Reagents Available a. CH2=CHCH2CI, AICI3 b. CH2Br2, OH c. CH3CH2COCI, AICI3 d. H2, Pt e. NBS, CCI4 f. K* tBuO g. CO, HCI, CUCI/AICI3 h. CH3CH2CH2COCI, AICI3 i. BrCH2CH2Br, OH- j. CH;CH2CI, AICI3 k. RCO3H I. H3O* Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol).

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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Reagents Available
g. CO, HCI, CUCI/AICI3
h. CH3CH2CH2COCI, AICI3
i. BrCH2CH2Br, Он
j. CH3CH2CI, AICI3
k. RCO3H
I. H3O*
a. CH2=CHCH,CI, AICI3
b. CH2B12, OH
c. CH3CH2COCI, AICI3
d. H2, Pt
e. NBS, CCI4
f. K* tBuO
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.
Transcribed Image Text:Reagents Available g. CO, HCI, CUCI/AICI3 h. CH3CH2CH2COCI, AICI3 i. BrCH2CH2Br, Он j. CH3CH2CI, AICI3 k. RCO3H I. H3O* a. CH2=CHCH,CI, AICI3 b. CH2B12, OH c. CH3CH2COCI, AICI3 d. H2, Pt e. NBS, CCI4 f. K* tBuO 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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