3. » Synthesis. Complete 2 of the 4 syntheses below: 1 from a or b; 1 from c or d. Show a reaction, or series of reactions, you could use to synthesize each compound (in the best yield possible) given the organic reactions you know so far. You must use the starting material shown, but may use any inorganic reagent, common solvent, or temperature you need. Don't show mechanisms here. (You are welcome to use scratch paper to work out your ideas, though.) Make this... From this... HO, a HO, LOH b and HO Phenol HO and OH

3. » Synthesis. Complete 2 of the 4 syntheses below: 1 from a or b; 1 from c or d. Show a reaction, or series of reactions, you could use to synthesize each compound (in the best yield possible) given the organic reactions you know so far. You must use the starting material shown, but may use any inorganic reagent, common solvent, or temperature you need. Don't show mechanisms here. (You are welcome to use scratch paper to work out your ideas, though.) Make this... From this... HO, a HO, LOH b and HO Phenol HO and OH

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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3. ( series of reactions, you could use to synthesize each compound (in the best yield possible) given the organic reactions you know so far. You must use the starting material shown, but may use any inorganic reagent, common solvent, or temperature you need. Don't show mechanisms here. (You are welcome to use scratch paper to work out your ideas, though.) Synthesis. Complete 2 of the 3 syntheses below. Show a reaction, or Make this... From this... Benzene, and any organic compounds needed containing 5 or fewer carbons. a Benzene, and any inorganic compounds needed. .CI Benzene, and any alkene or alcohol needed containing 6 or fewer carbons.
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Citral is industrially synthesized from the enol ether of 3-methylprop-3-enal and 3,3- dimethylallylic alcohol (the starting material shown below). So right when you thought that all of that pericyclic stuff is just some esoteric nonsense, here they are, sigmatropic rearrangements in real life action. da a) Redraw the structures of the starting material and the intermediate, so that you have an easier time to indicate with curved arrows how the sigmatropic rearrangements (yes, there are two consecutive ones) are proceeding. b) Name the two sigmatropic rearrangements. heat heat الله citral H
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Provide the major organic product for each of the reactions below. If a specific stereochemistry will result, be sure to show that in your drawing. f) 1 of 2 H 1. B₂H6 2. NaOH, H₂O2, H₂O H₂, Pd/C
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