Please don't provide handwritten solution ... This organic molecule is dissolved in a basic aqueous solution:HOOHA short time later sensitive infrared spectroscopy reveals the presence of a new C = O stretch absorption. That is, there must now be a new molecule presentwith at least one C = O bond.In the drawing area below, show the detailed mechanism that could convert the molecule above into the new molecule.Add/Remove step☑

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Answered: This organic molecule is dissolved in a…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter24: Catalytic Carbon-carbon Bond Formation

Section: Chapter Questions

Problem 24.8P

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This organic molecule is dissolved in a basic aqueous solution: OH OH A short time later sensitive infrared spectroscopy reveals the presence of a new C = O stretch absorption. That is, there must now be a new molecule present with at least one C = O bond. In the drawing area below, show the detailed mechanism that could convert the molecule above into the new molecule. 口 Add/Remove step X S
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1a) Provide the mechanism of the reaction below, catalyzed by triethylamine.The reaction should take you three mechanistic steps. Referring to the C=O group that already exists in the starting molecule: b) If this ketone were not present (for example, if it were just an H there instead), would the first step be faster or slower? Briefly explain. c) If this ketone were not present (for example, if it were just an H there instead), would the second step be faster or slower? Briefly explain. d) If 9.21 g of the starting reactant is used and 0.27 g of triethylamine are used, approximately how many reactions will each molecule of triethylamine catalyze? (hint: balance the equation)
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