'Diazonium ion' presentation slideshows

22.15 Nitrosation of Alkylamines

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22.16 Nitrosation of Alkylamines

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Aromatic Substitution

Aromatic Substitution . Chapter 22. Sections to skip!!. Skip sections 22.1 (most), 22.3, 22.4, and 2.13 through 22.15 Keep 22.16 (review from c. 351, for some of you) Keep 22.17. Problems. In text: 4 - 6 8 - 13 20 - 29 End of Chapter: 1 - 5 9 - 13 . Sect. 22.1 Nomenclature.

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22.15 Nitrosation of Alkylamines

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Nitrite Ion, Nitrous Acid, and Nitrosyl Cation

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Definitions

Definitions. Aliphatic Aromatic Reflux Primary amine Base Substitution Nucleophile Reduction. Amines and their reactions. Describe the preparation of aliphatic amines by substitution of halogenoalkanes . Describe the preparation of aromatic amines by reduction of nitroarenes .

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Azodyes

Azodyes. Azodye made by reacting the diazonium ion of phenylamine and phenol. Azodye made by reacting the diazonium ion of phenylamine and 3 methylphenol. Azodye made by reacting the diazonium ion of phenylamine and napthalen-2-ol.

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Chapter 44 The Sandmeyer Reaction

Chapter 44 The Sandmeyer Reaction. Purpose.

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