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Chapter 4 Functional Groups Chapter 5 Macromolecules

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1 Chapter 4 Functional Groups Chapter 5 Macromolecules
Biochemistry Chapter 4 Functional Groups Chapter 5 Macromolecules

2 Carbon—The Backbone of Biological Molecules
All living organisms Are made up of chemicals based mostly on carbon due to its bonding ability All life considered “carbon based life-forms”

3 Biochemistry Part 1 Chapter 4: Functional Groups

4 Chapter 4 Organic chemistry
the study of carbon compounds Organic compounds have carbon in them (& usually H) Exception: CO2 is considered INORGANIC Range from simple to big molecules

5 Formation of Bonds w/ Carbon
Carbon atoms forms diverse molecules b/c carbon has 4 valence electrons bind to to 4 other atoms can form 4 covalent bonds with itself or other atoms  very important in living things! Carbon has bonding versatility allows it to form many diverse molecules, including carbon skeletons (carbon “chains”)

6

7 The electron configuration of carbon
Gives it covalent compatibility with many different elements H O N C Hydrogen (valence = 1) Oxygen (valence = 2) Nitrogen (valence = 3) Carbon (valence = 4) Figure 4.4

8 Molecular Diversity Arising from Carbon Skeleton Variation
Carbon chains Form skeletons of most organic molecules Vary in length and shape Straight Branched Rings

9 Hydrocarbons Organic molecules consisting of only C and
Ex: petroleum; lipid ‘tails’ Found in many of cell’s organic molecules Ex: fat molecules Covalent bonding btw C-H nonpolar (hydrophoic) High energy storage

10 Example of a Hydrocarbon
(a) A fat molecule (b) Mammalian adipose cells 100 µm Fat droplets (stained red) Figure 4.6 A, B

11 ISOMERS Isomers same molecular formula, but different structure & properties Have same # of atoms arranged differently 3 types of isomers structural~ differ in covalent bonding arrangement geometric~ differ in spatial arrangement Arise from inflexibility of double C bond cis (same side) vs. trans (opposite sides) enantiomers~ mirror images of each other Ex: used in pharmacological industry

12 1 usually active; other inactive
Example of Isomers Straight vs. branched Cis vs. trans 1 usually active; other inactive Asymmetrical Carbon

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

14 Functional Groups Functional groups parts of organic molecules involved in chemical rxns (i.e.-chemically reactive groups) each functional group behaves in a consistent fashion from 1 organic molecule to the next # & arrangement of groups helps give molecules unique, distinctive chemical properties

15 7 functional groups important in chemistry of life
Hydroxyl Carbonyl Carboxyl Amino Sulfhydryl Phosphate Methyl

16 Functional Groups 1. Hydroxyl Group (-OH) H bonded to O
Attachments replace 1+ of H’s bonded to C skeleton of the hydrocarbon Each GROUP are HYDROPHILIC  increase organic molecule solubility in water 1. Hydroxyl Group (-OH) H bonded to O Make alcohols, sugars polar (b/c of oxygen electronegivity) soluble in water (attracts H20)

17 Functional Groups 2. Carbonyl Group (C=O) C double bond to O
Aldehyde (at the end of C skeleton) Ketone (INSIDE Carbon skeleton) Ex: Acetone, Propanal

18 Aldehyde **Think: all the way at the end! Ketone

19 Functional Groups cont’d
3. Carboxyl Group (-COOH) O double bonded to C to hydroxyl Carboxylic acids (organic acids) Covalent bond between O and H Polar Dissociation  H ion source (Acidic properties) **Think: Carboxyl has a hydroxyl!

20 Functional Groups cont’d
4. Amino Group (-NH2) N to 2 H atoms Makes Amines Acts as a base (+1) Also makes AMINO ACIDS Have both amino and carboxyl groups

21 Functional Groups cont’d
5. Sulfhydral Group (-SH) sulfur bonded to H Makes disulfide bridges 2 sulfhydral groups can interact to stabilize protein structure

22 Functional Groups cont’d
6. Phosphate Group (-OPO3-) Organic phosphates Forms phosphate ion Covalently attached by 1 of its O to the C skeleton Can transfer energy btw organic molecules Ex: ATP

23 Functional Groups cont’d
7. Methyl Group (-CH3) Usually not as reactive as other groups Used in gene expression

24 Male or Female!! Only one little itty bitty difference that separates the sexes


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