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Functional Groups Group of atoms that gives a family of organic compounds its characteristic chemical and physical properties Alkyl group: derived from alkane by removing a H –R stands for alkyl group in general
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C 2 H 5 OH, ethanol Made industrially and by fermentation –Industrially produced alcohol has noxious substances added Small, simple alcohols tend to be toxic
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Multifunctional Alcohols Several common alcohols have more than one –OH group Ethylene glycol: main ingredient in antifreeze Glycerol: used in lotions –Ingredent in some explosives
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Phenol –OH group on benzene ring –Different chemical properties than other alcohols –Behaves more like an acid First antiseptic –Also causes skin irritation
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Ethers Two alkyl groups attached to same O –Example CH 3 CH 2 -O-CH 2 CH 3 Used mainly as solvent Little chemical reactivity –Insoluble in water –Highly flammable
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Amines Contain N May have 1, 2, or 3 alkyl or aromatic groups Most biological amines are amino acids –Building blocks of proteins
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Aldehydes and Ketones Both contain carbonyl group (C=O) Aldehyde: R-CHO Ketone: R-CO-R’
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Common Aldehydes Change -e ending to -al Produced by oxidation of alcohols Formaldehyde – used as a preservative Larger ones used as fragrances –Benzaldehyde – flavor in maraschino cherries
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Common Ketones Change -e ending to -one Acetone most common ketone –Used primarily as a solvent Produced by oxidation of alcohols
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Amides N bonded directly to carbonyl group Linkage that holds proteins together
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Esters Derived from carboxylic acids and alcohols Tend to be fragrant –Methyl butyrateapple –Ethyl butyratepineapple –Ethyl formaterum –Methyl salicylatewintergreen
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Heterocyclic Compounds Ring compounds that have something other than C in the ring Occur in plants –Alkaloids: basic in solution –Examples: caffeine, morphine, cocaine Form basic structure of DNA
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