QUESTION 3 Think retrosynthetically. Consider the bonding patterns and connectivity in your product and the new piece that was added. Which organometallic reagent was used to form the new C-C bond? A) C) MgBr OH MgBr D) MgBr MgBr O B O D O 0 0 0

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Only do questions #3 the other questions is only for reference!!!

QUESTION 1
Consider the 2-step synthesis problem shown below to answer questions 1-4.
OH
Reagent
Reagent
HO
Intermediate
Product
Br
Number the carbons in your starting material. Identify the corresponding carbons in your product and number them accordingly. A new C-C bond was made. Click on that new C-C bond in the image of the final product shown
below.
HO
Selected Coordinates
Clear
Transcribed Image Text:QUESTION 1 Consider the 2-step synthesis problem shown below to answer questions 1-4. OH Reagent Reagent HO Intermediate Product Br Number the carbons in your starting material. Identify the corresponding carbons in your product and number them accordingly. A new C-C bond was made. Click on that new C-C bond in the image of the final product shown below. HO Selected Coordinates Clear
QUESTION 3
Think retrosynthetically. Consider the bonding patterns and connectivity in your product and the new piece that was added. Which organometallic reagent was used to form the new C-C bond?
A)
B)
C) MgBr
OH
MgBr
D)
MgBr
MgBr
O O O O
Transcribed Image Text:QUESTION 3 Think retrosynthetically. Consider the bonding patterns and connectivity in your product and the new piece that was added. Which organometallic reagent was used to form the new C-C bond? A) B) C) MgBr OH MgBr D) MgBr MgBr O O O O
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