Answer Happy

Design an efficient strategy for the following two-step synthesis. To answer this question, simply type the letter of the "Reagent Identifier" from the Table below into the appropriate boxes for Steps 1 and 2 (that is, just type "A", "B", "C", etc). Next, type the IUPAC name of the compound you make along the way in its box. In the table, you will find a list of possible reagents to use in solving this synthesis problem. starting material Reagent Identifier A B C D Step 1 E F G H 1 J K L M Stable compound Reagent 1) BH/THF 2) H₂O,/NaOH/H₂O Concentrated H₂SO/heat HgSO/H.SO/H,O OsO/NMO CH₂₂/Zn(Cu) HBr/peroxides HCI 1) Hg(OAc),/H,O/THF 2) NaBH, 1) 3 NaNH, 2) NH,Cl(aq) CHCI,/(CH₂) COK H₂/P-2 catalyst H₂O/ heat 2 NaNH, target molecule Br (Step 2)

Reagent Identifier A B C D E F G H I J K L M N 0 Р Q R S T U V W X Reagent 1) BH/THF 2) H₂O₂/NaOH/H,O Concentrated H₂SO/heat HgSO /H,SO/H,O OsO/NMO CH₂₂/Zn(Cu) HBr/peroxides HCI 1) Hg(OAc),/H,O/THF 2) NaBH 1) 3 NaNH, 2) NH,Cl(ag) CHCI,/(CH₂) COK H₂/P-2 catalyst H₂O'/heat 2 NaNH, Br₂ H₂/Lindlar's catalyst t-BuOK/t-BuOH NBS/ light Br./H₂O H₂/Pt Br₂/light Li / EtNH, EtONa/EtOH HBr Other reagent that is not listed Note: if you have trouble naming this intermediate look in chapter 4, somewhere between pages 148 - 161. Sorry I can't give more of a hint than that. The reagent I would use in Step 1 is (just type the letter): IUPAC name of stable compound made along the way is: The reagent I would use in Step 2 is (just type the letter):