7. Predict the product(s) of the following reactions. Note: 18-crown-6 stabilizes cations, but for this reaction, you should be able to ignore it. benzyl phenyl ether OH Br 1. HBr (1 equiv) 2. TsCl 3. KOAc, 18-crown-6 cyclohexene KOH 8. Perform the following synthesis. styrene epoxide 1. HF methyloxirane 2. PCC (XS) HI 9. Provide a detailed mechanism for the following reactions. Note: BF3 acts as a Lewis acid. BF3, E120 1. LDA 2. H trans-cyclohexene glycol HⓇ CHO allyl alcohol OH

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7. Predict the product(s) of the following reactions. Note: 18-crown-6 stabilizes cations, but for this
reaction, you should be able to ignore it.
benzyl phenyl ether
OH
Br
1. HBr (1 equiv)
2. TsCl
3. KOAc, 18-crown-6
cyclohexene
KOH
8. Perform the following synthesis.
styrene epoxide
1. HF
methyloxirane
2. PCC
(XS) HI
9. Provide a detailed mechanism for the following reactions. Note: BF3 acts as a Lewis acid.
BF3, E120
1. LDA
2. H
OH, MeOH
trans-cyclohexene glycol
HⓇ
OH
CHO
allyl alcohol
OH
OH
Transcribed Image Text:7. Predict the product(s) of the following reactions. Note: 18-crown-6 stabilizes cations, but for this reaction, you should be able to ignore it. benzyl phenyl ether OH Br 1. HBr (1 equiv) 2. TsCl 3. KOAc, 18-crown-6 cyclohexene KOH 8. Perform the following synthesis. styrene epoxide 1. HF methyloxirane 2. PCC (XS) HI 9. Provide a detailed mechanism for the following reactions. Note: BF3 acts as a Lewis acid. BF3, E120 1. LDA 2. H OH, MeOH trans-cyclohexene glycol HⓇ OH CHO allyl alcohol OH OH
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