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Key Concepts—Alcohols, Ethers, and Epoxides

Besides rearranging, a carbocation can also react with a nucleophile (7.13) and a base (8.6). [Pg.352]

Tosylates undergo either substitution or elimination, depending on the reagent (9.13B). [Pg.354]

Elimination is carried out with a strong base, so the mechanism isE2. [Pg.354]

Only one reaction is useful cleavage with strong acids (9.14). [Pg.354]

Epoxide rings are opened with nucleophiles Nu and acids HZ (9.15). [Pg.354]

See other pages where Key Concepts—Alcohols, Ethers, and Epoxides is mentioned: [Pg.352] [Pg.353]

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Epoxide alcohol

Ethers and Epoxides

Key concepts