0. Classes of Organic Compounds
ORGANIC CHEMISTRY
Classes of Organic Compounds

1. Classification of Hydrocarbons
1. Aromatic Hydrocarbons-contain one or
more benzene rings
2. Aliphatic Hydrocarbons - all other
hydrocarbons

2. Aliphatic Hydrocarbons
Carbon atoms can be bonded in straight chains, branched chains, or rings.
Chains may contain single, double, or triple bonds.
A saturated compound contains only single bond between carbons. These are alkanes.

3. ALKANES Simplest hydrocarbon
Each differs from the next by a -CH2- group.
Compounds whose structures differ from each other by a specific structural unit is called a homologous series.

4. ALKANES Simplest alkane is methane. CH4
General formula of alkane is CnH2n+2
All end in -ane
Soluble in nonpolar solvents,
C to C bonds have sp3 hybridization.

5. Hydrocarbon Prefixes

6. ALKANES
When a hydrogen along with its associated electrons is removed from a hydrocarbon molecule, a radical is left.
CH3 is a radical. It is named methyl.
Radicals end in -yl.
Alkanes form alkyl groups.

7. Branched Chain Alkanes
1. Find longest continuous chain or parent chain.
2. Add the name of the branches (substituents) attached in alphabetical order using prefixes.
3. Number Carbon atoms in parent
4. Insert position # of each substituent group
5. Punctuate name - separate position # with hyphens, more than one # is separated by commas.

8. Cycloalkanes Alkane rings General formula is CnH2n
Example cyclopentane C5H10

9. Isomers
Isomerism is the existence of two or more substances with the same molecular formula, but different molecular structures.
Important because structure determines properties and function.
There are two main types of isomers.

10. Structural Isomers

11. Structural Isomers Also called constitutional isomers.
Atoms are bonded in different arrangements--thus different properties.

13. Longer chains have higher boiling points (BP) and melting points (MP)
Having branches on the chain serves to lower the BP but it raises the melting point.

14. Stereoisomers
All atoms are bonded in the same order but are arranged differently in space.
There are two types:
a. Geometric isomers
b. Optical isomers

15. Geometric Isomers
Structural isomers have a different arrangement of groups around a double bond.
In alkenes with double bonds, the carbon is locked in place and cannot rotate freely as it could in alkanes with single bonds. Pi bonds

16. Geometric isomers

17. Optical Isomers
Optical Isomerism (Chiralty) occurs when there is an asymmetric carbon (C has 4 different atoms or groups attached)

19. Chiral Molecules

20. Chirality is important in drugs and enzyme-catalyyzed rxns
Chirality is important in drugs and enzyme-catalyyzed rxns. Only L-form of ascorbic acid functions as vitamin C.

22. Geometric Isomers

23. Properties and Uses of Alkanes
1. C-H bonds are nonpolar
2. Strength of London dispersion forces increases as mass increases--# of C determines state of matter.
3. Longer the chain, higher the boiling point.

24. Properties and uses of alkanes
4. Alkanes less reactive than other hydrocarbons due to stability of single covalent bonds.
5. Most important rxn is combustion.

25. Fractional Distillation
Gasoline is a component of fossil fuel. Is can be extracted by fractional distillation.

26. Combustion
Straight-chain alkanes ignite more spontaneously than branched chains but cause knocking in autos.
Octane rating is a measure of burning efficiency and antiknock properties.
2,2,4-trimethyl pentane (isooctane) resists knocking

27. C8H18
2,2,4-trimethylpentane octane

28. Unsaturated Hydrocarbons
Contain double and triple carbon to carbon bonds.
Include Alkenes and Alkynes

29. ALKENES Olefin is another name. Contain double bonds.
General formula CnH2n
Double bond is shorter than a single bond and it is also stronger and more reactive.
Double C bonds have sp2 hybridization.

30. Naming Alkenes End in -ene.
The double bond location takes precedence in naming.
If there is more than one double bond, the location is numbered and a prefix is used
2 = adiene 3 = atriene

31. Alkenes are numbered so that the lowest position number is assigned to the first carbon atom to which the double bond is attached.

32. 1,4-pentadiene

33. Ethene #1 organic chemical in industry Product of petroleum refining
Makes plastics and
synthetics

34. ALKYNES Contain triple bonds. General formula is CnH2n-2 End in -yne
Ethyne or acetylene

35. Naming Alkynes
The numbering system follows the same pattern used for naming alkenes.
4,4-dimethyl-2-pentyne

36. If a compound has both double and triple bonds, the double bonds take precedencein numbering.
The double bond is given the lowest number and named first.

37. Benzene Ring
Kekule’s snake

38. AROMATIC HYDROCARBONS
Contain Benzene ring
Most have distinctive odors.
Thousands of compounds are derived from benzene.

40. Ways to diagram benzene
Important in making plastics and fibers

41. Naphthalene
2 benzene rings

42. Phenyl Radical

43. Methyl Benzene or Toluene
improves quality of gasoline
used in production of
explosives
TNT

44. Functional Groups
A substituent group that is not made up of only carbon and hydrogen is a functional group.
-OH is hydroxide