Using TLC, unknown A was determined to have an Rf value of 0.87, unknown B was 0.64 and unknown C was 0.24. Which unknown is the most polar? How do you know?
In TLC, silica gel is polar so the polar compounds adhere to the silica gel runs slowly on the tlc plate giving a low rf value where as non polar compounds do not stick to the silica gel runs very fast on the tlc plate giving rise to high rf value.so the conclusion is polar compounds will have low rf value and non polar compounds will have high rf value.
unknown c is the most polar compound since it is having least rf value
unknown A is the most non polar and unknown B is moderately polar
Using TLC, unknown A was determined to have an Rf value of 0.87, unknown B was...
1. Calculate the Rf values for spots A and B on the TLC plate drawn below. Based on the Rf values which compound (A or B) is most likely to be more polar? a. Calculate Rf values for A and B b. Which compound A or B will most likely be polar? Why?
1. a) Why does biphenyl have a higher Rf value than either benzophenone or triphenylmethanol? Explain based on the structures and their effect on mobility in the TLC process. b) Which compound, benzophenone or triphenylmethanol has a higher Rf value? Explain, based on their structures, how you can predict this. c) You developed your TLC using a 10% mixture of diethyl ether in petroleum ether. Petroleum ether is a mixture of non-polar alkanes, so this TLC solvent is composed of...
Which compound should have the highest Rf value on a TLC plate? A acetanilide B nitroacetanilide C dinitroacetanilide
Which compound is likely to have the highest Rf value on silica gel TLC? Group of answer choices A) Benzoic Acid B) Dimethylaniline C) Benzophenone D) They will all have the same Rf value.
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)? 4. Determine the Rf value of the substances A, B, and Con the TLC shown. Show...
Which compound should have the highest Rf value on a TLC plate? (for Electrophilic Aromatic Substitution: Preparation of p-Nitroacetanilide experiment) A acetanilide B nitroacetanilide C dinitroacetanilide
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...
Ok, so what would happen if you are working with TLC and have a polar stationary phase (silica) and a mobile phase ( polar eluting solution) and you spot a nonpolar compound? Would the Rf values be greater than in a nonpolar mobile phase? I know in general if you are using TLC with polar silica and spot a nonpolar compound the nonpolar compound travels further (higher Rf values) because its chemical structure is different than the stationary phase compared...
3. TLC analysis of an unknown sample using pure ethyl acetate as a developing solvent gives a single spot with an Rf value of 0.08 1 points A. Explain why this result does not guarantee that the sample is a pure compound. B. Suggest two changes that could be made to the experiment to improve the analysis of the unknown sample. 2 points Change 1 Change 2
predict witch will have the highest rf value and witch will have the lowest out of naphthalene nonpolar butyric acid polar and phenyl acetate slightly polor when developed on a silica gel TLC plate using toluene as the mobile phase