Provide a synthesis for the target molecule shown below, starting with an alkyl halide or alcohol of your choice. In each case, show your retrosynthetic analysis, and then provide a complete synthesis, showing all necessary reagents. Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that apply. ☐ ☐ Br HO Br HO Br HO t-BUOK conc. H₂SO4 heat NaOH 1) TSCI, pyridine 2) NaOH NaOH t-BUOK 1) TSCI, pyridine 2) t-BUOK

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Provide a synthesis for the target molecule shown below, starting with an alkyl halide or alcohol of your choice. In each case, show
your retrosynthetic analysis, and then provide a complete synthesis, showing all necessary reagents.
Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that apply.
☐
☐
Br
HO
Br
HO
Br
HO
t-BUOK
conc. H₂SO4
heat
NaOH
1) TSCI, pyridine
2) NaOH
NaOH
t-BUOK
1) TSCI, pyridine
2) t-BUOK
Transcribed Image Text:Provide a synthesis for the target molecule shown below, starting with an alkyl halide or alcohol of your choice. In each case, show your retrosynthetic analysis, and then provide a complete synthesis, showing all necessary reagents. Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that apply. ☐ ☐ Br HO Br HO Br HO t-BUOK conc. H₂SO4 heat NaOH 1) TSCI, pyridine 2) NaOH NaOH t-BUOK 1) TSCI, pyridine 2) t-BUOK
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