the R for the bottom spot. (5 points) c. Which compound on the TLC plate is the most...
Possible Quiz Questions 1 What two methods of visualizing spots on a TLC plate will you use in this Give two reasons why would you predict that the elution solvents (hexanes or acetate) would not be visible under UV visualization? week's lab? ethyl 2. Define R 3. Calculate the R of the spot on the following TLC plate. 4. Which compound in each pair is predicted to have the higher Ri? a. CH3CH2CH2CH2OH and CH3CH2CH2CH28r b. CH3CH2CH2CH2OH and CH3CH2CH2CH2CH2CH2CH3 c....
d. The following TLC plate was run with a mobile phase that consisted of 5% Ethyl Acetate:95% Hexanes. Explain the result and describe what change to the mobile phase you would make to correct the issue. Solvent Fruct Speed Compound Line of One
6. Silica gel was used as the solid support for the TLC plate.
Which of the three compounds (A, B, or C) in the APPLIED MIXTURE is
the least polar? (See the figure attached.)
8. Which compound below will have the highest Rf on a TLC
plate? Explain your reasoning. (See figure attached.)
10. The following TLC plates have been spotted with two
different compounds and are about to be eluted. For each plate,
explain if it has been spotted...
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