Post-lab Questions1. Create your own pH-dependent extraction experiment by separating two of any of thefollowing compounds in the table below. Do the following for both compounds.a. First, draw your chosen compounds in ChemDraw, including any non-bondingelectrons and non-zero formal charges.b. Circle and name any pH-sensitive functional groups.c.Choose an organic solvent that will dissolve both or your compounds and anaqueous solution (i.e. conc. aqueous NaOH, 5% aq. NaHCO3, or 3M HCl) thatwould successfully separate the two compounds you selected. Appendix C providesuseful information about common organic solvents.d. Write a procedure, similar to the one given in the experiment details, that aclassmate could follow to separate the two compounds. You may want to start bymaking a flow chart like the one shown in Appendix D to organize your thoughts.You should not turn in the flow chart if you choose to make one. Only turn in yourwritten procedure.O=p-anisic acidOHnaphthalenebenzophenone-N+ethyl-p-nitrobenzoateHOsesamolNH₂OHsalicylamide||_N+H₂N4-methyl-2-nitroanilineOHtrans-cinnamic acidbenzanilide

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Create your own pH-dependent extraction experiment by separating two of any of the following compounds in the table below. Do the following for both compounds.

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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