1 BH, THE 25 C 2. HyO. OH HyC OH CH3CHCHCH,CH, CH3 2-Methyl-3-pentanol CHC-CHCH,CH, 2-Methyl-2-pentene 1. BH, THE 160 °C 2. HyOp. OH CHJCHCH;CH2CH2OH 4-Methyl-1-pentanel
1 BH, THE 25 C 2. HyO. OH HyC OH CH3CHCHCH,CH, CH3 2-Methyl-3-pentanol CHC-CHCH,CH, 2-Methyl-2-pentene 1. BH, THE 160 °C 2. HyOp. OH CHJCHCH;CH2CH2OH 4-Methyl-1-pentanel
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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Hydroboration of 2-methyl-2-pentene at 25°C, followed by oxidation with alkaline H2o2, yields 2-methyl-3-pentanol, but hydroboration at 160°C followed by oxidation yields 4-methyl-1-pentanol. Suggest a mechanism.
![1 BH, THE 25 C
2. HyO. OH
HyC OH
CH3CHCHCH,CH,
CH3
2-Methyl-3-pentanol
CHC-CHCH,CH,
2-Methyl-2-pentene
1. BH, THE 160 °C
2. HyOp. OH
CHJCHCH;CH2CH2OH
4-Methyl-1-pentanel](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc2b88e64-1f10-4b4e-9a98-e84f4402330c%2F27049db3-d147-4893-9ef9-a33a30923c36%2Fdqsug75_processed.png&w=3840&q=75)
Transcribed Image Text:1 BH, THE 25 C
2. HyO. OH
HyC OH
CH3CHCHCH,CH,
CH3
2-Methyl-3-pentanol
CHC-CHCH,CH,
2-Methyl-2-pentene
1. BH, THE 160 °C
2. HyOp. OH
CHJCHCH;CH2CH2OH
4-Methyl-1-pentanel
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