ZI 2. C Your Task | X C Please Ans x E Untitled de X G differences X V Other Resc X tChemistry x M Inbox (1,6: x C Please Hel x 1HhCwVJEsyvdjZ7cD3mr6k-YnQAzMTRUIRSPVPaOAalo/edit ur student ID determines the mixture of compounds you're digit desired compound undesired impurity Но 1. OCH3 но HO-S HO-S-JOH -01-14 11-56.pdf 29°F Clou 直 0 +66 Extraction X M Inbox (1,6 x C Your Task X C Please Hel X C Please Ans X Untitled de X G differences X IV Other Resc x t Chemistry x ourses/1624739/assignments/9746808?module_item_id%3D22844972 Your task is to provide a procedure for purifying a desired organic compound by removing an undesired impurity, using the technique of extraction. To see what mixture you have been assigned, and whether you are working on regular scale (macroscale) or microscale, refer to this Google Doc2. The scale will influence how you go about performing the isolation of the desired compound. The scenario starts with a solution of the desired compound plus undesired impurity in the immiscible organic solvent of your choice. The solvent choice is not critical. However, if you take its density into consideration, your choice of solvent could make the procedure shorter. For reagents, you can assume that you have the following at your disposal: 5% aqueous HCI 5% aqueous NaOH saturated sodium bicarbonate • saturated sodium carbonate saturated aqueous sodium chloride sodium sulfate • extra immiscible organic solvent of your choice (e.g. if your initial mixture is dissolved in diethyl ether, extra diethyl ether will be available) Any laboratory glassware and equipment needed for the procedure (e.g. separatory funnel; rotary evaporator) would be available as well. Provide a written procedure for purifying the desired compound, starting from the impure organic solution and ending with the pure desired compound. The procedure should be detailed enough that an undergraduate student that has successfully completed the "live" CHEM325 lab could follow your procedure successfully and safely. Some guidance: They would need to be told what steps to perform, but it will be understood that they know how to perform the techniques involved. For example, "extract solution X with solution Y" doesn't require explaining how to grip a separatory funnel. They would need to be told whether the organic layer is the upper or the lower layer. • They also need to know what hazards are involved and what precautions to take. However, for this exercise, assume that the SDSS for all the compounds and reagents have already been reviewed with the student--you don't have to look up SDSS for this exercise. 2022-01-14 11-56.pdf a. +66 29°F Cloudy ^ 直 dy
ZI 2. C Your Task | X C Please Ans x E Untitled de X G differences X V Other Resc X tChemistry x M Inbox (1,6: x C Please Hel x 1HhCwVJEsyvdjZ7cD3mr6k-YnQAzMTRUIRSPVPaOAalo/edit ur student ID determines the mixture of compounds you're digit desired compound undesired impurity Но 1. OCH3 но HO-S HO-S-JOH -01-14 11-56.pdf 29°F Clou 直 0 +66 Extraction X M Inbox (1,6 x C Your Task X C Please Hel X C Please Ans X Untitled de X G differences X IV Other Resc x t Chemistry x ourses/1624739/assignments/9746808?module_item_id%3D22844972 Your task is to provide a procedure for purifying a desired organic compound by removing an undesired impurity, using the technique of extraction. To see what mixture you have been assigned, and whether you are working on regular scale (macroscale) or microscale, refer to this Google Doc2. The scale will influence how you go about performing the isolation of the desired compound. The scenario starts with a solution of the desired compound plus undesired impurity in the immiscible organic solvent of your choice. The solvent choice is not critical. However, if you take its density into consideration, your choice of solvent could make the procedure shorter. For reagents, you can assume that you have the following at your disposal: 5% aqueous HCI 5% aqueous NaOH saturated sodium bicarbonate • saturated sodium carbonate saturated aqueous sodium chloride sodium sulfate • extra immiscible organic solvent of your choice (e.g. if your initial mixture is dissolved in diethyl ether, extra diethyl ether will be available) Any laboratory glassware and equipment needed for the procedure (e.g. separatory funnel; rotary evaporator) would be available as well. Provide a written procedure for purifying the desired compound, starting from the impure organic solution and ending with the pure desired compound. The procedure should be detailed enough that an undergraduate student that has successfully completed the "live" CHEM325 lab could follow your procedure successfully and safely. Some guidance: They would need to be told what steps to perform, but it will be understood that they know how to perform the techniques involved. For example, "extract solution X with solution Y" doesn't require explaining how to grip a separatory funnel. They would need to be told whether the organic layer is the upper or the lower layer. • They also need to know what hazards are involved and what precautions to take. However, for this exercise, assume that the SDSS for all the compounds and reagents have already been reviewed with the student--you don't have to look up SDSS for this exercise. 2022-01-14 11-56.pdf a. +66 29°F Cloudy ^ 直 dy
Chemistry
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...
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