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).
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).
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).
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