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Me Br2, hv Me Me H-Br HO, (2 equiv) HO, SOCI, base [assume SN2] OH H

Me Br2, hv Me Me H-Br HO, (2 equiv) HO, SOCI, base [assume SN2] OH H

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 main product you expect from each reaction below. Pay attention to stereochemistry.
The image contains four chemical reactions, each involving a distinct organic compound as the starting material and a different reagent or condition: 1. The first reaction starts with a bicyclic compound with three methyl groups (Me) attached. This compound reacts with bromine (\( \text{Br}_2 \)) under light (\( h\nu \)). 2. The second reaction involves a cyclobutane with two hydroxyl groups (\( \text{OH} \)) on either end of a chain. It reacts with hydrobromic acid (\( \text{HBr} \)) in two equivalents. 3. The third reaction shows a bicyclic compound with a hydroxyl group (\( \text{OH} \)) and a hydrogen atom (H) on a six-membered ring. It reacts with thionyl chloride (\( \text{SOCl}_2 \)) and a base. The reaction assumes an \( \text{S}_\text{N}2 \) mechanism. 4. The fourth reaction starts with a bicyclic compound with multiple methyl groups (\( \text{Me} \)) and a hydroxyl group (\( \text{OH} \)). This compound reacts with hydrochloric acid (\( \text{HCl} \)). Each reaction arrow indicates a chemical transformation under specified conditions.
Transcribed Image Text:The image contains four chemical reactions, each involving a distinct organic compound as the starting material and a different reagent or condition: 1. The first reaction starts with a bicyclic compound with three methyl groups (Me) attached. This compound reacts with bromine (\( \text{Br}_2 \)) under light (\( h\nu \)). 2. The second reaction involves a cyclobutane with two hydroxyl groups (\( \text{OH} \)) on either end of a chain. It reacts with hydrobromic acid (\( \text{HBr} \)) in two equivalents. 3. The third reaction shows a bicyclic compound with a hydroxyl group (\( \text{OH} \)) and a hydrogen atom (H) on a six-membered ring. It reacts with thionyl chloride (\( \text{SOCl}_2 \)) and a base. The reaction assumes an \( \text{S}_\text{N}2 \) mechanism. 4. The fourth reaction starts with a bicyclic compound with multiple methyl groups (\( \text{Me} \)) and a hydroxyl group (\( \text{OH} \)). This compound reacts with hydrochloric acid (\( \text{HCl} \)). Each reaction arrow indicates a chemical transformation under specified conditions.
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