Nucleophilic Properties of Amines

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10 Terms

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primary amines react with acid anyhydrides to form

a secondary amide and an ammonium salt

<p><span>a secondary amide and an ammonium salt</span></p>
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<p><span>Primary amines can act as</span></p>

Primary amines can act as

nucleophile in nucleophilic addition-elimination reactions. 

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primary amines also react with acyl chlorides to form

a secondary amide and an ammonium salt 

<p><span>a secondary amide and an ammonium salt&nbsp;</span></p>
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<p>Mechanisms</p>

Mechanisms

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ammonia and halogenoalkanes undergo….. to produce an amine. 

what is needed

nucleophilic substitution reaction

<p><span>nucleophilic substitution reaction</span></p>
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However, if there is excess halogenoalkane when ammoni and halgeonoalkanes react what happens

the primary amine can also act as a nucleophile. This means it can react again to produce a secondary amine. 

 

That secondary amine can then act as a nucleophile, and so on

<p>the primary amine can also act as a nucleophile. This means it can react again to produce a secondary amine.&nbsp;</p><p>&nbsp;</p><p>That secondary amine can then act as a nucleophile, and so on</p>
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quaternary ammonium ion

When nitrogen is bonded to four alkyl groups

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quaternary ammonium salt

When quaternary ammonium ions form a lattice with anions

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When a quaternary ammonium ion has one long alkyl chain, what are the ends

it has a polar end and a non-polar end. 

 

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quaternary ammonium ion useful properties:

it’s often used in cleaning products, as a cationic surfactant

<p><span>it’s often used in cleaning products, as a&nbsp;</span><strong>cationic surfactant</strong><span>.&nbsp;</span></p>