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Ch 13 Carboxylic Acids, Esters, Amines and Amides SWBAT: Name/Draw compounds with functional groups Describe/Explain properties of functional groups Complete/Show reactions of functional groups
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Chapter 13.4 Amines
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Amines They are derivatives of ammonia NH 3 H-groups are replaced by alkyl or aromatic groups
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Subclasses of Amines
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Naming Amines Similar to ether… List the alkyl groups in alpha order No gaps Ends in -amine methylamine dimethylamine
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Practice ethylmethylpropylamine ethyldimethylamine triphenylamine
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Aromatic Amines Aromatic amines use the name aniline Amino bearing Carbon is C#1 2,6-diethyl-4-methylaniline aniline
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Naming Anilines N-ethylaniline Alkyl groups attached to the nitrogen of the aniline are named with the prefix N- followed by the alkyl name N, N-dimethylaniline
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Properties of Amines Boiling Point Amines can have polar N-H bond, so they can form H-bonds But…N is not as electronegative as the O in alcohols…so the H-bonds are weaker! BP is below Alcohol Bp differences among different types of amines! 1 o amines highest BP (2 H-bonds) 2 o amine lower (1 H-bond) 3 o amine lowest (only dipole)
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Properties of Amines Solubility Amine group is polar: soluble in water, will form H-bonds Small amines (1-5 C atoms) are soluble Large amines (<6 C atoms) are not
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Famous Amines Acetyl choline – neurotransmitter Nicotine
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Famous Amines Prozac – Fluoxetine Caffeine
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Reaction of Amines A.1 o and 2 o Amines react as Bases – they accept H + ions like ammonia below: The unpaired valence e- of N attract H+ H + H-N-H + H 2 O → H-N-H + OH - H H NH 3 + H 2 O → NH 4 + + OH - ammonia ammonium ion
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Reacting as a Base Primary Secondary Tertiary amines do not react! dimethyammonium ion Dimethylamine
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Neutralization Reaction Base + Acid → Salt NH 3 + HCl → NH 4 + Cl - Ammonia Ammonium chloride (salt) a) Primary amine CH 3 -NH 2 + HCl → CH 3 -NH 3 + Cl - Methylamine methylammonium chloride b) Similar for secondary amine
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Homework Chapter 13 Page 448 13.34 – 13.44 (even)
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