Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings PowerPoint Lectures for Biology, Seventh Edition Neil Campbell and Jane Reece.

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Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings PowerPoint Lectures for Biology, Seventh Edition Neil Campbell and Jane Reece Lectures by Chris Romero Chapter 4 Biochemistry: The Role of Functional Groups

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Functional groups – Are the chemically reactive groups of atoms within an organic molecule – Give organic molecules distinctive chemical properties CH 3 OH HO O CH 3 OH Estradiol Testosterone Female lion Male lion Figure 4.9

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Important Functional Groups Six functional groups are important in the chemistry of life – Hydroxyl – Carbonyl – Carboxyl – Amino – Sulfhydryl – Phosphate

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Hydroxyl group Polar, thus water-soluble; forms hydrogen bonds FUNCTIONAL GROUP STRUCTURE (may be written HO ) HYDROXYL OH In a hydroxyl group (—OH), a hydrogen atom is bonded to an oxygen atom, which in turn is bonded to the carbon skeleton of the organic molecule. (Do not confuse this functional group with the hydroxide ion, OH –.) C OO C OH Figure 4.10 Is polar as a result of the electronegative oxygen atom drawing electrons toward itself.  Attracts water molecules, helping dissolve organic compounds such as sugars (see Figure 5.3).

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Carbonyl  C=O FUNCTIONAL GROUP STRUCTURE (may be written HO ) HYDROXYL CARBONYL CARBOXYL OH C OO C Figure 4.10 The carbonyl group consists of a carbon atom joined to an oxygen atom by a double bond.

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Carbonyl group A ketone and an aldehyde may be structural isomers with different properties, as is the case with many monosaccharides.

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Carboxyl Weak acid (hydrogen donor); when it loses a hydrogen, it becomes negatively charged (polar) FUNCTIONAL GROUP STRUCTURE (may be written HO ) HYDROXYL CARBONYL CARBOXYL OH When an oxygen atom is double- bonded to a carbon atom that is also bonded to a hydroxyl group, the entire assembly of atoms is called a carboxyl group (— COOH). C OO C OH Figure 4.10

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Carboxyl  Has acidic properties because it is a source of hydrogen ions. The covalent bond between oxygen and hydrogen is so polar that hydrogen ions (H + ) tend to dissociate reversibly; for example,  In cells, found in the ionic form, which is called a carboxylate group. H H C H H C O OH H H C O C OO + H + Figure 4.10

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Examples: Some important functional groups of organic compounds Acetic acid, which gives vinegar its sour tatste NAME OF COMPOUNDS Alcohols (their specific names usually end in -ol) Ketones if the carbonyl group is within a carbon skeleton Aldehydes if the carbonyl group is at the end of the carbon skeleton Carboxylic acids, or organic acids EXAMPLE Propanal, an aldehyde Acetone, the simplest ketone Ethanol, the alcohol present in alcoholic beverages H H H HH CC OH H H H H H H H C C H C C C CCC O H O H H HH H O H Figure 4.10

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Some important functional groups of organic compounds AMINO group Weak base (hydrogen acceptor); when it accepts a hydrogen, it becomes positively charged The amino group (—NH 2 ) consists of a nitrogen atom bonded to two hydrogen atoms and to the carbon skeleton. AMINO SULFHYDRYL PHOSPHATE (may be written HS ) N H H SH O P O OH Figure 4.10

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Amino Some important functional groups of organic compounds  Acts as a base; can pick up a proton from the surrounding solution:  Ionized, with a charge of 1+, under cellular conditions. (nonionized) (ionized) N H H H +N+NH H Figure 4.10

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Sulfhydryl group Ability to form disulfide “bridges”; important in stabilizing protein structure (cysteine) AMINO SULFHYDRYL PHOSPHATE (may be written HS- ) The sulfhydryl group consists of a sulfur atom bonded to an atom of hydrogen; resembles a hydroxyl group in shape. N H H SH O P O OH Figure 4.10

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Phosphate group Acid (hydrogen donor) in solution; usually negatively charged (anionic) Useful in transferring energy between organic molecules (ATP) Present in the backbone of DNA and RNA AMINO SULFHYDRYL PHOSPHATE (may be written HS ) In a phosphate group, a phosphorus atom is bonded to four oxygen atoms; one oxygen is bonded to the carbon skeleton; two oxygens carry negative charges; abbreviated P. The phosphate group (—OPO 3 2– ) is an ionized form of a phosphoric acid group (— OPO 3 H 2 ; note the two hydrogens). N H H SH O P O OH Figure 4.10

Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Some important functional groups of organic compounds Because it also has a carboxyl group, glycine is both an amine and a carboxylic acid; compounds with both groups are called amino acids. Glycine Ethanethiol Glycerol phosphate O C HO C H H N H H H CC SH H H H H H OH CCCOPOO OO HHH O H Figure 4.10