TLC is often used to monitor the progress of chemical reactions.
For example for the reaction A + B -----> C, how could you determine when the reaction is done? Explain thoroughly.
The reaction can be monitored easily using the TLC and can be understood from the image shown below:
The reactants can either be fully consumed or not completely consumed in the reaction as can be seen from the above image.
After spotting the reactants A, B and the reaction mixture or the product C in the respective positions in the baseline of the TLC plate, the TLC is run in eluents with increasing polarity (e.g. starting from pure hexane the TLC can be run with an increasing percentage of ethyl acetate or dichloromethane). Now each component of the reactants or products has each unique Rf value depending on the polarity of the eluent used. At a certain polarity, when the spots are significantly separated, from the Rf value one can check if any new spot has appeared or not in the C lane.
For this one has to run TLC from time to time. Now, two cases can happen-
(a) The A and B spot have completely disappeared, with the generation of a new spot C. Then the reaction is complete and should be quenched.
(b) The A and B spots are there along with another spot(s) in the C lane, and even after waiting for a long time or applying more drastic conditions, the spot intensities do not change i.e. the spots corresponding to A and B do not fade further. Then the reaction is finished and should be stopped.
TLC is often used to monitor the progress of chemical reactions. For example for the reaction...
4. TLC is a common method used to monitor reactions for completion. Consider the reaction below and draw the expected TLC plate for prior to the reaction, during the reaction, and after the reaction has completed. Only consider species A (1-hexene) and B (1-hexanol) on the TLC plates that you draw. 1. BH3-THF 2. NaOH, H202 VOH
4. TLC is a common method used to monitor reactions for completion. Consider the reaction below and draw the expected TLC plate for prior to the reaction, during the reaction, and after the reaction has completed. Only consider species A (1-hexene) and B (1-hexanol) on the TLC plates that you draw. 1. BH3-THF 2. NaOH, H2O2 HO B A
Explain how Thin Layer Chromatograpy (TLC) was used to monitor the progress of the second step of the diantilis synthesis ( the conversion of the benzyl alcohol into the diantilis product). Illustrate your answer by drawing representative TLC plates.
Wanting to monitor the reaction progress you decide to use normal phase thin-layer chromatography, but do not know what the best conditions are to use. If you had the standards for all potential products and your starting materials, outline how would you go about determining the best TLC conditions for monitoring the reaction progress. Provide drawings of an ideal TLC plate with the number of theoretical products you would expect and their relative positions. How do you know when the...
1.a IR spectroscopy and Thin Layer Chromatography (TLC) is very convenient in tracking reactions. Explain How you used both IR and TLC to track your reaction. Was your reaction complete when you did your initial TLC check? If so, how can you tell? 1.b Discuss how yield can be correlated to the efficacy of a reaction? Why are yields never 100%?
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 student monitored the reaction progress of the reduction of 4-Nitrobenzaldehyde to 4-Nitrobenzyl alcohol using TLC. 30% ethyl acetate in petroleum ether was used as the elution solvent. TLC plates available in the laboratory were coated with the common absorbent silica gel (SiO2.xH2O) which contains polar hydroxyl (OH-) groups. c. The crude product moves slower than the starting material with the mobile phase in the TLC plate. Briefly explain a possible reason for the observation based on the chemical structures...
Given the reaction below, consider how you could use IR spectroscopy to monitor the progress of the reaction. Select the correct instruction(s).
Describe how IR spectroscopy might be used to monitor the progress of the following reaction: H2Cr04 OH OH H20, H2S04 1-butanol butanoic acid
Explain how you used TLC analysis to identify each product obtained from the dihydroxylation reactions. Explain why 100% ethyl acetate was used to develop your TLC plate (and not 100% hexane or a mixture of hexane/ethyl acetate)?