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Christian Brothers High School Department of Chemistry

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Title: Christian Brothers High School Department of Chemistry


1
Christian BrothersHigh SchoolDepartment of
Chemistry
  • Organic Chemistry II

2
Organic Reactions
  • Much slower than inorganic reactions
  • Organic compounds can be toxic, but effects are
    usually cumulative, i.,e., there must be
    long-term exposure
  • Substitution
  • Addition
  • Formation of radicals and functional groups

3
Organic ChemistrySubstitution Reactions I
  • Knock off one or more hydrogens
  • Substitute another radical or an oxygen, halogen,
    sulfur, etc
  • Methane subst. 1 Cl for H Chloromethane
  • Subst. One more Cl for H dichloromethane or
    methylene chloride
  • Subst. One more Cl for H trichloromethane
    or chloroform
  • Subst. One more Cl for H tetrachloromethane or
    carbon tetrachloride

4
Organic ChemistryFormation of Free Radicals
  • Whenever a hydrogen atom is knocked off
  • Formation of a free radical
  • Always uses the yl suffix to indicate the
    radical
  • Functional group radicals also use the yl suffix
  • In generic formulae use R ROH means any
    alcohol
  • Bonds with other molecules and radicals to form
    new compounds
  • Examples methyl- CH3 ethyl- C2H5 propyl-
    C3H7 butyl- C4H9

5
Organic ChemistryFunctional Groups
  • Way of organizing different classes of compounds
  • Identify by structure
  • -OH hydroxyl group Alcohols
  • -OOH carboxyl group Organic Acids

6
Organic ChemistryAlcohols
  • Generic formula ROH
  • Characterized by the hydroxyl group -OH
  • Industrial solvent, cleaner, intermediary in
    reactions, beverages, miscible in water
  • Properties of alcohols are determined by where
    the hydroxyl groups attached
  • Primary alcohol- hydroxyl group on the end
  • Secondary alcohol- hydroxyl group attached to a
    carbon which is attached to one hydrogen
  • Tertiary alcohols- hydroxyl group attached to a
    carbon which is in the middle of the chain

7
Organic ChemistryOrganic Acids
  • Also known as carboxylic acids
  • Characterized by the carboxyl group OOH
  • Examples Acetic Acid CH3COOH
  • A 3 aqueous solution of acetic acid is vinegar
  • Butyric acid 4 carbons is produced by the
    spoiling of milk
  • Longer chain acids (primarily C18 with one or
    more double bonds are called polyunsaturated
    fatty acids)

8
Organic ChemistryOrganic Bases
  • Organic bases are known as amines
  • Primary amines have radicals substituted for the
    hydrogens on the ammonia molecule
  • Methylamine 1 methyl group
  • Dimethylamine 2 methyl groups
  • Triethylamine 3 ethyl groups
  • Other amines have the nitro group (NH2)
    substituted on other radicals

9
Organic ChemistryOther Functional Groups
  • Aldehydes and Ketones both contain the carbonyl
    group -CO
  • Aldehydes have the group attached to a hydrogen
    at the end of a chain H-CO
  • Ketones have the group attached to two carbons
    (See board)
  • Ethers R-O-R
  • Diethyl ether once used as a surgical anesthetic

10
Organic ChemistrySugars/Carbohydrates
  • Energy source in animal metabolism
  • Always end in ose
  • Simple sugars
  • Fructose
  • Glucose
  • Sucrose
  • Lactose
  • Complex Carbohydrates
  • Increasing stacking of rings
  • Long stacks of rings
  • Cellulose (plant fiber)
  • Wood

11
Organic ChemistryProteins
  • Enzymes
  • Structural Building Blocks
  • Amino Acids
  • Peptide backbone
  • Biomacromolecules (DNA)

12
Organic ChemistryPlastics (polymers)
  • Built from simple compounds (monomers)
  • Ethylene initiator polyethylene
  • Propylene initiator polypropylene
  • Butylene initiator polybutylene
  • Styrene initiator polystyrene
  • Vinyl chloride initiator polyvinyl
    chloride
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