23. In the three-step synthesis below, at least one of the steps would fail as shown. For each step, indicate whether each step would succeed or fail by circling the proper answer. If a step would fail briefly describe why and how you would rectify the synthesis. Succeed or Fall 1. CH.MgBr (1 Equiv) 2. HO' (workup) H₂C OH Succeed or Fal Na Cr₂Or H₂SO H₂C Succeed or Fail H₂C Mon OH 1. SOC (converts -OH to-C 2. Mg(s), Eto 3. & 4. H.O workuol

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23. In the three-step synthesis below, at least one of the steps would fail as shown. For each
step, indicate whether each step would succeed or fail by circling the proper answer. If a
step would fail briefly describe why and how you would rectify the synthesis.
would this step
1. CH.MgBr (1 Equiv)
Succeed or Fal
2. H,O (workup)
force one)
Na:Cr₂O
H₂SO4
OH
1. SOC
(converts-OH to-C
2. Mg(s), EtO
4. H-O (workuol
26.
a. Provide the best reagent(s) for carrying out the reaction below in one step.
b. Show how this reagent can be synthesized from an alkyl bromide with 7 carbons or fewer:
c. Finally, write the mechanism for the product formation in part a.
27. SYNTHESIS! Propose a multistep synthesis for the following transformation. Use the starting
material provided along with any general reagents, protecting groups, and alkyl halides of 6
carbons or fewer (organic reagents/protecting groups may have more than 6 carbons provided
these carbons do not end up in the carbon framework of the final product).
shor
hat
OH
H₂C
Succeed or Fail
force one)
OH
H₂C
Succeed or Fail
(circle one)
Transcribed Image Text:Chemistry please help. thank you 23. In the three-step synthesis below, at least one of the steps would fail as shown. For each step, indicate whether each step would succeed or fail by circling the proper answer. If a step would fail briefly describe why and how you would rectify the synthesis. would this step 1. CH.MgBr (1 Equiv) Succeed or Fal 2. H,O (workup) force one) Na:Cr₂O H₂SO4 OH 1. SOC (converts-OH to-C 2. Mg(s), EtO 4. H-O (workuol 26. a. Provide the best reagent(s) for carrying out the reaction below in one step. b. Show how this reagent can be synthesized from an alkyl bromide with 7 carbons or fewer: c. Finally, write the mechanism for the product formation in part a. 27. SYNTHESIS! Propose a multistep synthesis for the following transformation. Use the starting material provided along with any general reagents, protecting groups, and alkyl halides of 6 carbons or fewer (organic reagents/protecting groups may have more than 6 carbons provided these carbons do not end up in the carbon framework of the final product). shor hat OH H₂C Succeed or Fail force one) OH H₂C Succeed or Fail (circle one)
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