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1. A) Which of the following reactions below is correct and why? Br Br Br2 Br. Br 2HBR 1. В) Trifluoroacetic acid has been used in electrophilic addition reactions, and has been found to have the same mechanism of addition as a hydrogen halide: H. Propose a mechanism for the reaction above. 1.C) Keto-enol tautomeriation can be called a "proton jump" as the proton on the OH group "jumps" to the neighboring carbon. Draw the keto form of each of the following enols. LOH OH OH H3C, CH3

1. A) Which of the following reactions below is correct and why? Br Br Br2 Br. Br 2HBR 1. В) Trifluoroacetic acid has been used in electrophilic addition reactions, and has been found to have the same mechanism of addition as a hydrogen halide: H. Propose a mechanism for the reaction above. 1.C) Keto-enol tautomeriation can be called a "proton jump" as the proton on the OH group "jumps" to the neighboring carbon. Draw the keto form of each of the following enols. LOH OH OH H3C, CH3

Chemistry
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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1. A) Which of the following reactions below is correct and why? Br Br Br2 Br. Br 2HBR 1. В) Trifluoroacetic acid has been used in electrophilic addition reactions, and has been found to have the same mechanism of addition as a hydrogen halide: H. Propose a mechanism for the reaction above. 1.C) Keto-enol tautomeriation can be called a "proton jump" as the proton on the OH group "jumps" to the neighboring carbon. Draw the keto form of each of the following enols. LOH OH OH H3C, `N' CH3
Transcribed Image Text:1. A) Which of the following reactions below is correct and why? Br Br Br2 Br. Br 2HBR 1. В) Trifluoroacetic acid has been used in electrophilic addition reactions, and has been found to have the same mechanism of addition as a hydrogen halide: H. Propose a mechanism for the reaction above. 1.C) Keto-enol tautomeriation can be called a "proton jump" as the proton on the OH group "jumps" to the neighboring carbon. Draw the keto form of each of the following enols. LOH OH OH H3C, `N' CH3
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