7. Predict the product and draw the 2-step mechanism. 1. ROH attacks ZnCl2, giving the O-atom a (+) charge andZn a (-). The ZnCl, does not lose a CI- ion, it's simply attached to the OH group. 2. Then a CH ion attacksand kicks off the better leaving group (Sn2).ZnCl2HO

Answered: 7. Predict the product and draw the…

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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In the reaction below, the highlighted part is.... Br CN CN A) A starting material B) A product C) A nucleophile D) An electrophile E) A leaving group
4. Draw the final major product(s) for each multistep synthesis reaction. H3O* OMe H3PO4 Jones Et,NH reagent H30* PBR3 KOC(CH3)3 1. O3 NABH3CN HO- 2. DMS NH3, H3O* Br KOC(CH3)3 1. ВНз PCC H3O* 2. H2О2, ОН CH2CI2
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This question has multiple parts. Work all the parts to get the most points. The Stork reaction is a condensation reaction between an enamine donor and an a,ß-unsaturated carbonyl acceptor. The overall reaction consists of a three-step sequence of 1. formation of an enamine from a ketone, 2. Michael addition to an a,ß-unsaturated carbonyl compound, and 3. hydrolysis of the enamine in dilute acid to regenerate the ketone. Consider the Stork reaction between cyclohexanone and propenal. 1 Draw the structure of the product of the enamine formed between cyclohexanone and pyrrolidine. TAYY { n [F ? ChemDoodle Previous Next

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7. Predict the product and draw the 2-step mechanism. 1. ROH attacks ZnCl2, giving the O-atom a (+) charge and Zn a (-). The ZnCl, does not lose a CI- ion, it's simply attached to the OH group. 2. Then a CH ion attacks and kicks off the better leaving group (Sn2). ZnCl2 HO