One student ran a TLC of an unknown compound on a silica gel plate and the distance from the starting line to the solvent front was 4 centimeters. the compound being analyzed had Rf of 0.25. Another student was analyzing another unknown compound by TLC on an identical plate but the distance from the starting line to the solvent front was 5 cm and the distance from the starting line to the compound was 1.25 cm. Are the students compounds the same? If not what additional experiments could be used to distinguish them?
The distance a compound moves in TLC is dependent on the stationary phase, mobile phase as well as the distance traveled by the solvent on the plate Since irrespective of the distance between the solvent front and the base, for the same mobile and stationary phases, the distance moved by a compound relative to the solvent front is constant, the parameter retention factor or Rf was established. It was given as:

So, the Rf of the unknown compound run by the second student will be:
Rf = 1.25/5 = 0.25,
which is also the Rf of the compound analyzed by the first student. Therefore, the compounds of both the students are identical according to TLC.
However, more than one molecule can have the same relative polarity and so show the same Rf for a particular mobile phase and stationary phase. So, to rule out any false-positives, structural analysis like NMR and IR spectra of the two compounds should be recorded and confirmed thus if they are indeed identical.
One student ran a TLC of an unknown compound on a silica gel plate and the...
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)
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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...
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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...
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...
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...
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...
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).
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. 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...
Thin Layer Chromatography (TLC) is a common technique that is routinely used in chemistry labs. It is simple, inexpensive, and very useful. Select the TRUE statement. More polar compounds travel faster on a TLC plate than less polar compounds. If compound A has a smaller Rf value than compound B, we can conclude that compound A is more polar than B. The stationary phase of a TLC silica gel plate is nonpolar. Rr is calculated as the distance traveled...