1. 1 Chapter 4 Carbon and the Molecular Diversity of Life

2. 2 Carbon Chemistry Carbon is the backbone of biological molecules (macromolecules) All living organisms are made up of chemicals based mostly on the element carbon Figure 4.1

3. 3 Carbon Chemistry Organic chemistry is the study of carbon compounds Carbon atoms can form diverse molecules by bonding to four other atoms Carbon compounds range from simple molecules to complex ones Carbon has four valence electrons and may form single, double, or triple.

4. 4 The bonding versatility of carbon allows it to form many diverse molecules, including carbon skeletons (a) Methane (b) Ethane (c) Ethene (ethylene) Molecular Formula Structural Formula Ball-and- Stick Model Space- Filling Model H H H H H H H H H H HH H H C C C CC CH 4 C2H6C2H6 C2H4C2H4 Name and Comments Figure 4.3 A-C

5. 5 The electron configuration of carbon gives it covalent compatibility with many different elements H O NC Hydrogen (bonds = 1) Oxygen (bonds = 2) Nitrogen (bonds = 3) Carbon (bonds = 4) Figure 4.4

6. 6 Carbon may bond to itself forming carbon chains Carbon chains form the skeletons of most organic molecules Carbon chains vary in length and shape H H H H H H H H H H H HHH H H H H H H H H H H H H H H H H HH HH HH HHH H HH HH H H H H H H H C C CCC CCCCCCC CCCCCCCC C C C C C C C C C C C C H H H H H H H (a) Length (b) Branching (c) Double bonds (d) Rings Ethane Propane n-Butane isobutane 1-Butene2-Butene Cyclohexane Benzene HH HHH Figure 4.5 A-D

7. 7 Hydrocarbons Hydrocarbons are molecules consisting of only carbon and hydrogen Hydrocarbons Are found in many of a cell’s organic molecules (a) A fat molecule (b) Mammalian adipose cells 100 µm Fat droplets (stained red) Figure 4.6 A, B

8. 8 Isomers Isomers are molecules with the same molecular formula but different structures and properties Three types of isomers are –Structural –Geometric –Enantiomers H H HH H H H H HH H H H HH H H H H H H H H H H H H H CO 2 H CH 3 NH 2 C CO 2 H H CH 3 NH 2 XX X X C CCCC C C C C C C C C C C (a) Structural isomers (b) Geometric isomers (c) Enantiomers H Figure 4.7 A-C

9. 9 Enantiomers Are important in the pharmaceutical industry L-Dopa (effective against Parkinson’s disease) D-Dopa (biologically inactive) Figure 4.8

10. 10 Functional Groups Functional groups are the parts of molecules involved in chemical reactions They are the chemically reactive groups of atoms within an organic molecule They give organic molecules distinctive chemical properties CH 3 OH HO O CH 3 OH Estradiol Testosterone Female lion Male lion Figure 4.9

11. 11 Seven functional groups are important in the chemistry of life –Hydroxyl –Carboxyl –Amino –Phosphate –Carbonyl –Methyl –Sulfhydryl

12. 12 Some important functional groups of organic compounds FUNCTIONAL GROUP STRUCTURE (may be written HO ) HYDROXYL CARBONYL CARBOXYL 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 –.) 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 The carbonyl group ( CO) consists of a carbon atom joined to an oxygen atom by a double bond. 

13. 13 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