Redo the reaction, but used H,0 with H,SO, as catalyst. Compare the alcohol formed from both methods.

Introduction to General, Organic and Biochemistry
11th Edition
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Chapter15: Chirality: The Handedness Of Molecules
Section: Chapter Questions
Problem 15.39P
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just answer question 2 only

1. Write the structure of the major organic product obtained by hydroboration-
oxidation of each of the following alkenes.
2-Methylpropene
Cyclopentene
а.
b.
C.
cis-2-Butene
3-Ethyl-2-pentene
3-Ethyl-1-pentene
d.
е.
2. Redo the reaction, but used H,0 with H,SO, as catalyst. Compare the alcohol
formed from both methods.
Transcribed Image Text:1. Write the structure of the major organic product obtained by hydroboration- oxidation of each of the following alkenes. 2-Methylpropene Cyclopentene а. b. C. cis-2-Butene 3-Ethyl-2-pentene 3-Ethyl-1-pentene d. е. 2. Redo the reaction, but used H,0 with H,SO, as catalyst. Compare the alcohol formed from both methods.
2. Determine if the following compounds are AROMATIC, ANTIAROMATIC, or NOT
AROMATIC
Cyclodeca-1,3,5,7,9-pentaene
[10]-annulene
Cyclotetradeca-1,3,5,7,9,11,13-heptaene
[14]-annulene
Cyclooctadeca-1,3,5,7,9,11,13,15,17-nonaene
[18]-annulene
Transcribed Image Text:2. Determine if the following compounds are AROMATIC, ANTIAROMATIC, or NOT AROMATIC Cyclodeca-1,3,5,7,9-pentaene [10]-annulene Cyclotetradeca-1,3,5,7,9,11,13-heptaene [14]-annulene Cyclooctadeca-1,3,5,7,9,11,13,15,17-nonaene [18]-annulene
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