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 Protonatin of amines to form ammonium salts |
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 Alkylation of amines
Note that you must have a primary amine and a primary or secondary alkyl bromide
for this reaction |
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 Alkylation of amines
Note that you must have a tertiary amine and a primary or secondary alkyl bromide
for this reaction |
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 Acylation of amines
Note that you must have a primary amine |
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 |
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 X = OH, OR, or NR2 |
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 Preparation of primary alkyl amines by alkylation of
ammonia |
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 Preparation of primary alkyl amines by reduction of
azides
(must start with primay or secondary alkyl bromide) |
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 Preparation of primary alkyl amines by reduction of
nitriles
(must start with primay or secondary alkyl bromide) |
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 Preparation of primary aromatic amines by reduction of
nitroarenes
(Primary arylamine is formed) |
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 Diazotization of primary aromatic amines |
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