Organic Reactions Combustion hydrocarbons readily react with O 2.

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Presentation transcript:

Organic Reactions

Combustion hydrocarbons readily react with O 2

combustion complete combustion: sufficient O 2 leads to only 2 products: CO 2 & H 2 O C 3 H 8 (g) + 5O 2 (g)  3CO 2 (g) + 4H 2 O(g) incomplete combustion: insufficient O 2 leads to various products formed: C, CO, CO 2 & H 2 O C 3 H 8 (g) + 2O 2 (g)  3C(s) + 4H 2 O(g)

Substitution replace one or more H’s in hydrocarbon with something else

C 2 H 6 + Cl 2  C 2 H 5 Cl + HCl H  C  C  H + Cl  Cl  H  C  C  H + HCl H H Cl start with saturated hydrocarbon replace H atom with another atom or group 2 2 products

Addition open up multiple bond(s) to add new atoms (ex: halogens) Subtraction creating multiple bond(s) by losing atoms (ex: remove halogens from halocarbon)

H  C=C  H + Cl  Cl  H  C  C  H reverse rxn would be sutraction H Cl H add across double or triple bond start with unsaturated hydrocarbon 1product ony: 1 saturated product C 2 H 4 + Cl 2  C 2 H 4 Cl 2

Esterification formation of ester: organic acid + alcohol  ester + water

H H = O H H H H 2 O H  C  C  O  C  C  C  H H 2 O = O HH HH H H H +  1-propanol + OHH H  C  C  OH HO  C  C  C  H   ethanoic acid    propyl ethanoate  water

Saponification make soap: fat + base  glycerol + soap

HCCCHHCCCH  O  C  C 17 H 35 HH HH HH NaOH + fat + base   (triglyceride) = O = O = O

H  C  OH  C  OH  C  OH  H HH HH HH + Na  O  C  C 17 H 35 == = O O O glycerol + soap (1,2,3 propanetriol)

Fermentation sugars broken down into alcohol + CO 2

enzyme is needed to break down sugars into alcohol + CO 2 C 6 H 12 O 6  2C 2 H 5 OH + 2CO 2 zymase sugar ethanol carbon dioxide

What do protein in eggs, plastic in soda bottles, rubber in tires and teflon coating cookware have in common? polymersall are made up of giant molecules called polymers –poly means many –mers means parts

Polymers very large molecules consisting of many repeating structural units –analogy = chain consisting of many links masses can be > 1,000,000 amu monomer: small molecule from which polymer is made –starting material

Natural Polymers wool

silk

rubber

starch found in root plants corn starch

proteins

nucleic acids Nucleic acids are polymers formed by attaching monomers called nucleotides two nucleic acids: DNA & RNA nucleotides fall into two classes: purines & pyrimidines –purines: A & G –pyrimidines: T & C RNA has U instead of T

Synthetic Polymers plastics – polyethylene, PVC synthetic fibers – nylon, rayon, polyester rubber substitutes – polyurethane

Polymerization Reactions: chemical reactions that produce polymers revolutionized our everyday lives two reaction types: addition & condensation

1.addition polymerization 1.addition polymerization: - start with unsaturated monomers - all - all reactants used up 1 saturated product formed

C=C     H H H H H H H H H H        C  C  C  C  C  C        H H H H H H n n  ethene (monomer) polyethylene (polymer) repeating segment

Polyethylene Varieties milk bottles detergent bottles oil bottles bottle caps plastic grocery bags shrink-wrap films sandwich bags toys

Polyethylene Products #1: PETE or PET (Polyethylene Terephthalate) usually clear used for: soda bottles, water bottles, beer bottles, salad dressing containers, mouthwash bottles, and peanut butter containers known to allow bacteria to accumulate recycled into: tote bags, furniture, carpet, paneling, fiber, and polar fleece

Substituted Ethylenes H C=C H CH 3  H H H H H H H H  C  C  C  C  C  C  C  C  H  H  H  H  CH 3 indoor-outdoor carpet upholstery fabrics

Polyvinyl Chloride (PVC) H C=C H Cl  H H H H H H H H  C  C  C  C  C  C  C  C  H Cl H Cl H Cl H Cl phonograph records, garden hoses, pipes replace all H ’ s with Cl & you get Saran wrap

Teflon F F C=C F F n  F F F F F F  C  C  C  C  C  C  F F F F F F

2. Condensation Polymerization 2. Condensation Polymerization: –combine monomers containing 2 func groups –monomer has functional group at each end –loss of a small by-product, usually H 2 O

H H O  H H  O  C  C  O  H H H + H H  O  C  C  OH H H  H H H H H  O  C  C  O  C  C  O  H H H H H + H2OH2OH2OH2O

Nylon HO  C  C  C  C  C  C  OH = = O O + NH 2  C  C  C  C  C  C  NH 2  CCCCCCNCCCCCCNCCCCCCNCCCCCCN = = OO  H  H n + H2O+ H2O

Congratulations !!!! You ’ re now finished with the required curriculum required curriculum !