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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
Transcribed Image Text:**Question:**
Identify the correct product(s) for the reaction below.
**Reaction:**
A six-membered cyclohexene (cyclohexane with one double bond) is treated with:
1. Hg(OAc)₂, H₂O
2. NaBH₄
**Possible Products:**
a. Cyclohexane with an -OH group on the opposite carbon of the double bond.
b. Cyclohexane with an -OH group on the adjacent carbon of the double bond, in a secondary position.
c. Cyclohexane with an -OH group reversing the positions on a different carbon from the double bond.
**Options:**
- d. a & b
- e. b & c
- f. a & c
- g. a, b & c
**Explanation:**
The reaction sequence provided describes an oxymercuration-demercuration process, where the double bond in cyclohexene is converted into an alcohol. The typical outcome is Markovnikov addition, where water adds to the more substituted carbon of the alkene, and hydrogen is added to the less substituted carbon.
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