CHAPTER 23 - AMINES

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16 Terms

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Preparation of amines (23.6)

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<p>[1] Direct nucleophilic substitution with NH3</p><p>and amines (23.6A) </p>

[1] Direct nucleophilic substitution with NH3

and amines (23.6A)

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<p>[2] Gabriel synthesis (23.6A)</p>

[2] Gabriel synthesis (23.6A)

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<p>[3] Reduction methods (23.6B)</p>

[3] Reduction methods (23.6B)

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<p>[4] Reductive amination (23.6C)</p><p>d</p>

[4] Reductive amination (23.6C)

d

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Reactions of amines

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<p>[1] Reaction as a base (23.8)</p>

[1] Reaction as a base (23.8)

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<p>[2] Nucleophilic addition to aldehydes and ketones (23.10)</p><p>With 1° amines:</p>

[2] Nucleophilic addition to aldehydes and ketones (23.10)

With 1° amines:

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<p>[2] Nucleophilic addition to aldehydes and ketones (23.10)</p><p>With 2° amines:</p>

[2] Nucleophilic addition to aldehydes and ketones (23.10)

With 2° amines:

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<p>3] Nucleophilic substitution with acid chlorides and anhydrides (23.10)d</p>

3] Nucleophilic substitution with acid chlorides and anhydrides (23.10)d

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<p>[4] Hofmann elimination (23.11) </p>

[4] Hofmann elimination (23.11)

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<p>[5] Reaction with nitrous acid (23.12) </p><p>With 1° amines:</p>

[5] Reaction with nitrous acid (23.12)

With 1° amines:

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<p>[5] Reaction with nitrous acid (23.12) </p><p>With 2° amines:</p>

[5] Reaction with nitrous acid (23.12)

With 2° amines:

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Reactions of diazonium salts

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<p>[1] Substitution reactions (23.13)</p>

[1] Substitution reactions (23.13)

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<p>[2] Coupling to form azo compounds (23.14) </p>

[2] Coupling to form azo compounds (23.14)

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