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Hydrocarbon Derivatives Amines, Amides, & Amino Acids Amines • Contain a N • General Format: RNH2 • -NH2 = amino group (Remember, N has a bonding capacity of 3.) • Since molecules can contain H bonded to N, hydrogen bonding occurs, but it is weaker than hydrogen bonding in alcohols and carboxylic acids. • Amines smell really, really bad. Table R R’ • Shows format RNR” This is a 3 amine. H • 1 amines: RNH H • 2 amines: RNR’ Naming Amines • • • • Find name of base hydrocarbon. Drop final –e. Add “-amine.” If necessary, use a # in front of name to give location of amino group. H H H HCCNH H H H H H H HCCCNH H H H Ethanamine 1-propanamine < H H H N H HCCCH H H H CH2CH2CH2 NH2 NH2 2-propanamine 1,3-propanediamine NH2 NH2 CHCH2CH2CH 1,1,4,4-butanetetraamine NH2 NH2 Examples of amines • • • • • PABA Caffeine Novacain B-vitamins Preparation of dyes Amides • Contain a carbonyl group, >C=O, & an amino group, NH2 group. • The amino group is bonded to the C of the carbonyl group. • Links amino acids together. Table R O R’ = = O • General Format: RCNH2 or RCNH • It’s like taking a carboxylic acid, RCOOH, and replacing the -OH with NH2. • • RCO-NH2. In this case, no # is needed in name. Amide group is at end of molecule. Naming Amides • Find the name of the alkane with the same # of C’s, drop the final –e, & replace it with –amide. = H O HCCNH 2 H Ethanamide = O CH3CH2CNH2 Propanamide Properties of Amides • Have strong hydrogen bonding, so high boiling points. • Simple amides are solids at room temp. • Smaller amides are very soluble in water. Amino Acids • • • • Have to recognize them. Contain a carboxyl group (-COOH). Contain an amine group (-NH2). Amino group is on the C next to the carboxyl group. • Don’t have to name them. NH2 O CH3CC OH NH2 O CH2C OH Amino Acids alanine glycine