How can the following conversion be achieved? CH3 CH3 он O 1) BH3/THF 2) H202, H20, OH" 1) Hg(OAc)2/H20, THF 2) NaBH4 H2O/H2SO4 Both A and B Both B and C
How can the following conversion be achieved? CH3 CH3 он O 1) BH3/THF 2) H202, H20, OH" 1) Hg(OAc)2/H20, THF 2) NaBH4 H2O/H2SO4 Both A and B Both B and C
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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![**Question 8:**
How can the following conversion be achieved?
\[ \text{Conversion: Cyclohexane with a methyl group (CH}_3) \rightarrow \text{Cyclohexanol with a methyl group (CH}_3\text{) attached} \]
**Options:**
- A)
1) \( \text{BH}_3/\text{THF} \)
2) \( \text{H}_2\text{O}_2, \text{H}_2\text{O, OH}^- \)
- B)
1) \( \text{Hg(OAc)}_2/\text{H}_2\text{O, THF} \)
2) \( \text{NaBH}_4 \)
- C) \( \text{H}_2\text{O}/\text{H}_2\text{SO}_4 \)
- D) Both A and B
- E) Both B and C
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Transcribed Image Text:**Question 8:**
How can the following conversion be achieved?
\[ \text{Conversion: Cyclohexane with a methyl group (CH}_3) \rightarrow \text{Cyclohexanol with a methyl group (CH}_3\text{) attached} \]
**Options:**
- A)
1) \( \text{BH}_3/\text{THF} \)
2) \( \text{H}_2\text{O}_2, \text{H}_2\text{O, OH}^- \)
- B)
1) \( \text{Hg(OAc)}_2/\text{H}_2\text{O, THF} \)
2) \( \text{NaBH}_4 \)
- C) \( \text{H}_2\text{O}/\text{H}_2\text{SO}_4 \)
- D) Both A and B
- E) Both B and C
**Submit Instructions:**
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Expert Solution

Step 1
Option A is the correct choice.
Because it gives the less substituted alcohol. The reaction is known as Hydroboration oxidation reaction.
It follows the Anti-Markonikov rule to give the major product.
In rest of the given options Markonikov rule is followed.
According to Markonikov rule, generation of the positive charge always takes place at more substituted carbon atom . So that nucleophile attaches with that carbon to give the more substituted product.
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