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mead II. Short Synthesis. Beware of potential complications and be sure to avoid them. (10 pts each, 20 pts total) 1. Show how to carry out the following multi-step transformation using ANY additional carbon-carbon containing molecules and reagents necessary. Br CO₂H OH OH ४ 13-3/108 2. Starting with 3-(1-hydroxyethyl)benzaldehyde and propene as the only sources of carbon that end up in the product, show a synthesis of 3-(2-methylhept-2-en-3-yl)benzaldehyde. You may use any other reagents necessary. OH be H A

mead II. Short Synthesis. Beware of potential complications and be sure to avoid them. (10 pts each, 20 pts total) 1. Show how to carry out the following multi-step transformation using ANY additional carbon-carbon containing molecules and reagents necessary. Br CO₂H OH OH ४ 13-3/108 2. Starting with 3-(1-hydroxyethyl)benzaldehyde and propene as the only sources of carbon that end up in the product, show a synthesis of 3-(2-methylhept-2-en-3-yl)benzaldehyde. You may use any other reagents necessary. OH be H A

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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mead II. Short Synthesis. Beware of potential complications and be sure to avoid them. (10 pts each, 20 pts total) 1. Show how to carry out the following multi-step transformation using ANY additional carbon-carbon containing molecules and reagents necessary. Br CO₂H OH OH ४ 13-3/108 2. Starting with 3-(1-hydroxyethyl)benzaldehyde and propene as the only sources of carbon that end up in the product, show a synthesis of 3-(2-methylhept-2-en-3-yl)benzaldehyde. You may use any other reagents necessary. OH be H A
Transcribed Image Text:mead II. Short Synthesis. Beware of potential complications and be sure to avoid them. (10 pts each, 20 pts total) 1. Show how to carry out the following multi-step transformation using ANY additional carbon-carbon containing molecules and reagents necessary. Br CO₂H OH OH ४ 13-3/108 2. Starting with 3-(1-hydroxyethyl)benzaldehyde and propene as the only sources of carbon that end up in the product, show a synthesis of 3-(2-methylhept-2-en-3-yl)benzaldehyde. You may use any other reagents necessary. OH be H A
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