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Stack #4567052
| Question | Answer |
|---|---|
| Ozonolysis | Reagents: Ozone, DMS |
| Ozonolysis | Outcome: Splits the double bond and replaces each C=C with C=O |
| Catalytic Hydrogenation | Reagents: H2, Catalyst (Pt) |
| Catalytic Hydrogenation | Outcome: Removes double bond with syn addition |
| Hydrohalogenation | Reagents: HX (H and halogen) |
| Hydrohalogenation | Outcome: Markovnikov addition |
| Hydration | Reagents: H2O, acid |
| Hydration | Outcome: Markovnikov addition |
| Halogenation | Reagents: X2 (halogens) |
| Halogenation | Outcome: Markovnikov addition |
| Acid-catalyzed Hydration | Reagents: H3O+ (acid) |
| Acid-catalyzed Hydration | Outcome: Acid protonates double bond; water binds to carbocation; deprotonation leaves OH. Markovnikov addition |
| Oxymercuration-Demercuration | Reagents: Hg(OAc)2, nucleophile-H; NaBH4 |
| Oxymercuration-Demercuration | Outcome: Markovnikov addition without carbocation rearrangement |
| Hydroboration-Oxidation | Reagents: 1) BH3, THF 2) H2O2, NaOH |
| Hydroboration-Oxidation | Outcome: Anti-Markovnikov syn addition |
| Syn Dihydroxylation | Reagents: OsO4, NMO or cold KMnO4 |
| Syn Dihydroxylation | Outcome: Syn addition of OH on both sides |
| Epoxidation | Reagents: Peroxyacetic acid or MCPBA |
| Epoxidation | Outcome: Forms an epoxide ring |
| Anti Dihydroxylation | Reagents: Aqueous acid, epoxide required |
| Anti Dihydroxylation | Outcome: Anti addition of OH on opposite sides |