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. D OH Br OH OH conc H₂SO heat 1) TSCL pyndine 2) BUCK BUCK 1-BUCK conc H₂SO, heat

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Chapter1: Chemical Foundations
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G.23.

 

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.
0 Br
0
D
OH
*-05-05-0
Br
OH
D OH
D
D
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.
conc H₂SO
heat
Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that
apply.
DHO
1) TSCL pyndine
2)BUOK
D
BUCK
O
DHO
O
1-BUCK
conc. H₂SO,
heat
DHO.
D
O
.
D
Hox 1) TCL, pyndine
211 BOK
Hot
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.
BUCK
Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that
apply.
ля
NaOH
1) TSCL, pyridine
2) NaOH
conc H₂SO,
heat
1-BUCK
NaOH
u:
1-BUCK
BUCK
NaOt
Nat
conc H₂SO,
heat
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. 0 Br 0 D OH *-05-05-0 Br OH D OH D D 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. conc H₂SO heat Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that apply. DHO 1) TSCL pyndine 2)BUOK D BUCK O DHO O 1-BUCK conc. H₂SO, heat DHO. D O . D Hox 1) TCL, pyndine 211 BOK Hot 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. BUCK Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that apply. ля NaOH 1) TSCL, pyridine 2) NaOH conc H₂SO, heat 1-BUCK NaOH u: 1-BUCK BUCK NaOt Nat conc H₂SO, heat
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