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Question 26 1 pts When running a TLC, which of the following compounds would be more...
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...
Which of the following compounds would you expect to have the lowest Rf value on a...
Which of the following compounds would you expect to have the lowest Rf value on a silica gel TLC plate developed with dichloromethane? O A. Naphthalene O B. Phenyl acetate OC Butyric acid QUESTION 3 Which of the following compounds would you expect to have the highest Rf value on a silica gel TLC plate developed with dichloromethane? O A 2-octanone O B. Acetic acid C. 1-butanol OD. decane E. acetaldehyde
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...
Question 9 1 pts Considering the silica gel TLC plate shown, which compound is the most...
Question 9 1 pts Considering the silica gel TLC plate shown, which compound is the most polar (the solvent front is at 4.0 cm)? Spot Distance traveled (cm) A 0.50 В 2.0 IC 3.0 D 1.0 O Compound B (spot B) Compound A (spot A) O Compound D (spot D) O Compound C (spot C)
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...
1. which of the following are not absorbent for TLC? a. magnesium silicate b. polyamides c....
1. which of the following are not absorbent for TLC? a. magnesium silicate b. polyamides c. silica gel-F ( fluorescing indicator added) d. starch e. alumina f. none of the above 2. select the best answer from the statements below about thin layer chromatography A. in normal phase thin layer chromatography the stationary phase is polar silica gel b. in normal phase thin layer chromatography the mobile phase is an organic solvent or a mixture of organic solvents Which is...
kindly answer the following thank you! 3. Since the surface of the silica gel on a...
kindly answer the following thank you!
3. Since the surface of the silica gel on a silica gel TLC plate is covered in SI-O-H groups, organic molecules that can hydrogen bond will be much more attracted to the silica gel surface. Given that which of the following compounds would have the lowest Rf value if each of these was analyzed using a slica gel TLC plate and dichloromethane as a solvent? OH 4. Determine the Rf values for the two...
1. When 2-propanol was used as the developing solvent, two substances moved with the solvent front...
1. When 2-propanol was used as the developing solvent, two substances moved with the solvent front (Rf= 1) during TLC analysis on a silica gel plate. Can you conclude that they are identical? If not, what additional experiment(s) would you perform? 2. The Rf value of compound A is 0.34 when a TLC plate is developed in hexane and 0.44 when the plate is developed in diethyl ether. Compound B has an Rf value of 0.42 in hexane and 0.60...
3) Consider the compounds trans-4-tert-butylcyclohexanol (1) and 4-tert-butylcyclohexanone (2) below. Using silica gel...
3) Consider the compounds trans-4-tert-butylcyclohexanol (1) and 4-tert-butylcyclohexanone (2) below. Using silica gel TLC plates, which of the two compounds will have the higher R value when dichloromethane is the developing solvent? Why? (5 pts).
1. A mixture containing Compound X and Compound Y is analyzed using silica gel TLC. a....
1. A mixture containing Compound X and Compound Y is analyzed using silica gel TLC. a. If Compound X has an Rf value of 0.7 and Compound Y has an Rvalue of 0.3, which compound is more polar? Explain. b. The solvent traveled 50 mm. How far did Compound Y travel? 2. Why isn't it reasonable for an R. value to be greater than 1? 3. How many spots would you expect to see if you conducted a TLC separation...
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...
Which of the following compounds would you expect to have the lowest Rf value on a silica gel TLC plate developed with dichloromethane? O A. Naphthalene O B. Phenyl acetate OC Butyric acid QUESTION 3 Which of the following compounds would you expect to have the highest Rf value on a silica gel TLC plate developed with dichloromethane? O A 2-octanone O B. Acetic acid C. 1-butanol OD. decane E. acetaldehyde
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...
Question 9 1 pts Considering the silica gel TLC plate shown, which compound is the most polar (the solvent front is at 4.0 cm)? Spot Distance traveled (cm) A 0.50 В 2.0 IC 3.0 D 1.0 O Compound B (spot B) Compound A (spot A) O Compound D (spot D) O Compound C (spot C)
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...
kindly answer the following thank you!
3. Since the surface of the silica gel on a silica gel TLC plate is covered in SI-O-H groups, organic molecules that can hydrogen bond will be much more attracted to the silica gel surface. Given that which of the following compounds would have the lowest Rf value if each of these was analyzed using a slica gel TLC plate and dichloromethane as a solvent? OH 4. Determine the Rf values for the two...
1. When 2-propanol was used as the developing solvent, two substances moved with the solvent front (Rf= 1) during TLC analysis on a silica gel plate. Can you conclude that they are identical? If not, what additional experiment(s) would you perform? 2. The Rf value of compound A is 0.34 when a TLC plate is developed in hexane and 0.44 when the plate is developed in diethyl ether. Compound B has an Rf value of 0.42 in hexane and 0.60...
3) Consider the compounds trans-4-tert-butylcyclohexanol (1) and 4-tert-butylcyclohexanone (2) below. Using silica gel TLC plates, which of the two compounds will have the higher R value when dichloromethane is the developing solvent? Why? (5 pts).
1. A mixture containing Compound X and Compound Y is analyzed using silica gel TLC. a. If Compound X has an Rf value of 0.7 and Compound Y has an Rvalue of 0.3, which compound is more polar? Explain. b. The solvent traveled 50 mm. How far did Compound Y travel? 2. Why isn't it reasonable for an R. value to be greater than 1? 3. How many spots would you expect to see if you conducted a TLC separation...
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