1. Chapter 22 Organic and Biological Chemistry

2. Organic Chemistry The chemistry of carbon compounds.
Carbon has the ability to form long chains.
Without this property, large biomolecules such as proteins, lipids, carbohydrates, and nucleic acids could not form.

3. Hydrocarbons Four basic types: Alkanes Alkenes Alkynes
Aromatic hydrocarbons

4. Alkanes Only single bonds. Saturated hydrocarbons.
“Saturated” with hydrogens.

5. Formulas Lewis structures of alkanes look like this.
Also called structural formulas.
Often not convenient, though…

6. Formulas
…so more often condensed formulas are used.

7. Properties of Alkanes Only van der Waals force: London force.
Boiling point increases with length of chain.

8. Isomers
Have same molecular formulas, but atoms are bonded in different order.

9. Organic Nomenclature Three parts to a compound name:
Base: Tells how many carbons are in the longest continuous chain.

10. Organic Nomenclature Three parts to a compound name:
Base: Tells how many carbons are in the longest continuous chain.
Suffix: Tells what type of compound it is.

11. Organic Nomenclature Three parts to a compound name:
Base: Tells how many carbons are in the longest continuous chain.
Suffix: Tells what type of compound it is.
Prefix: Tells what groups are attached to chain.

12. Bases(Parent)

13. Branches

14. To Name a Compound… Find the longest chain in the molecule(base).
Number the chain from the end nearest the first substituent(branch) encountered.
List the branches as a prefix along with the number(s) of the carbon(s) to which they are attached.

15. To Name a Compound…
4. If there is more than one type of branch in the molecule, list them alphabetically. Use prefixes,di-, tri-, to indicate multiple branches.

16. Example 1: 2,2-dimethylpentane
The parent chain is indicated by the ROOT of the name - “pentane”. This means there are 5 carbons in the parent chain. 1 2 3 4 5
“dimethyl” tells us that there are TWO methyl branches on the parent chain. A methyl branch is made of a single carbon atom.
“2,2-” tell us that BOTH methyl branches are on the second carbon atom in the parent chain.

17. Example 2: 3-ethyl-2,4-dimethylheptane1 2 3 4 5 7 6
The parent chain is indicated by the ROOT of the name - “heptane”. This means there are 7 carbons in the parent chain.
“2,4-dimethyl” tells us there are TWO methyl branches on the parent chain, at carbons #2 and #4.
“3-ethyl-” tell us there is an ethyl branch (2-carbon branch) on carbon #3 of the parent chain.

18. Example 3: 2,3,3-trimethyl-4-propyloctane
The parent chain is indicated by the ROOT of the name - “octane”. This means there are 8 carbons in the parent chain. 1 2 3 4 5 7 6 8
“2,3,3-trimethyl” tells us there are THREE methyl branches - one on carbon #2 and two on carbon #3.
“4-propyl-” tell us there is a propyl branch (3-carbon branch) on carbon #4 of the parent chain. 1 2 3 4 5 7 6 8

19. Example 4: Name the molecules shown!
parent chain has 5 carbons - “pentane”
two methyl branches - start counting from the right - #2 and #3
2,3-dimethylpentane
parent chain has 8 carbons - “octane”
two methyl branches - start counting from the left - #3 and #4
one ethyl branch - #5
name branches alphabetically 5
5-ethyl-
3,4-dimethyl 4 3
octane

20. Cycloalkanes Carbon can also form ringed structures.
Five- and six-membered rings are most stable.
Can take on conformation in which angles are very close to tetrahedral angle.
Smaller rings are quite strained.

21. Alkenes Contain at least one carbon–carbon double bond. Unsaturated.
Have fewer than maximum number of hydrogens.

22. Structure of Alkenes
This creates geometric isomers, which differ from each other in the spatial arrangement of groups about the double bond.

23. Nomenclature of Alkenes
Chain numbered so double bond gets smallest possible number.
cis- alkenes have carbons in chain on same side of molecule.
trans- alkenes have carbons in chain on opposite side of molecule.

24. Alkynes Contain at least one carbon–carbon triple bond.
Carbons in triple bond sp-hybridized and have linear geometry.
Also unsaturated.

25. Nomenclature of Alkynes
4-methyl-2-pentyne
Analogous to naming of alkenes.
Suffix is -yne rather than –ene.

26. Aromatic Hydrocarbons
Cyclic hydrocarbons.
Molecule is planar.
Many aromatic hydrocarbons are known by their common names.

27. Structure of Aromatic Compounds
Two substituents on a benzene ring could have three possible relationships
ortho-: On adjacent carbons.
meta-: One carbon between them.
para-: On opposite sides of ring.

28. Functional Groups
Term used to refer to parts of organic molecules where reactions tend to occur.

29. Alcohols Contain one or more hydroxyl groups, —OH
Named from parent hydrocarbon; suffix changed to -ol and number designates carbon to which hydroxyl is attached.

30. Ethers Tend to be quite unreactive.
Therefore, they are good polar solvents.

31. Carbonyl Compounds Contain C—O double bond.
Include many classes of compounds.

32. Aldehydes
At least one hydrogen attached to carbonyl carbon.

33. Ketones
Two carbons bonded to carbonyl carbon.

34. Carboxylic Acids CH3COOH Have hydroxyl group bonded to carbonyl group.
Tart tasting.
Carboxylic acids are weak acids.
Naming:
_____oic acid
CH3COOH

35. Carboxylic Acids

36. Esters Products of reaction between carboxylic acids and alcohols.
Found in many fruits and perfumes.
butanoate

37. Amines
Organic bases.
Generally have strong, unpleasant odors.

38. Amides Formed by reaction of carboxylic acids with amines.
This is the reaction that occurs between amino acids