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Organic Chemistry

Organic Chemistry. Topic 11. What is Organic Chemistry?. The study of carbon and most carbon compounds “The chemistry of life” … but includes far more compounds than those made by living things. Bonding of Carbon Atoms.

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Organic Chemistry

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  1. Organic Chemistry Topic 11

  2. What is Organic Chemistry? • The study of carbon and most carbon compounds • “The chemistry of life” • … but includes far more compounds than those made by living things.

  3. Bonding of Carbon Atoms • Carbon can form so many compounds because carbon atoms easily form covalent bonds with other carbon atoms • Can be single, double, or triple covalent bonds

  4. Bonding of Carbon Atoms • Lewis Dot Diagram of Carbon in ground state • Lewis dot diagram of bonded carbon atom • Enables four covalent bonds • Tetrahedral shape • Angles are actually 109.50

  5. Some Terminology • Organic compounds containing only single bonds are said to be saturated. • Organic compounds containing one or more double or triple bonds are called unsaturated compounds.

  6. More Terminology • Hydrocarbons - organic compounds that contain only hydrogen and carbon atoms • Homologous series - group of related compounds in which each member differs from the one before by one additional unit. • Alkanes • Alkenes • Alkynes

  7. Chemistry Humor • According to a chemist, why is the world so diverse? • Because it's made up of alkynes of people.

  8. Alkanes • All single bonds between carbon atoms • Therefore, all saturated. • As the number of carbon atoms in this homologous series increases, so does the boiling point • Names end with “-ane”

  9. Alkanes • Methane - Natural gas • Ethane - Also natural gas • Propane - outdoor grills/home heating • Butane - lighters • Pentane, Hexane, Heptane, Octane, Nonane, Decane - all found in gasoline • Candle wax - 20 or more carbon atoms • Road Tar - 40 or more carbon atoms

  10. General Formula For Alkanes • Each successive carbon adds two more hydrogen atoms • Let’s develop a general formula for alkanes… • CnH2n+2

  11. Alkenes • Each member of alkene series contains one double covalent bond • Names are same as for alkanes, except change ending to “-ene”. • Ethene - (common name “ethylene”) • Unsaturated

  12. Alkenes • Let’s develop a general formula for “alkenes”…. • CnH2n

  13. Alkynes • Contain one triple bond between carbon atoms • Names are same as for alkanes, except change ending to “-yne”. • Ethyne (common name “acetylene” - used in welding torches)

  14. Alkynes • Let’s develop a general formula for alkynes • CnH2n-2 • Pull out Reference Tables… • Table P - Organic Prefixes • Table Q - homologous series & general formulas

  15. Homework • Review Book Page 197 #1-18.

  16. Let’s Keep some terms straight… • Molecular formula - represents the actual atoms in a molecule • Reminder - empirical formula is the simplest integer ratio in which atoms combine in a compound. • Structural Formula - attempts to show the kinds and numbers of atoms, but also the bonding patterns and approximate shapes • Condensed structural formulas

  17. Let’s Keep some terms straight… • Ball-and-stick model • Space-filling model (very similar to “molecular shape” model)

  18. Isomers • Get a model kit and build a ball-and-stick model of butane. • How many carbons and hydrogen did you need? • Use the same number of carbons and hydrogens, but build something different than the butane you built above.

  19. Isomers • Starting with butane there’s more than one way to combine the carbon and hydrogen atoms. • When a molecular formula can be represented by more than one structural arrangement, the compounds are called isomers of one another.

  20. Isomers • Even though they have the same molecular formula, isomers have different chemical and physical properties. • Different boiling points • Different reactivities • As the number of carbon atoms increases, so does the number of possible isomers.

  21. Naming Organic Compounds • When carbon atoms in one continuous chain, called a “straight chain” hydrocarbon • Also called “normal form” • The letter “n-” precedes the name of straight chain hydrocarbons

  22. Naming Organic Compounds • Compounds with branched chains must be given different names because they have different chemical and physical properties. • Naming rules are governed by IUPAC (International Union of Pure and Applied Chemistry)

  23. Naming Organic Compounds • Step 1 - Find the longest continuous chain of carbon atoms • The compound will be named based on its longest chain. • For example, if the longest chain is 6, then the compound will be named as a hexane.

  24. Naming Organic Compounds • Step 2 - Identify attached Alkyl Groups • An alkyl group contains one less hydrogen than an alkane with the same number of carbon atoms • Step 3 - Assign numbers to the carbon atoms in the longest chain. • They must be numbered from the end that will give the lowest number for the attached group.

  25. Naming Organic Compounds • Step 4 - Name the compound by stating the location of the attached chain, the alkyl group, then the main branch name

  26. Naming Organic Compounds • Some additional naming info… • If there is more than one of the same type of group attached to the parent chain, then a prefix is used • di- means two; tri- means three; tetra- means four • Commas are used to indicate the specific carbon to which each group is attached

  27. Naming Organic Compounds • Worksheet - Isomers of octane • Worksheet 25-4 Apply “A Compound Problem”

  28. Functional Groups • Functional Groups - are atoms or groups of atoms that replace hydrogen in a hydrocarbon, and give the compound distinctive chemical and physical properties.

  29. Organic Acids • Organic Acids are a homologous series • Functional group is carboxyl group (-COOH) • Name comes from corresponding hydrocarbon, but replace ending “-e” with “-oic acid” • Ethanoic acid (common name “acetic acid”, which is found in vinegar)

  30. Organic Acids • Most organic compounds are nonelectrolytes, but organic acids are weak electrolytes. • Reference Table R

  31. Alcohols • Alcohols - organic compounds where one hydrogen of a hydrocarbon is replaced by an -OH group (called a hydroxyl group) • The -OH group resembles the hydroxide ion, but it isn’t the same. It doesn’t form hydroxide ion in water. • Therefore, alcohols are nonelectrolytes

  32. Alcohols • The hydroxyl group is polar, though, which allows alcohols to dissolve in water. • Name by changing corresponding alkane ending “-e” to “-ol”

  33. Esters • Esters are organic compounds whose type formula is R-CO-ORI • Part comes from an organic acid, and the RI part comes from an alcohol • Esters have strong, fragrant odors.

  34. Esterification • Esterification - The organic reaction between an organic acid and an alcohol to produce an ester plus water. • Esters are named by using the alkyl name of the alcohol followed by the acid group modified to end in “-oate”.

  35. Esterification • Esterification Lab

  36. More About Alcohols • There are several different types of alcohols • Type depends on number of hydroxyl groups • Type depends on the position of each hydroxyl group on the chain

  37. Alcohols • Alcohols are primary, secondary, or tertiary based on whether the hydroxyl group is attached to a primary, secondary, or tertiary carbon atom. • Primary carbon - attached to only one other carbon atom • Secondary Carbon - attached to two other carbon atoms • Tertiary Carbon - attached to three other carbon atoms

  38. Alcohols • Primary Alcohol - has a hydroxyl group attached to primary carbon • Secondary Alcohol - hydroxyl group attached to secondary carbon • Tertiary Alcohol - hydroxy group attached to tertiary alcohol

  39. Alcohols • Monohydroxy alcohols - have one hydroxyl group • Dihydroxy alcohols - two hydroxyl groups • 1,2 ethanediol • Trihydroxy Alcohols- three hydroxyl groups • 1,2,3 propanetriol

  40. Some Practice • Page 204 #34,35, 39, 41, 42, 43,45

  41. Organic Halides (“Halocarbons”) • When a halogen (F, Cl, Br, or I) replaces a hydrogen on an alkane, the compound is called an organic halide (or halocarbon). • The functional group is the attached halogen. • Named by citing the location of the halogen attached to the chain.

  42. Ethers • Series of organic compounds in which two carbon chains are joined together by an oxygen atom bonded between two carbon atoms. • Named using alkyl group names followed by “ether”.

  43. Worksheet 26-1 Apply • Halocarbon, Alcohol, or Ether?

  44. Amines • Amines are formed when one of the hydrogens of ammonia is replaced by an alkyl group. • Named by taking the alkane name and change the ending “-e” to “-amine”, and number the alkane chain to show the location of the amine group.

  45. Carbonyl Group • When an oxygen is bound to a carbon by a double bond, it is called a carbonyl group. • Overhead “Functional Groups of Organic Compounds”

  46. Aldehydes • Aldehydes are organic compounds in which the carbonyl group is on the end carbon • Named by substituting “-al” for the final “-e” of the corresponding alkane name. • Methanal’s common name is “formaldehyde”

  47. Ketones • Ketones formed when carbonyl group is attached to an interior carbon atom that is attached to two other carbon atoms. • Named by replacing final “-e” of corresponding alkane name with “-one” • Propanone’s common name is “acetone” - nail polish remover. • Ketones are often used as solvents (because both polar and nonpolar

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