CH3 Reagents Available a. CH₂=CHCH₂CI, AICI 3 b. CH₂Br₂, OH™ C. CH3CH₂COCI, AICI 3 d. H₂, Pt e. NBS, CCl4 f. K* tBuO™ g. CO, HCI, CUCI/AICI 3 h. CH3CH₂CH₂COCI, AICI 3 i. BrCH₂CH₂Br, OH- j. CH3CH₂CI, AICI 3 k. RCO3H I. H3O+ Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol). Select reagents from the table in the order that you wish to use them, i.e. aced; do not include punctuation or spaces. If more than one route exists, choose the shorter one; in no case will a synthesis require more than 5 steps.
CH3 Reagents Available a. CH₂=CHCH₂CI, AICI 3 b. CH₂Br₂, OH™ C. CH3CH₂COCI, AICI 3 d. H₂, Pt e. NBS, CCl4 f. K* tBuO™ g. CO, HCI, CUCI/AICI 3 h. CH3CH₂CH₂COCI, AICI 3 i. BrCH₂CH₂Br, OH- j. CH3CH₂CI, AICI 3 k. RCO3H I. H3O+ Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol). Select reagents from the table in the order that you wish to use them, i.e. aced; do not include punctuation or spaces. If more than one route exists, choose the shorter one; in no case will a synthesis require more than 5 steps.
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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Question
![O
Reagents Available
a. CH₂=CHCH₂CI, AICI 3
CH3
b. CH₂Br₂, OH™
C. CH3CH₂COCI, AICI 3
d. H₂, Pt
e. NBS, CCI4
f. K* tBuO™
g. CO, HCI, CUCI/AICI3
h. CH3CH₂CH₂COCI, AICI 3
i. BrCH₂CH₂Br, OH-
j. CH3CH₂CI, AICI 3
k. RCO3H
I. H3O+
Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol).
Select reagents from the table in the order that you wish to use them, i.e. aced; do not include punctuation or spaces.
If more than one route exists, choose the shorter one; in no case will a synthesis require more than 5 steps.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F08f90593-d3a7-4e16-881f-a11620f884fb%2Fc9f907d3-726c-4bf3-b646-76e1ef7f44a9%2Fs2g5vzp_processed.jpeg&w=3840&q=75)
Transcribed Image Text:O
Reagents Available
a. CH₂=CHCH₂CI, AICI 3
CH3
b. CH₂Br₂, OH™
C. CH3CH₂COCI, AICI 3
d. H₂, Pt
e. NBS, CCI4
f. K* tBuO™
g. CO, HCI, CUCI/AICI3
h. CH3CH₂CH₂COCI, AICI 3
i. BrCH₂CH₂Br, OH-
j. CH3CH₂CI, AICI 3
k. RCO3H
I. H3O+
Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol).
Select reagents from the table in the order that you wish to use them, i.e. aced; do not include punctuation or spaces.
If more than one route exists, choose the shorter one; in no case will a synthesis require more than 5 steps.
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