3. Three ways to make 2-ethoxyoctane from 2-octanol outlined below. Predict the product, A B, and C for each reaction, showing stereochemistry. Product A has an optical rotation of +15.6, what would you predict the rotation of B to be? For C? 1. Na 2. CH₂CH₂ OH entions 1. SOCI₂ B? 2. CH,CH,O A? 1. TsCl/pyr 2. CH;CH;O c?

3. Three ways to make 2-ethoxyoctane from 2-octanol outlined below. Predict the product, A B, and C for each reaction, showing stereochemistry. Product A has an optical rotation of +15.6, what would you predict the rotation of B to be? For C? 1. Na 2. CH₂CH₂ OH entions 1. SOCI₂ B? 2. CH,CH,O A? 1. TsCl/pyr 2. CH;CH;O c?

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter15: Radical Reactions

Section: Chapter Questions

Problem 14E

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