10. Amines and Amides

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10 Terms

1
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What is an Amine?

  • An ammonia molecule that has one (or more)

    of its hydrogens replaced by an alkyl group

  • General Formula: CₙH₂ₙ₊₃N

  • Functional Group: NH₂

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How do you determine if an Amine is Primary (1°), Secondary (2°), or Teritiary (3°)?

  1. one alkyl group attached to the N

  2. two alkyl groups attached

  3. three alkyl groups attached

3
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What are an Amine’s Properties?

  • strong odours

  • amines found in urine, decaying flesh

  • small ones soluble in water

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What are Amides?

  • carbonyl group bonded with an amine

    • carboxyamide functional group

  • carboxylic acid + ammonia, primary/secondary amines to produce amides

<ul><li><p>carbonyl group bonded with an amine </p><ul><li><p>carboxyamide functional group</p></li></ul></li><li><p>carboxylic acid + ammonia, primary/secondary amines to produce amides</p></li></ul><p></p>
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What is the General Formula for Amides?

CₙH₂ₙ₊₁NO

6
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How do you form Amines?

alkyl halide (carbon chain with a halogen) + ammonia

<p>alkyl halide (carbon chain with a halogen) + ammonia</p>
7
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<h2 id="6081ac6d-90dd-408d-b0e3-686af90a71f4" data-toc-id="6081ac6d-90dd-408d-b0e3-686af90a71f4" collapsed="false" seolevelmigrated="true">What is the classification of Amine presented in the photo? What can <u>further</u> do with it?</h2><p></p>

What is the classification of Amine presented in the photo? What can further do with it?

  1. it is a primary amine

  2. by adding another alkyl halide, we can create a secondary amine

8
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<h2 id="bbb874f9-64f3-4e59-aa75-18240089664d" data-toc-id="bbb874f9-64f3-4e59-aa75-18240089664d" collapsed="false" seolevelmigrated="true">What classification is presented here?</h2><p></p>

What classification is presented here?

a secondary amine

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How can you create Amides?

carboxylic acid + ammonia/primary or secondary amine

a condensation reaction

<p>carboxylic acid + ammonia/primary or secondary amine</p><p><em>a </em><strong><em>condensation</em></strong><em> reaction</em></p>
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Reduction of Nitrobenzene

First Step

  1. Nitrobenzene, C₆H₅NO₂, is dissolved in a mixture of tin and concentrated HCl

  2. the mixture is heated under reflux in a water bath

  3. phenylammonium ions, C₆H₅NH₃⁺

Second Step

  1. phenylammonium + NaOH removes the H⁺ (creates water) and creates phenylamine, C₆H₅NH₂

<p>First Step</p><ol><li><p>Nitrobenzene, C₆H₅NO₂, is dissolved in a mixture of tin and concentrated HCl</p></li><li><p>the mixture is heated under reflux in a water bath</p></li><li><p>phenylammonium ions, C₆H₅NH₃⁺</p></li></ol><p>Second Step</p><ol><li><p>phenylammonium + NaOH removes the H⁺ (creates water) and creates phenylamine, C₆H₅NH₂</p></li></ol><p></p>