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Synthesis practice: Which alkene should be used with hydroboration to make the following alcohol. OH 1) BH3 2) H₂O₂ HOH

Synthesis practice: Which alkene should be used with hydroboration to make the following alcohol. OH 1) BH3 2) H₂O₂ HOH

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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**Synthesis Practice: Which Alkene Should Be Used with Hydroboration to Make the Following Alcohol?** In this exercise, you are tasked with determining the alkene that, when subjected to hydroboration, yields a specific alcohol product. **Reaction Conditions:** 1. \( \text{BH}_3 \) 2. \( \text{H}_2\text{O}_2/\text{OH}^- \) **Target Alcohol Structure:** The reaction yields an alcohol with a hydroxyl group (-OH) attached to a branched alkane chain, specifically placed on the second carbon. **Explanation:** - The target molecule is an alcohol with the hydroxyl group on a secondary carbon. - The hydroboration-oxidation process proceeds with anti-Markovnikov selectivity, meaning the OH group attaches to the less substituted carbon of the alkene. - Your task is to select the correct alkene that aligns with this mechanism to produce the specified alcohol as the primary product.
Transcribed Image Text:**Synthesis Practice: Which Alkene Should Be Used with Hydroboration to Make the Following Alcohol?** In this exercise, you are tasked with determining the alkene that, when subjected to hydroboration, yields a specific alcohol product. **Reaction Conditions:** 1. \( \text{BH}_3 \) 2. \( \text{H}_2\text{O}_2/\text{OH}^- \) **Target Alcohol Structure:** The reaction yields an alcohol with a hydroxyl group (-OH) attached to a branched alkane chain, specifically placed on the second carbon. **Explanation:** - The target molecule is an alcohol with the hydroxyl group on a secondary carbon. - The hydroboration-oxidation process proceeds with anti-Markovnikov selectivity, meaning the OH group attaches to the less substituted carbon of the alkene. - Your task is to select the correct alkene that aligns with this mechanism to produce the specified alcohol as the primary product.
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