5. For each of the following reactions, predict the major product(s). Include stereochemistry where appropriate. Note: benzene rings/aromatic rings are a different functional group than alkene and do not react in addition reactions. HCI Br₂ H₂O H₂SO H₂O 1. BH, THF 2. NGOH, HO, 1. Hg(OAc)₂ H₂O 2. NaBH₂ 1.9-BBN 2. NaOH H₂O₂ B₂ 1. mCPBA 2. TSOH H₂O H₂O* HBr (excess)

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter19: Enolate Anions And Enamines
Section19.9: Crossed Enolate Reactions Using Lda
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5. For each of the following reactions, predict the major product(s). Include stereochemistry where appropriate. Note:
benzene rings/aromatic rings are a different functional group than alkene and do not react in addition reactions.
B₂
HCI
H₂O
H₂SO
H₂O
1. BH, THF
2. NGOH, HO,
1. Hg(OAc)₂
H₂O
2. NaBH₂
1.9-BBN
2. NaOH
H₂O₂
Br₂
1. mCPBA
2. TSOH
H₂O
H₂O*
HBr (excess)
Transcribed Image Text:5. For each of the following reactions, predict the major product(s). Include stereochemistry where appropriate. Note: benzene rings/aromatic rings are a different functional group than alkene and do not react in addition reactions. B₂ HCI H₂O H₂SO H₂O 1. BH, THF 2. NGOH, HO, 1. Hg(OAc)₂ H₂O 2. NaBH₂ 1.9-BBN 2. NaOH H₂O₂ Br₂ 1. mCPBA 2. TSOH H₂O H₂O* HBr (excess)
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