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1. (CF3CO0")2Hg, CH;OH 2. NABH4

1. (CF3CO0")2Hg, CH;OH 2. NABH4

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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Draw the structural formula for the major product as the following reaction

This image depicts a chemical reaction involving a cyclohexene derivative undergoing oxymercuration-demercuration. The process is a two-step reaction: 1. **Oxymercuration**: The reagent (CF₃COO⁻)₂Hg in methanol (CH₃OH) is used to add a methoxy group (OCH₃) across the double bond of the cyclohexene ring. 2. **Demercuration**: Sodium borohydride (NaBH₄) acts as a reducing agent to remove the mercury group, forming the final product with the methoxy addition. This type of reaction is typically used to achieve Markovnikov addition of alcohols to alkenes without the rearrangement that can occur in acidic conditions. It is valuable in organic synthesis for transforming alkenes into alkyl ethers.
Transcribed Image Text:This image depicts a chemical reaction involving a cyclohexene derivative undergoing oxymercuration-demercuration. The process is a two-step reaction: 1. **Oxymercuration**: The reagent (CF₃COO⁻)₂Hg in methanol (CH₃OH) is used to add a methoxy group (OCH₃) across the double bond of the cyclohexene ring. 2. **Demercuration**: Sodium borohydride (NaBH₄) acts as a reducing agent to remove the mercury group, forming the final product with the methoxy addition. This type of reaction is typically used to achieve Markovnikov addition of alcohols to alkenes without the rearrangement that can occur in acidic conditions. It is valuable in organic synthesis for transforming alkenes into alkyl ethers.
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