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 Creates a vicinal halide (anti addition) |
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 syn addition |
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 Creates an alkyl halide following Markovnikov's rule. |
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 Creates a Markovnikov alcohol |
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 Creates an anti-Markovnikov alcohol |
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 Alkenes react with peracides to form epoxodies/oxiranes
through a syn addition. |
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 Yields two carbonyl compounds. |
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 React with cold potassium permanganate to form vicinal
diols through a syn addition. |
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 Eliminates water to form the most stable alkene (use
Zaitsev's rule) |
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 Eliminates HX to form the most stable alkene (anti
elimination) (use Zaitsev's rule) |
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