Chapter 13 Alkenes and Alkynes Based on Material Prepared by Andrea D. Leonard University of Louisiana at Lafayette

Transcription

1 Chapter 13 Alkenes and Alkynes Based on Material Prepared by Andrea D. Leonard University of Louisiana at Lafayette 1 Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

2 Alkenes and Alkynes Alkenes and alkynes are two families of hydrocarbons that contain multiple bonds. Alkenes are compounds that contain a carbon carbon double bond. Alkenes have the general formula C n H 2n. 2

3 Alkenes and Alkynes Alkynes are compounds that contain a carbon carbon triple bond. Alkynes have the general formula C n H 2n 2. 3

4 Alkenes and Alkynes Alkenes and alkynes are composed of nonpolar bonds. Their physical properties are like those of alkanes. Alkenes and alkynes have low melting and boiling points, and are insoluble in water. They are called unsaturated hydrocarbons because they contain fewer than the maximum number of H atoms per C. 4

5 Alkenes and Alkynes The multiple bond is always drawn in a condensed structure. 5

6 Nomenclature of Alkenes and Alkynes HOW TO Name an Alkene or Alkyne Example Give the IUPAC name of each alkene and alkyne. Step [1] Find the longest chain that contains both C atoms of the double or triple bond. 6

7 Nomenclature of Alkenes and Alkynes HOW TO Name an Alkene or Alkyne 4 C s in longest chain butane butene Since the compound is an alkene, change the ane ending to ene. 6 C s in longest chain hexane hexyne Since the compound is an alkyne, change the ane ending to yne. 7

8 Nomenclature of Alkenes and Alkynes HOW TO Name an Alkene or Alkyne Step [2] Number the carbon chain from the end that gives the multiple bond the lower number. 1-butene 2-hexyne Name the compound using the first number assigned to the multiple bond. 8

9 Nomenclature of Alkenes and Alkynes HOW TO Name an Alkene or Alkyne Step [3] Number and name the substituents, and write the name. 9

10 Nomenclature of Alkenes and Alkynes HOW TO Name an Alkene or Alkyne Step [3] Number and name the substituents, and write the name. 10

11 Nomenclature of Alkenes and Alkynes Compounds with two double bonds are called dienes. Dienes are named by changing the ane ending of the parent alkane to adiene. Each double bond gets its own number ,3-butadiene 5-methyl-1,4-hexadiene 11

12 Nomenclature of Alkenes and Alkynes When naming cycloalkenes, the double bond is located between C1 and C2. The 1 is usually omitted in the name. The ring is numbered to give the first substituent the lower number CH 3 CH 3 1-methylcyclopentene CH 3 1,6-dimethylcyclohexene 6 12

13 Cis Trans Isomers A. Stereoisomers A New Class of Isomer There is no rotation around the C atoms of a double bond. 2-butene Therefore, 2-butene has two possible arrangements: two CH 3 groups on the same side cis isomer two CH 3 groups on opposite sides trans isomer 13

14 Cis Trans Isomers A. Stereoisomers A New Class of Isomer 14

15 Cis Trans Isomers A. Stereoisomers A New Class of Isomer When the two groups on one end of the double bond are identical (e.g., both H or both CH 3 ), no cis and trans isomers are possible. 15

16 Cis Trans Isomers A. Stereoisomers A New Class of Isomer Stereoisomers are isomers that differ only in the spatial arrangement of atoms. Constitutional isomers differ in the way the atoms are bonded to each other. 16

17 Cis Trans Isomers B. Saturated and Unsaturated Fatty Acids Fatty acids are carboxylic acids (RCOOH) with long carbon chains of carbon atoms. Naturally occurring animal fats and vegetable oils are formed from fatty acids. Saturated fatty acids have no double bonds in their long hydrocarbon chains. Unsaturated fatty acids have one or more double bonds in their long hydrocarbon chains. 17

18 Cis Trans Isomers B. Saturated and Unsaturated Fatty Acids 18

19 Interesting Alkenes in Food and Medicine Lycopene, the red pigment in tomatoes and watermelons, has 13 double bonds. Lycopene is an antioxidant, a compound that prevents unwanted oxidation from occurring. Diets containing high levels of antioxidants result in decreased risk of heart disease and cancer. 19

20 Reactions of Alkenes Alkenes undergo addition reactions wherein new groups X and Y are added to the alkene. One bond of the double bond is broken and two new single bonds are formed. 20

21 Reactions of Alkenes 21

22 Reactions of Alkenes A. Addition of Hydrogen Hydrogenation Hydrogenation is the addition of H 2 to an alkene. The metal catalyst (usually palladium Pd) speeds up the rate of the reaction. The product of hydrogenation is an alkane. 22

23 Reactions of Alkenes A. Addition of Hydrogen Hydrogenation Example of hydrogenation: 23

24 Reactions of Alkenes B. Addition of Halogen Halogenation Halogenation is the addition of halogen (X 2 ) to an alkene. X 2 is usually Cl 2 or Br 2. Halogenation occurs readily and does not require a catalyst. The product of halogenation is a dihalide. 24

25 Reactions of Alkenes B. Addition of Halogen Halogenation Examples of halogenation: 25

26 Reactions of Alkenes C. Addition of Hydrogen Halides Hydrohalogenation Hydrohalogenation is the addition of HX (HCl or HBr) to an alkene. The product of hydrohalogenation is an alkyl halide. 26

27 Reactions of Alkenes C. Addition of Hydrogen Halides Hydrohalogenation Examples of hydrohalogenation: 27

28 Reactions of Alkenes C. Addition of Hydrogen Halides Hydrohalogenation If the reactant is an asymmetrical alkene, its is possible to form two products. These two potential products are constitutional isomers. 28

29 Reactions of Alkenes C. Addition of Hydrogen Halides Hydrohalogenation However, only one of the two products will actually form in more abundance. Markovnikov s rule states that the H atom of H X will bond to the less substituted C atom in the C C double bond. It means that the C in the double bond with the most H s will bond to the H atom of H X. 29

30 Reactions of Alkenes C. Addition of Hydrogen Halides Hydrohalogenation Looking at the reaction again: 30

31 Reactions of Alkenes C. Addition of Hydrogen Halides Hydrohalogenation Looking at the reaction again: 31

32 Reactions of Alkenes D. Addition of Water Hydration Hydration is the addition of water to an alkene. Hydration requires a strong acid, H 2 SO 4. The product formed by hydration is an alcohol. 32

33 Reactions of Alkenes D. Addition of Water Hydration An example of hydration: 33

34 Reactions of Alkenes D. Addition of Water Hydration If the reactant is an asymmetrical alkene, the product will be determined by Markovnikov s rule. 34

35 Focus on Health and Medicine Margarine or Butter? Butter is made up of saturated fatty acid chains. A diet rich in saturated fatty acids stimulate an excessive production of cholesterol. Scientists have attempted to produce alternative versions of butter (margarine) with similar taste and properties, but with some C C double bonds (i.e., unsaturated fatty acid chains). 35

36 Focus on Health and Medicine Margarine or Butter? 36

37 Focus on Health and Medicine Margarine or Butter? Unfortunately, some partial hydrogenations leave trans double bonds on the fatty acid chain. Trans fatty acids are very similar in shape to saturated fatty acids. Trans fatty acids have the same effects as saturated fatty acids: stimulate cholesterol production. 37

38 Polymers Polymers are large molecules made up of repeating units of smaller molecules (monomers) covalently bonded together. 38

39 Polymers A. Synthetic Polymers In polymerization, the monomer C C double bonds are broken and single bonds linking the monomers together are formed. 39

40 Polymers A. Synthetic Polymers 40

41 Aromatic Compounds Aromatic compounds are compounds that contain a benzene ring. Each C is trigonal planar (i.e., 120 bond angles), making benzene a planar molecule. 41

42 Aromatic Compounds Each of these representations has the same arrangement of atoms, but different locations of electrons. These are resonance structures, and the true structure is with all three electron pairs in the double bonds delocalized. It is usually represented as follow: 42

43 Aromatic Compounds Aromatic hydrocarbons do not undergo the addition reactions that characterize alkenes. 43

44 Nomenclature of Benzene Derivatives A. Monosubstituted Benzenes To name a benzene ring with one substituent: Name the substituent first Then add the word benzene at the end 44

45 Nomenclature of Benzene Derivatives A. Monosubstituted Benzenes Some monosubstituted benzenes have common names that you must learn. 45

46 Nomenclature of Benzene Derivatives B. Disubstituted Benzenes 46

47 Nomenclature of Benzene Derivatives B. Disubstituted Benzenes If there are two groups on the benzene ring and they are different, alphabetize the two substituent names. 47

48 Nomenclature of Benzene Derivatives B. Disubstituted Benzenes If one of the two substituents is part of a common root, then name the molecule as a derivative of that monosubstituted benzene. 48

49 Nomenclature of Benzene Derivatives C. Polysubstituted Benzenes 1. Number to give the lowest possible numbers around the ring. 2. Alphabetize the substituent names. 3. When the substituents are part of common roots: Name the molecule as a derivative of that monosubstituted benzene Put the common root substituent at C1, but omit the 1 from the name 49

50 Nomenclature of Benzene Derivatives C. Polysubstituted Benzenes Assign the lowest set of numbers. Alphabetize the names of all the substituents. 4-chloro-1-ethyl-2-propylbenzene 50

51 Nomenclature of Benzene Derivatives C. Polysubstituted Benzenes Name the molecule as a derivative of the common root aniline. Assign the NH 2 group to position 1 and then assign the lowest possible set of numbers to the other groups. 2,5-dichloroaniline 51

52 Nomenclature of Benzene Derivatives D. Aromatic Compounds with More than One Ring 52

53 Focus on Health and Medicine Aromatic Drugs Some common drugs that contain benzene rings are: 53

54 Focus on Health and Medicine Phenols as Antioxidants

55 Reactions of Aromatic Compounds Aromatic compounds undergo substitution reactions primarily. Substitution is a reaction in which an atom is replaced by another atom or group of atoms. Substitution of H by X keeps the stable aromatic ring intact. 55

56 Reactions of Aromatic Compounds A. Chlorination and DDT In chlorination, a Cl atom substitutes for a hydrogen atom on the benzene ring. The pesticide DDT is formed by a chlorination reaction. 56

57 Reactions of Aromatic Compounds B. Nitration and Sulfa Drugs Benzene reacts with nitric acid (HNO 3 ) in the presence of sulfuric acid (H 2 SO 4 ) to form nitrobenzene. Nitration is a valuable reaction because nitro gropus are readily converted into amino groups. 57

58 Reactions of Aromatic Compounds B. Nitration and Sulfa Drugs Sulfa drugs, such as the antibacterial agents shown below, are formed by the nitration reaction. 58

59 Reactions of Aromatic Compounds C. Sulfonation and Detergent Synthesis In sulfonation, benzene reacts with SO 3 in the presence of H 2 SO 4 such that a SO 3 H group substitutes for a hydrogen atom on the benzene ring. The synthetic detergent shown is a product of sulfonation. 59