Dr. Frank's Magical Cure-all Cough Syrup contains three ingredients, shown below. Youseek to isolate these three ingredients to further quantify and analyze them, somethingthat can be achieved via liquid-liquid extraction. Propose a flow chart demonstrating howyou would separate each of the components into a distinct organic layer. This flowchartshould represent all of the chemicals required for the separation, and depict accuraterepresentations of the chemical species throughout the process.HH.НО

We have to make a flowchart to separate this three organic compound. The 2nd compound is converted…

Frank's Magical Cure-all Cough Syrup contains three ingredients, shown below. You ek to isolate these three ingredients to further quantify and analyze them, something at can be achieved via liquid-liquid extraction. Propose a flow chart demonstrating how u would separate each of the components into a distinct organic layer. This flowchart puld represent all of the chemicals required for the separation, and depict accurate presentations of the chemical species throughout the process. H HO

Frank's Magical Cure-all Cough Syrup contains three ingredients, shown below. You ek to isolate these three ingredients to further quantify and analyze them, something at can be achieved via liquid-liquid extraction. Propose a flow chart demonstrating how u would separate each of the components into a distinct organic layer. This flowchart puld represent all of the chemicals required for the separation, and depict accurate presentations of the chemical species throughout the process. H HO

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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Spectra E ZDO 180 160 140 120 100 BO ppm 60 S 40 20 10 7 S 2 1 0 ppm 4000 3000 2000 Wavenumbers, cm¹ 1500 1000 500 Structure: IR: 13C NMR: Number of types of C: Chemical shift(s) of signals: 'H NMR: Number of types of H: Chemical shift(s) of signals: • Integrations: • Multiplicity of peaks:
Please answer the question at the bottom, Thanks. LAB NOTES FOR PREPARATION OF BUTYL MAGNESIUM BROMIDEAND ITS SUBSEQUENT CONVERSION TO AN ALCOHOL To the reaction flask were added 2.5967 gram of magnesium turnings, about 20 mlof diglyme, and a solution of 13.5942 gram of butyl bromide in about 25 mldiglyme.The procedure as per the lab manual was initiated. After the required heating timewas completed the reaction mixture was allowed to cool to room temperature.Then a solution of 6.1123 gram of acetone in about 15 ml of diglyme was addeddropwise as per the lab manual.The rest of the lab manual procedure was completed, ultimately affording 2.5532gram of an oily, clear and slightly yellow liquid, presumed to be 2-methyl-2-hexanol. Boiling point as measured by distillation was 138 – 141 deg C.About 0.8 ml of the presumed 2-methyl-2-hexanol was placed in an NMR tube towhich was added 2 drops of TMS. The tube was capped, then inverted and righted20 times to thoroughly mix the product and…
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In this lab you used acid/base extraction to remove acidic impurities, how could basic impurities be removed through extraction? Imagine the two compounds below are both dissolved in ethyl acetate (a standard organic solvent for extractions), create a diagram/flow chart that outlines steps that could be taken to separate them through acid/base extraction and recover each compound in its neutral Be sure to track when each compound is in the organic or aqueous layer.
II. Draw the structure for the major Remember to transfer verbatim to your sheet of answels, 13. 1) ΗΝO3, H2SO, 2) H20, H30*, heat 3) NaOH, H20 14. 1) Br2, NaOH, H20 NH2 2) NaNO2, HCI, H20 (0-5°C) 3) CuBr 1) LIAIH, (excess) 15. CN 2) H20 (excess) CN 3) CI CI, pyridine 16. сно 1) НуNEt NABH;CN 2) PHCH,Br
Please answer the question at the bottom, Thanks. LAB NOTES FOR PREPARATION OF BUTYL MAGNESIUM BROMIDEAND ITS SUBSEQUENT CONVERSION TO AN ALCOHOL To the reaction flask were added 2.5967 gram of magnesium turnings, about 20 mlof diglyme, and a solution of 13.5942 gram of butyl bromide in about 25 mldiglyme.The procedure as per the lab manual was initiated. After the required heating timewas completed the reaction mixture was allowed to cool to room temperature.Then a solution of 6.1123 gram of acetone in about 15 ml of diglyme was addeddropwise as per the lab manual.The rest of the lab manual procedure was completed, ultimately affording 2.5532gram of an oily, clear and slightly yellow liquid, presumed to be 2-methyl-2-hexanol. Boiling point as measured by distillation was 138 – 141 deg C.About 0.8 ml of the presumed 2-methyl-2-hexanol was placed in an NMR tube towhich was added 2 drops of TMS. The tube was capped, then inverted and righted20 times to thoroughly mix the product and…
Comparison of specific functional group diagnostic peaks (C=O carboxylic acid, C-H, O-H carboxylic acid, O-H phenol, C=C) between Literature and Experimental spectra.
3 Draw a flow chart to shows the strategy for separation of three compounds: Phenanthrene and 4-Aminoacetophenone and 1,4-Dibromobenzen and dissolve mixture is Diethyl ether. add NaOH (1M) and (6M) to the aqueous layer and ether layer..
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Need must HANDWRITING THANKS. Dont copy paste. 2. Explain why we need to prepare a series of standard solutions with increasing concentrations during a UV-Vis analysis. How do you use it to determine the unknown?
Greetings, Can you please provide the solution to the attached question. Thank you
B. explain each step with words on how to get the structure. Step 1: Calculate the Index of Hydrogen Deficiency (IHD). Step 2: Use IR to determine obvious functional groups. Step 3: Use 1H-NMR to determine structural details. Step 4: Confirm the final structure using 13C-NMR.