Determine the Rf value of the substances A, B, and C on the TLC shown. Show your calculation!
What will happen if the applied spot is lower than the level of the developing liquid?
What will be the result of applying too much compound on a TLC plate?
What is the reason that the mobile phase travels up the silica gel plate (TLC plate)?
Determine the Rf value of the substances A, B, and C on the TLC shown. Show...
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 experiments(s) would you perform?
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...
2) During silica gel TLC analysis, when 2-propanol was used as a developing solvent, two substances moved with the solvent front (Rf = 1.0). Can you conclude that the substances are identical? If not, what additional experiment(s) would you perform? (5 pts).
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...
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...
A silica gel TLC plate was spotted using compounds A-D and developed in hexane. Spot “B” traveled a distance of 2.0 cm from the solvent front at 4.0 cm, which of the following is a correct way to calculate its Rf value? Spot Distance traveled (cm) A 0.50 B 2.0 C 3.0 D 1.0 Spot B Rfis 4.0 cm/0.20 cm = 2.0 Spot B Rf is 4.0 cm/(4*2.0 cm) = 0.50 Spot B Rfis 2.0 cm/4.0 cm = 0.50 Spot...
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)
Question 18 (3 points) What is the Rf value for the TLC spot shown? The scale is shown next to the TLC, where each marking is one unit apart. solvent front IIIIIIIIIIIIIII O origin 0 0.50 O 0.45 0.53 0.40
1) Calculate the Rf value of a spot that travels 5.7 cm, with a solvent front that travels 13 cm. 2) A student spots an unknown sample on a TLC plate and develops it in pentane solvent. Only one spot, for which the Rf value is 0.05, is observed. Is the unknown material a pure compound? What can be done to verify the purity of the sample using thin-layer chromatography? 3) You try to synthesize n-hexyl bromide as a product...
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...