1 / 11

ORGANIC CHEMISTRY

ORGANIC CHEMISTRY. PART III: ORGANIC REACTIONS. Substitution. Used to place a halogen onto an alkane Must use the halogen in diatomic form The products are always a halocarbon and hydro_______ acid. Needs ultraviolet light to activate the reaction. Addition.

lindaford
Download Presentation

ORGANIC CHEMISTRY

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. ORGANIC CHEMISTRY PART III: ORGANIC REACTIONS

  2. Substitution • Used to place a halogen onto an alkane • Must use the halogen in diatomic form • The products are always a halocarbon and hydro_______ acid. • Needs ultraviolet light to activate the reaction

  3. Addition • Takes place with unsaturated compounds which are usually more reactive that saturated compounds • Add a halogen across a double bond

  4. Polymerization • Making of polymers from monomers. • Monomers – individual units of a polymer. • Addition polymerization – alkenes or alkynes joining together to form a long chain saturated hydrocarbon. • Used to create plastics and rubber

  5. Condensation polymerization – monomers contain OH and/or NH2 groups • Results in two products, a polymer and water • Used to create nylon and polyester

  6. Dehydrate 2 primary alcohols and produce water and an ether CH3CH2CH2OH+CH3CH2CH2CH2OH→ (1- propanol) (1- butanol) HOH+CH3CH2CH2OCH2CH2CH2CH3 (water) (propyl butyl ether) Making Ethers

  7. Esterification • Alcohol + Acid = Water + Ester • Used in making perfumes and scents • Combination reaction which involves dehydration. • The alcohol becomes the alkyl group and the acid becomes the -oate

  8. Enzymes are used as catalysts and sugars are broken down to alcohols and carbon dioxide ZymaseC6H12O6 2 C2H5OH + 2 CO2 Glucose Ethanol Carbon dioxide Fermentation

  9. Hydrolysis of fats by a strong base (KOH or NaOH) Products are soap and glycerol Saponification

  10. Practical Application • Alkyl halides – used as solvents, cleaning agents, nonstick coatings (PTFE), refrigerants (CFCs) • Denatured alcohols (solvents, fuel) • Ethers – anesthetics for surgery • Amines – dyes, pesticides, plastics, tires • Aldehydes – preservatives, buttons, appliance and automotive parts, adhesives • Ketones – acetone, solvents for waxes, plastics, paints, glues • Organic acids – insects, foods, used to make esters • Esters – flavors, fragrances – foods, candles, perfumes, etc.

  11. Petroleum • Crude oil from the earth is made up of many of hydrocarbons • In order to separate it into many useful compounds, two processes are used • Cracking – use of high heat, to break long hydrocarbon chains into smaller ones • Fractional distillation – separation of hydrocarbons due to differences in boiling points

More Related