compound d Mg, ether compound c HBr, H₂0₂ compound b K* IBUO compound a Br₂, hy RCO₂H compound h CHBr3, (CH3)3CO¹K* comp

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compound d Mg, ether compound c HBr, H₂0₂ compound b K* IBUO compound a Br₂, hy RCO₂H compound h CHBr3, (CH3)3CO¹K* comp

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Compound D Mg Ether Compound C Hbr H 0 Compound B K Ibuo Compound A Br Hy Rco H Compound H Chbr3 Ch3 3co K Comp 1
Compound D Mg Ether Compound C Hbr H 0 Compound B K Ibuo Compound A Br Hy Rco H Compound H Chbr3 Ch3 3co K Comp 1 (18.71 KiB) Viewed 49 times
Compound D Mg Ether Compound C Hbr H 0 Compound B K Ibuo Compound A Br Hy Rco H Compound H Chbr3 Ch3 3co K Comp 2
Compound D Mg Ether Compound C Hbr H 0 Compound B K Ibuo Compound A Br Hy Rco H Compound H Chbr3 Ch3 3co K Comp 2 (17.72 KiB) Viewed 49 times
compound d Mg, ether compound c HBr, H₂0₂ compound b K* IBUO compound a Br₂, hy RCO₂H compound h CHBr3, (CH3)3CO¹K* compound g H₂SO4 compound f H₂O, H₂O* compound e
This synthesis scheme was designed using the roadmaps found in the appendix of your textbook. Follow through the scheme, and draw the structure(s) of compound b. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Consider E/Z stereochemistry of alkenes. Draw the Grignard reagent as a covalent magnesium bromide. . If enantiomers are formed, draw both. Separate structures with + signs from the drop-down menu. . . . D
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