I need to get the rf valuse from a made up value and draw a tlc plate of 30% ethyl actate and 70% peterloume ether Experimental Procedure.You will be using pre-prepared TLC plates and spotters in this experiment.In a small Erlenmeyer flask, dissolve 200 mg (1.30 mmol) of 4-nitrobenzaldehyde in 10ml of methanol.TLC will be used to monitor the progress of your experiment. Prepare a TLC plate sothat two spots will be eluted (Starting material – SM; Crude product 1 – CP1). Spot aTLC with your starting material (SM). The spot of the 4-nitrobenzaldehyde should bereadily visible by UV, since the compound absorbs very strongly in the UV region.Take the sodium borohydride out of the dessicator, quickly weigh out 70 mg of NaBH4,and put the sodium borohydride container back to the dessicator. Add the sodiumborohydride to the Erlenmeyer flask that contains the methanol solution of the 4-nitrobenzaldehyde, with stirring. In your laboratory notebook, record the time of additionof sodium borohydride to your reaction flask. Some of the sodium borohydride might notdissolve in the solution. These particles are an insoluble salt which is a product of thereaction.Now spot your second spot (of the reaction mixture that is stirring in your flasks) on theTLC plate (mark it CP1), and note the time in your lab notebook. While the reactionmixture is stirring, elute the TLC using 30% ethyl acetate in petroleum ether (30% ethylacetate; 70% petroleum ether). Remember to keep the elution solvent below the level ofthe TLC spots when you place the plate in the elution chamber.From this TLC, find out if there is any starting material (4-nitrobenzaldehyde) left in thereaction mixture. If there is none, stop stirring. Your reduction is complete. If there is stilla spot on the TLC due to the starting material, continue stirring for about five minutes,then take another TLC with one spot (mark it as CP2). If the reaction is still not complete,add some more sodium borohydride and continue stirring.After the reaction has been completed, add about 20 mL of methylene chloride(dichloromethane/ DCM), and pour the solution into a separatory funnel. Add 20 mL ofwater to the separatory funnel. Shake and let the aqueous and organic layers separate.Place the organic layer (which layer is that?) with your product in an Erlenmeyer flask.Repeat with another portion of methylene chloride. Combine the organic layers and add adrying agent. Gravity filter the solution into 100 mL pre-weighed round-bottom flask andwash the flask and drying agent with an additional 5mL of methylene chloride, alsofiltered into your round bottom flask. Evaporate the solvent on a steam bath in the hood(Erlenmeyer), or use the rotary evaporator (round bottom flask). Weigh the flask againand calculate the crude yield.(Be sure all solvent has been removed!) After the reaction has been completed, add about 20 mL of methylene chloride(dichloromethane/ DCM), and pour the solution into a separatory funnel. Add 20 mL ofwater to the separatory funnel. Shake and let the aqueous and organic layers separate.Place the organic layer (which layer is that?) with your product in an Erlenmeyer flask.Repeat with another portion of methylene chloride. Combine the organic layers and add adrying agent. Gravity filter the solution into 100 mL pre-weighed round-bottom flask andwash the flask and drying agent with an additional 5mL of methylene chloride, alsofiltered into your round bottom flask. Evaporate the solvent on a steam bath in the hood(Erlenmeyer), or use the rotary evaporator (round bottom flask). Weigh the flask againand calculate the crude yield.(Be sure all solvent has been removed!)Purification by recrystallization. Take a melting point of your crude product. Read thesection on recrystallization in your lab text before you come to class. Recrystallization isa technique for purification of a solid compound. In general, the compound (and anyimpurities) is dissolved in a minimal volume of hot solvent (or solvent mixture). This hotsolution is left to cool slowly to room temperature, and then placed in an ice bath. Thesolubility of compounds is less in colder solutions, so crystals of compound should formslowly from the saturated solution. (Since the impurity should be present in smallquantities, the impurity will stay in solution while the compound of interest iscrystallizing). If crystal formation is slow enough, the crystal should be pure compound.The purified compound is physically separated from solution by filtration. However, ifthis crystal formation is fast, impurities may be trapped in the rapidly forming lattice ofthe solid crystal. Therefore, it is important to be patient while performing arecrystallization.It may help you to see pictures of a movie of theprocess.Recrystallize the product from methylene chloride, and determine the weight percentagerecovery for this purification step once this purified solid has completely dried. If yourTLC of CP1 or CP2 contained multiple spots, take a TLC of the purified compound bydissolving a few crystals in methylene chloride and eluting with the same solvent asabove (30% ethyl acetate; 70% petroleum ether). Mark this purified product PP.

TLC can easily tell whether a reaction is complete or not. On a TLC plate, a polar compound takes…

Answered: I need to get the rf valuse from a made…

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...