1. Chapter 4 Alkenes: Structure, Nomenclature, Stability, and an Introduction to Reactivity (Part I) Essential Organic Chemistry Paula Yurkanis Bruice

2. Introduction sp 2 -sp 2  bond p-p  bond Alkenes contain a C=C double bond C=C double bond consists of

3. Introduction compared to alkanes, bond lengths decrease in alkenes compared to alkanes, bond angles increase in alkenes

4. Introduction  Typical representatives are Ethene, plant growth hormone, affects seed germination, flower maturation, and fruit ripening.

5. Introduction  Typical representatives are citronellol, in rose and geranium oils OH Geranium “Mavis Simpson” 23 4 5 6 1 2 3 4 5 6 1 7 8 7 8

6. Introduction  Typical representatives are limonene, in lemon and orange oils 2 3 4 5 6 1 2 34 5 6 1 Citrus limon

7. Introduction  Typical representatives are  -phellandrene, in oil of eucalyptus Eucalyptus globulus 2 3 4 5 6 1 2 3 4 5 6 1

8. 4.1 Molecular Formulas  Alkane: C n H 2n+2  Alkene: C n H 2n or C n H 2n+2- 2P P = number of double bonds + 2H

9. Molecular Formula  Alkane: C n H 2n+2  Ring: C n H 2n or C n H 2n+2- 2R R = number of rings + 2H

10. Molecular Formula  Alkene: C n H 2n+2- 2P-2R P = number of double bonds R = number of rings.

12. 4.2 Nomenclature of Alkenes  The functional group is the center of reactivity in a molecule.  The IUPAC system uses a suffix to denote certain functional groups.

13. Nomenclature of Alkenes  1-1. Find the longest carbon chain.  1-2. Enumerate the carbons such that the functional group, here the double bond, gets the lowest possible number.

14. Nomenclature of Alkenes  2. Substituents are cited before the parent longest chain, along with a number indicating its position at the chain.

15. Nomenclature of Alkenes  3. If a chain has more than one double bond, we first identify the chain by its alkane name, replacing the “ne” ending with the appropritate suffix: diene, triene, etc.  4. If a chain has more than one substitutent, substituents are cited in alphabetical order.

16. Nomenclature of Alkenes  5. If the same number for alkene is obtained in both directions, the correct name is the name that contains the lowest substituent number.

17. Nomenclature of Alkenes  6. A number is not needed to denote the position of the double bond in a cyclic alkene because the double bond is always placed between carbons 1 and 2.  7. Numbers are needed if the ring has more than one double bond.

18. Nomenclature of Alkenes  Remember that the name of a substituent is stated before the name of the parent hydrocarbon, and the functional group suffix is stated after that. [substitutent] [parent hydrocarbon] [fucntional group suffix]

19. Nomenclature of Alkenes

21. 4.3 The Structure of Alkenes  All six atoms of the double bond system are in the same plane.

23. 4.4 Cis-Trans Isomerism  Because rotation about a double bond does not readily occur, an alkene such as 2- butene can exist in two distinct forms.

24. cis/trans Isomers sp 2 -sp 2  bond p-p  bond side view p-i  bond front view The p-p  bond restricts free rotation.

25. cis/trans Isomers Upon rotation we lose p-p overlap, thus rotation doesn’t happen (easily). Consequently, geometrical isomers exist.

26. cis/trans Isomers All substituents are on one side of  bond All substituents are on different sides of  bond cis trans

29. cis/trans Isomers 1 23 4 5 cis-2-pentene 1 2 3 4 5 1 2 3 4 5

30. cis/trans Isomers 1 2 3 4 5 6 7 trans-3-heptene 1 2 3 4 5 6 7 1 2 3 4 5 6 7

31. cis/trans Isomers The main chain determines cis/trans in the name H 3 C CH 3 1 2 3 4 5 6 cis-3-methyl-2-hexene H 3 C CH 3 1 23 4 5 6 trans -3- methyl-2-hexene This compound is cis but the two methyl groups are … trans to each other. This compound is trans but the two methyl groups are … cis to each other. cis and trans are also used to designate the relative position of two groups.

33. 4.5 The E,Z System of Nomenclature For more than two substituents the cis/trans system cannot be used. To use the E/Z system we need to assign priorities to each substituent on each carbon. A new system, the E/Z system is introduced.

34. E/Z System In case high priorities are on the same side, we assign a Z configuration. In case high priorities are on opposite sides, we assign an E configuration.

35. E/Z System- Rule 1 The relative priorities of the two groups depend on the atomic numbers of the atoms bonded directly to the sp 2 carbon. The greater the atomic number, the higher is the priority of the group.

36. E/Z System Priorities are first assigned based on atomic numbers. I > C 1 2 F > H 1 2 (E)-3-fluoro-2-iodo-2-propene (Z)-3-fluoro-2-iodo-2-propene I > C 1 2 F > H 1 2

37. E/Z System- Rule 2 If the two substituents attached to the sp 2 carbon start with the same atom, you must move outward and consider the atomic numbers that are attached to the “tied” atoms.

38. E/Z System If you can’t decide using the first atoms attached, go out to the next atoms attached. If there are nonequivalent paths, always follow the path with atoms of higher atomic number. path goes to O, not H path goes to C, not H comparison stops here C H O H C H C H Z-configuration 1 2 1 2

39. E/Z System- Rule 3 If an atom is doubly (or triply) bonded to another atom, the priority system treats it as if it were singly bonded to two (or three) of those atoms.

40. E/Z System Atoms in double bonds are “replicated” at either end of the double bond. path goes to C, not H E-configuration 1 2 1 2