10. Write out the mechanism (intermediate/transition state) for this reaction. Indicate stereochemistry in product. H Br CH3 NaN3 S₁2 For the following use ONLY reactions we have studied in slas

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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Comp
How
Carte EDF Tuncte with cest
10. Write out the mechanism (intermediate/transition state) for this reaction. Indicate
stereochemistry in product.
For the following
ONL
fides for prep
H
Br
Ed to give a CaHaBr F compour
CH3
NaN 3
S₁2
ferent reactions of acetophenone (reagent, produch
12-methyl-2-balanol, using a different starting material for
nctional groups and/or
Transcribed Image Text:Comp How Carte EDF Tuncte with cest 10. Write out the mechanism (intermediate/transition state) for this reaction. Indicate stereochemistry in product. For the following ONL fides for prep H Br Ed to give a CaHaBr F compour CH3 NaN 3 S₁2 ferent reactions of acetophenone (reagent, produch 12-methyl-2-balanol, using a different starting material for nctional groups and/or
9. Compound X, C40H67Br2F, reacts with excess H2/Pd to give a C40H73Br2F compound.
How many rings are in X?
How many double bonds are in X?
Show your work.
use ONLY reactions we have studied in class. Check your notes
lides for preparations and reactions of relevant functional
Transcribed Image Text:9. Compound X, C40H67Br2F, reacts with excess H2/Pd to give a C40H73Br2F compound. How many rings are in X? How many double bonds are in X? Show your work. use ONLY reactions we have studied in class. Check your notes lides for preparations and reactions of relevant functional
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