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Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4....

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Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons 13-7. Benzene 13-8. Hydrocarbon Groups 13-9. Functional Groups 13-11. Carbohydrates 13-12. Photosynthesis 13-13. Lipids 13-14. Proteins 13-15 Soil Nitrogen 13-16. Nucleic Acids 13-17. Origin of Life
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Page 1: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Chapter 13 Organic Chemistry

13-1. Carbon Bonds13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons13-7. Benzene 13-8. Hydrocarbon Groups13-9. Functional Groups 13-10. Polymers

13-11. Carbohydrates

13-12. Photosynthesis

13-13. Lipids

13-14. Proteins

13-15 Soil Nitrogen

13-16. Nucleic Acids

13-17. Origin of Life

Page 2: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Organic chemistry is the chemistry of carbon compounds; inorganic chemistry is the chemistry of compounds of all elements other than carbon.

The general properties of carbon compounds are:

1. Most carbon compounds are non-electrolytes.

2. The reaction rates of carbon compounds are usually slow.

3. Many carbon compounds oxidize slowly in air but rapidly if heated.

4. Most carbon compounds are unstable at high temperatures.

Page 3: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-3. Petroleum Products Fractional distillation

                                                                                               

Catalytic cracking Modern cracking uses zeolites as the

catalyst.

Page 4: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-3. Petroleum Products

Page 5: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-5. Isomers

Optical Isomers Structural Isomers

13-6. Unsaturated Hydrocarbons

Unsaturated compounds have double or triple carbon-carbon bonds and are more reactive than saturated compounds, which have only single carbon-carbon bonds (alkanes and similar compounds).

http://www.chembio.uoguelph.ca/educmat/chm19104/isomers/intro.htm

http://www.chembio.uoguelph.ca/educmat/chm19104/isomers/stereoisomers/index.htm

Page 6: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13.7 Benzene Aromatic compounds

Aliphatic compounds are organic compounds that do not contain benzene rings.

Page 7: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13.8 Hydrocarbon Groups

Alkanes or Hydrocarbons

Methane 1 carbon

Ethane 2 carbons

Propane 3 carbons

Butane 4 carbons

Pentane 5 carbons

Hexane 6 carbons

Heptane 7 carbons

Octane 8 carbons

Page 8: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Table 13.1

Page 9: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-9. Functional Groups

Alkenes

Ethene 2 carbons

Propene 3 carbons

Butene 4 carbons

Pentene 5 carbons

Hexene 6 carbons

Heptene 7 carbons

Octene 8 carbons

Alkynes

Acetylene 2 carbons

Propyne 3 carbons

Butyne 4 carbons

Pentyne 5 carbons

Hexyne 6 carbons

Heptyne 7 carbons

Octyne 9 carbons

Page 10: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Fig. 13.9, etc.

Acetylene gas welding and cutting.

Page 11: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Alcohols

Ethanol 2 carbons

Propanol 3 carbons

Butanol 4 carbons

Pentanol 5 carbons

Hexanole 6 carbons

Heptanol 7 carbons

Octanol 8 carbons

13-9. Functional Groups

Page 12: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Ethersoxygen in the middle

AldehydesDouble bond “O” with “H” on end

13-9. Functional Groups

Page 13: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

KetonesDouble bond “O” in middle

13-49 Functional Groups

Carboxylic AcidsDouble bond “O” with “OH”

Page 14: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

AminesNH2 on end

13-9. Functional Groups

EstersDouble bond “O” with “O” both in middle

Page 15: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Table 13.2

Page 16: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-10 Polymers

A polymer is a long chain of simple molecules (monomers) linked together. Polymers that contain the vinyl group are classed as vinyls. Some examples of polymers include Styrofoam, Teflon, Orlon, and Plexiglas (or Lucite). Plexiglas is thermoplastic, meaning it softens and can be shaped when heated but becomes rigid again on cooling..

Page 17: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Polymerization-the making of plastics

Vinyl

13-3. Petroleum Products

Page 18: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Table 13.3

Page 19: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-10 Polymers

.A copolymer is a polymer that consists of two different monomers. Dynel and Saran Wrap are examples. Certain monomers that contain two double bonds in each molecule form flexible, elastic polymers called elastomers; rubber and neoprene are examples. Polyamides and polyesters are polymers produced by chemical reactions rather than by the polymerization of monomers.

Page 20: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-10 Polymers

.Teflon is polymer with a strong bond between carbon and fluorine atoms. It is used as a no-stick surface in cookware.

Page 21: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-11. Carbohydrates

                    

          

          

          

           

          

           

          

           

          

           

          

           

          

           

D-Allose D-Altrose D-Glucose D-Mannose D-Gulose D-Idose D-Galactose D-Talose

                                                                       

D-Glucose(an aldose)

α-D-Glucose β-D-Glucose

                    

    

                    

    

                              

      

β-D-Glucose(chair form)

Page 22: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

                                                                                                

                                                  

Sucrose Lactose Maltose

13.11 Polysaccharides

Amylopectin

Page 23: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Cellulose in wood is extracted and converted to paper at this plant in Maine. Microorganisms in the stomachs of cows help them digest cellulose in plants.

13.11 Polysaccharides

Page 24: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13.12 Photosynthesis

Page 25: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13.12 Photosynthesis

Page 26: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-13. Lipids

Saturated and Unsaturated Fatty Acid

Soap Molecule with Polar head and non-polar tail

Page 27: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-13. Lipids

Page 28: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-14. Proteins The polypeptide chain forms a backbone structure in proteins:

                                                     

                                                 

On first inspection, this structure appears to be connected entirely by single C-C or C-N bonds. It should therefore be as flexible as a simple hydrocarbon chain. Note that flexing in a covalent structure does not occur by bending bonds, and the normal tetrahedral or trigonal planar bond angles are maintained. Instead, different shapes are obtained by torsional rotation about the axis of the bonds:

                                    

                                            

                                                                                                     

                                                  

                                                  

Page 29: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-15 Soil Nitrogen

Page 30: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-16. Nucleic Acids

. Chromosomes consist of DNA molecules. Changes in the sequence of the bases in a DNA molecule can result in a mutation.

Page 31: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-17. Origin of Life

Page 32: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

2001 Space Odyssey

HAL 9000Where did Clarke and Kuberick

get the name HAL?

IBM

IBM thought Hardware would be King! Net worth in 2013 $112.5 billion.

Who really became King?

Bill Gates software MS DOS! Net worth $72.6 billion in 2013

Microsoft Net worth $290 billion in 2013

.

Page 33: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-17. Origin of Life

Page 34: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

13-16. Nucleic Acids

. Chromosomes consist of DNA molecules. Changes in the sequence of the bases in a DNA molecule can result in a mutation.

Page 35: Chapter 13 Organic Chemistry 13-1. Carbon Bonds 13-2. Alkanes 13-3. Petroleum Products 13-4. Structural Formulas 13-5. Isomers 13-6. Unsaturated Hydrocarbons.

Intelligent Designhttp://www.youtube.com/watch?v=1CwL7xXUriE#t=23

DNAMoon same size as the sun to usAtmosphere Magnetic fieldJust right size for the right gravityJust the right distance from the sunTitius -Bode Law-planetary distances from sun have a patternDark energy and matterPatterns in electron energy levelsThe brain-greatest brain authority says we know nothingThe eye-seeing only colorsOnly 4 basic forces?? What about Intelligence?What are the 4 forces and where do they come from?There is no evidence that one species has changed into anotherTunneling affect of electronsNot enough time for man to evolve by chance (14 billion years)Paranormal evidence


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