Please predict the outcome of each reaction below: Type you answer as a letter: A, B, ..., or F. Problem 1: https://doi.org/10.1021/ol101705j Answer to Problem 1: Hint 1. Assume the reaction can ONLY occur at the MOST ELECTRON RICH double bond. Hint 2. Assume the reaction can ONLY occur from the least sterically hindered side of the molecule. Draw or build a 3-dimentional conformation to support your answer. 1 equivalent m-CPBA ? A H B C D E F

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter19: Eas: Electrophilic Aromatic Substitution
Section: Chapter Questions
Problem 10E
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Please predict the outcome of each reaction below: Type you answer as a letter: A, B, ...., or F.
Please predict the outcome of each reaction below:
Type you answer as a letter: A, B, ..., or F.
Problem 1: https://doi.org/10.1021/ol101705j
Answer to Problem 1:
Hint 1. Assume the reaction can ONLY occur at the MOST ELECTRON RICH double bond.
Hint 2. Assume the reaction can ONLY occur from the least sterically hindered side of the molecule. Draw or build a 3-dimentional conformation to support your answer.
1 equivalent
m-CPBA
?
A
H
B
C
D
E
F
Transcribed Image Text:Please predict the outcome of each reaction below: Type you answer as a letter: A, B, ..., or F. Problem 1: https://doi.org/10.1021/ol101705j Answer to Problem 1: Hint 1. Assume the reaction can ONLY occur at the MOST ELECTRON RICH double bond. Hint 2. Assume the reaction can ONLY occur from the least sterically hindered side of the molecule. Draw or build a 3-dimentional conformation to support your answer. 1 equivalent m-CPBA ? A H B C D E F
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