1. Carbon and the Molecular Diversity of Life Chapter 4

2. CARBON Carbon is has ability to form large and complex, molecules Aspirin molecular formula?A triglyceride

3. Organic chemistry is study of carbon compounds EthanolHemoglobin

4. (Wohler 1828)  organic molecules can be synthesized from inorganic Don’t need a kidney to make urea!

5. Water vapor H2H2 “Atmosphere” Electrode Condenser Cold water Cooled water containing organic molecules Sample contains amino acids, hydrocarbons primitive sea conditions CH 4 Stanley Miller 1953 Organic molecules can arise spontaneously (abiotic synthesis) sparks

6. Miller Evidence for evolution Physical/natural laws govern all natural phenomena New Scientist – Stanley Miller’s exp

7. Carbon forms diverse molecules by bonding to 4 other atoms usually H, O, N Name Molecular Formula Structural Formula Ball-and-Stick Model Space-Filling Model (a) Methane (b) Ethane (c) Ethene (ethylene)

8. Molecular Diversity Arises from Carbon Chains Carbon chains form organic molecules – Why are these called “hydrocarbons”? EthanePropane 1-Butene2-Butene (c) Double bonds (d) Rings CyclohexaneBenzene Butane2-Methylpropane (commonly called isobutane) (b) Branching (a) Length

9. Hydrocarbons hydrophobic undergo reactions that release large amount of energy (ex. Fossil fuels) Ex. fats C 3 H 8 + 5 O 2 → 4 H 2 O + 3 CO 2 + Energy

10. Hydrocarbon: Fat is a fuel reserve in animals A triglyceride = why?

11. Isomers same molecular formula, but different atom bonding Structural isomers

12. Stereoisomer are “handed” Thalidomide, given for morning sickness in Europe in late 1950s. Sedative. Found to be teratogen Was found in some animals that only the S stereoisomer is teratogenic – but turns out they both are.

13. Functional groups are key to function of biological molecules Estradiol Testosterone Both steriods, both have 4 fused rings, note functional groups

14. The 7 functional groups most important in life: 1. Hydroxyl group OH

15. 2. Carbonyl group C=O

16. 3. Carboxyl group -COOH Acetic acid Acetate ion

17. 4. Amino group -NH2 STRUCTURE EXAMPLE NAME OF COMPOUND FUNCTIONAL PROPERTIES Amino Because it also has a carboxyl group, glycine is both an amine and a carboxylic acid; compounds with both groups are called amino acids. Amines Acts as a base; can pick up an H + from the surrounding solution (water, in living organisms). Ionized, with a charge of 1+, under cellular conditions. (ionized)(nonionized) Glycine

18. 5. Sulfhydryl group -SH Cysteine Cysteine is an important sulfur-containing amino acid. Thiols Two sulfhydryl groups can react, forming a covalent bond. This “cross-linking” helps stabilize protein structure. Cross-linking of cysteines in hair proteins maintains the curliness or straightness of hair. Straight hair can be “permanently” curled by shaping it around curlers, then breaking and re-forming the cross-linking bonds.

19. 6. Phosphate group -PO 4 STRUCTU RE EXAMPL E NAME OF COMPOU ND FUNCTION AL PROPERTI ES Phosphate In addition to taking part in many important chemical reactions in cells, glycerol phosphate provides the backbone for phospholipids, the most prevalent molecules in cell membranes. Glycerol phosphate Organic phosphates Contributes negative charge to the molecule of which it is a part (2– when at the end of a molecule; 1– when located internally in a chain of phosphates). Has the potential to react with water, releasing energy.

20. 7. Methyl group -CH 3 STRUCTURE EXAMPLE Methyl 5-Methyl cytidine is a component of DNA that has been modified by addition of the methyl group. 5-Methyl cytidine Addition of a methyl group to DNA, or to molecules bound to DNA, affects expression of genes. Arrangement of methyl groups in male and female sex hormones affects their shape and function.

21. ATP: Energy for Cellular Processes adenosine attached to a string of 3 phosphates

22. 1 phosphate split off to form ADP + energy