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Carbon and the Molecular Diversity of Life

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1 Carbon and the Molecular Diversity of Life
4 Carbon and the Molecular Diversity of Life Lecture Presentation by Nicole Tunbridge and Kathleen Fitzpatrick

2 Carbon: The Backbone of Life
Living organisms consist mostly of carbon-based compounds Carbon is unparalleled in its ability to form large, complex, and varied molecules Proteins, DNA, carbohydrates, and other molecules that distinguish living matter are all composed of carbon compounds

3 Carbon can bond to four other atoms or
Figure 4.1a Figure 4.1a What properties make carbon the basis of all life? (part 1: carbon atom) Carbon can bond to four other atoms or groups of atoms, making a large variety of molecules possible.

4 Concept 4.1: Organic chemistry is the study of carbon compounds
Organic chemistry is the study of compounds that contain carbon With four valence electrons, carbon can form four covalent bonds with a variety of atoms This ability makes large, complex molecules possible

5 Molecular Formula Structural Formula Space-Filling Model Molecule
Figure 4.3 Molecular Formula Structural Formula Space-Filling Model Molecule Ball-and-Stick Model (a) Methane CH4 (b) Ethane C2H6 Figure 4.3 The shapes of three simple organic molecules (c) Ethene (ethylene) C2H4

6 Carbon atoms can partner with atoms other than hydrogen; for example:
Carbon dioxide: CO2 Urea: CO(NH2)2

7 Figure 4.UN02 Urea Figure 4.UN02 In-text figure, urea, p. 60

8 Molecular Diversity Arising from Variation in Carbon Skeletons
Carbon chains form the skeletons of most organic molecules Carbon chains vary in length and shape

9 2-Methylpropane (isobutane)
Figure 4.5 (a) Length (c) Double bond position Ethane Propane 1-Butene 2-Butene (b) Branching (d) Presence of rings Figure 4.5 Four ways that carbon skeletons can vary Butane 2-Methylpropane (isobutane) Cyclohexane Benzene

10 Hydrocarbons Hydrocarbons are organic molecules consisting of only carbon and hydrogen Many organic molecules, such as fats, have hydrocarbon components Hydrocarbons can undergo reactions that release a large amount of energy

11 Isomers Isomers are compounds with the same molecular formula but different structures and properties Structural isomers have different covalent arrangements of their atoms Cis-trans isomers have the same covalent bonds but differ in spatial arrangements Enantiomers are isomers that are mirror images of each other

12 (a) Structural isomers
Figure 4.7 (a) Structural isomers Pentane 2-methyl butane (b) Cis-trans isomers cis isomer: The two Xs are on the same side. trans isomer: The two Xs are on opposite sides. (c) Enantiomers Figure 4.7 Three types of isomers, compounds with the same molecular formula but different structures CO2H CO2H C C H NH2 NH2 H CH3 CH3 L isomer D isomer

13 Enantiomers are important in the pharmaceutical industry
Two enantiomers of a drug may have different effects Usually only one isomer is biologically active Differing effects of enantiomers demonstrate that organisms are sensitive to even subtle variations in molecules

14 Effective Enantiomer Ineffective Enantiomer Drug Effects Reduces
Figure 4.8 Effective Enantiomer Ineffective Enantiomer Drug Effects Reduces inflammation and pain Ibuprofen S-Ibuprofen R-Ibuprofen Relaxes bronchial (airway) muscles, improving airflow in asthma patients Figure 4.8 The pharmacological importance of enantiomers Albuterol R-AIbuterol S-AIbuterol

15 Functional groups are the components of organic molecules that are most commonly involved in chemical reactions The number and arrangement of functional groups give each molecule its unique properties

16 The seven functional groups that are most important in the chemistry of life
Hydroxyl group Carbonyl group Carboxyl group Amino group Sulfhydryl group Phosphate group Methyl group

17 Figure 4.9 Some biologically important chemical groups
Compound Name Examples Hydroxyl group (—OH) Alcohol Ethanol Carbonyl group ( C=O) Ketone Aldehyde Acetone Propanal Carboxyl group (—COOH) Carboxylic acid, or organic acid Acetic acid Amino group (—NH2) Amine Glycine Sulfhydryl group (—SH) Thiol Cysteine Figure 4.9 Some biologically important chemical groups Phosphate group (—OPO32−) Organic phosphate Glycerol phosphate Methyl group (—CH3) Methylated compound 5-Methyl cytosine

18 ATP: An Important Source of Energy for Cellular Processes
An important organic phosphate is adenosine triphosphate (ATP) ATP consists of an organic molecule called adenosine attached to a string of three phosphate groups ATP stores the potential to react with water, a reaction that releases energy to be used by the cell

19 Figure 4.UN04 Adenosine Figure 4.UN04 In-text figure, ATP phosphate chain, p. 64

20 Reacts with H2O P P P Adenosine P P P Adenosine Energy ATP Inorganic
Figure 4.UN05 Reacts with H2O P P P Adenosine P P P Adenosine Energy i ATP Inorganic phosphate ADP Figure 4.UN05 In-text figure, ATP to ADP reaction, p. 64


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