Reagents Available a. CH2=CHCH,CI, AICI3 b. CН-Br2, ОН c. CH3CH2COCI, AICI3 d. H2, Pt e. NBS, CCI, f. K* tBuO g. CO, HCI, CUCI/AICI3 h. CH;CH2CH2COCI, AICI3 i. BrCH2CH2Br, он j. CH;CH2CI, AICI3 k. RCO3H I. H;O* CH3 Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol).

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry
Section4.SE: Something Extra
Problem 40AP: From the data in Figure 4-12 and Table 4-1, estimate the percentages of molecules that have their...
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Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol).

Reagents Available
a. CH2=CHCH,CI, AICI3
b. CН-Br2, ОН
c. CH3CH2COCI, AICI3
d. H2, Pt
e. NBS, CCI4
f. K* tBuO
g. CO, HCI, CUCI/AICI3
h. CH;CH2CH2COCI, AICI3
i. BrCH2CH2Br, он
j. CH;CH2CI, AICI3
k. RCO3H
I. H3O*
CH3
Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol).
Transcribed Image Text:Reagents Available a. CH2=CHCH,CI, AICI3 b. CН-Br2, ОН c. CH3CH2COCI, AICI3 d. H2, Pt e. NBS, CCI4 f. K* tBuO g. CO, HCI, CUCI/AICI3 h. CH;CH2CH2COCI, AICI3 i. BrCH2CH2Br, он j. CH;CH2CI, AICI3 k. RCO3H I. H3O* CH3 Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol).
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