Devise a route to convert propene to propanone. Specify, in order, the reagents you would use. The reaction may require more than one step. If there is more than one feasible route, show only one. a NBS b H₂, Pd c H₂O, H₂SO4 d PCC e Br₂ in H₂O f K₂Cr₂O7, H₂SO4, H₂O, heat g Cl₂, heat or light h Cl₂ i HCI j NaOH k OsO4/H₂O2 I 1. BH3 2. H₂O2, NaOH m SOCI₂, pyridine n HBr o Br₂, Specify reagents using letters from the table, first reagent on the left. Example: ab The reagents are (in order of use):

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter8: Haloalkanes, Halogenation, And Radical Reactions
Section8.7: Radical Autoxidation
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Devise a route to convert propene to propanone.
Specify, in order, the reagents you would use. The reaction may require more than one step. If there is more than one feasible route, show only one.
a NBS
b H₂, Pd
c H₂O, H₂SO4
d PCC
e Br₂ in H₂O
f K₂Cr₂O7, H₂SO4,
H₂O, heat
g Cl₂, heat or light
h Cl2
i HCI
j NaOH
k OsO4/H₂O2
1. BH3
2. H₂O2, NaOH
m SOCI2₂, pyridine
I
n
Specify reagents using letters from the table, first reagent on the left. Example: ab
The reagents are (in order of use):
HBr
o Br2,
Transcribed Image Text:Devise a route to convert propene to propanone. Specify, in order, the reagents you would use. The reaction may require more than one step. If there is more than one feasible route, show only one. a NBS b H₂, Pd c H₂O, H₂SO4 d PCC e Br₂ in H₂O f K₂Cr₂O7, H₂SO4, H₂O, heat g Cl₂, heat or light h Cl2 i HCI j NaOH k OsO4/H₂O2 1. BH3 2. H₂O2, NaOH m SOCI2₂, pyridine I n Specify reagents using letters from the table, first reagent on the left. Example: ab The reagents are (in order of use): HBr o Br2,
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