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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

Organic Chemistry: A Guided Inquiry
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter25: Enolate & Enol Nucleophiles
Section: Chapter Questions
Problem 5E
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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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