《有机化学》课程PPT教学课件（Official PPT of Organic Chemistry, 8th Edition, L. G. Wade, Jr.Pearson Education）Chapter 15 Conjugated Systems, Orbital Symmetry, and Ultraviolet Spectroscopy

Organic Chemistry, ORGANIC 8th Edition CHEMISTRY L.G.Wade,Jr. Chapter 15 Lecture Conjugated Systems, Orbital Symmetry,and Ultraviolet Spectroscopy G.WADE,J R 2013 Pearson Education,Inc. ALWAYS LEARNING PEARSON

© 2013 Pearson Education, Inc. Chapter 15 1 Chapter 15 Lecture Organic Chemistry, 8 th Edition L. G. Wade, Jr. Conjugated Systems, Orbital Symmetry, and Ultraviolet Spectroscopy © 2013 Pearson Education, Inc

Conjugated Systems c-c-☒ conjugated double bonds penta-1,3-diene (more stable than isolated double bonds) H、 H、 H >c=Cc=c< CH, CH2 isolated double bonds penta-1,4-diene Conjugated double bonds are separated by one single bond. Isolated double bonds are separated by two or more single bonds Conjugated double bonds are more stable than isolated ones. 2013 Pearson Education,Inc. Chapter 15

© 2013 Pearson Education, Inc. Chapter 15 2 Conjugated Systems • Conjugated double bonds are separated by one single bond. • Isolated double bonds are separated by two or more single bonds. • Conjugated double bonds are more stable than isolated ones

Heat of Hydrogenation of Conjugated Bonds ◇入 pent-1-ene trans-pent-2-ene predicted Predicted: -126kJ -116kJ -242kJ(-57.7kcal) 2H2 Pt actual value -225kJ(-53.7kcal) trans-penta-1,3-diene more stable by 17 kJ (4.0 kcal) Conjugated double bonds have extra stability. cumulated terminal diene alkyne penta-1.2-diene pent-1-yne alkyne 202kJ pent-2-yne (69.8 keal isolated 到 291kJ diene (69.5 keal) isolated 275k penta-1.4-dien diene (65.8 keal) 入 trans-hexa-1,4-dicne conjugated 252」 diene (60.2 keal 242 (57.7 keal trans-penta-1.3-diene 225J (53.7 kcal)- alkane (pentane or hexane) 2013 Pearson Education,Inc. Chapter 15 3

© 2013 Pearson Education, Inc. Chapter 15 3 Heat of Hydrogenation of Conjugated Bonds ▪ Conjugated double bonds have extra stability

Structure of Buta-1.3-diene small amount of overlap partial double bond H 1.34A 1.48A L.34A The C2-C3 single bond is shorter than 1.54 A. Electrons are delocalized over the molecule. The C2-C3 bond,has a partial double bond character. 2013 Pearson Education,Inc. Chapter 15

© 2013 Pearson Education, Inc. Chapter 15 4 Structure of Buta-1,3-diene ▪ The C2—C3 single bond is shorter than 1.54 Å. ▪ Electrons are delocalized over the molecule. ▪ The C2—C3 bond, has a partial double bond character

Molecular Orbitals(MOs) -Each p orbital has two lobes with the wave function indicated by plus (+)and minus(-) sign (not electrical charges). -When lobes overlap constructively (and + or-and-),a pi bonding (MO is formed. -When lobes overlap destructively (and-), a pi antibonding(π*）MO is formed. 2013 Pearson Education,Inc. Chapter 15 5

© 2013 Pearson Education, Inc. Chapter 15 5 Molecular Orbitals (MOs) ▪ Each p orbital has two lobes with the wave function indicated by plus (+) and minus (–) sign (not electrical charges). ▪ When lobes overlap constructively (+ and +, or – and –), a pi bonding (p) MO is formed. ▪ When lobes overlap destructively (+ and –), a pi antibonding (p*) MO is formed

Ethylene Pi MOs node (antibonding)= destructive overlap energy of the isolated orbitals on CI and C2 energy (bonding)= constructive overlap The combination of two p orbitals must give two molecular orbitals. ■ Constructive overlap is a pi bonding()MO. Destructive overlap is an antibonding (*MO. 2013 Pearson Education,Inc. Chapter 15

© 2013 Pearson Education, Inc. Chapter 15 6 Ethylene Pi MOs ▪ The combination of two p orbitals must give two molecular orbitals. ▪ Constructive overlap is a pi bonding (p) MO. ▪ Destructive overlap is an antibonding (p*) MO

MO for Buta-1,3-diene bonding bonding bonding ·Lowest energy. Electrons are delocalized over 4 nuclei. 2013 Pearson Education,Inc. Chapter 15

© 2013 Pearson Education, Inc. Chapter 15 7 p1 MO for Buta-1,3-diene ▪ Lowest energy. ▪ Electrons are delocalized over 4 nuclei

2 MO for Buta-1,3-diene bonding antibonding bonding node This is a bonding MO. Higher energy than MO and not as strong. 2013 Pearson Education,Inc. Chapter 15

© 2013 Pearson Education, Inc. Chapter 15 8 p2 MO for Buta-1,3-diene ▪ This is a bonding MO. ▪ Higher energy than p1 MO and not as strong

3*MO for Buta-1,3-diene antibonding antibonding bonding 3 node node 2013 Pearson Education,Inc. Chapter 15 9

© 2013 Pearson Education, Inc. Chapter 15 9 p3 * MO for Buta-1,3-diene

MO for Buta-1,3-diene all antibonding 4 node node node 2013 Pearson Education,Inc. Chapter 15 10

© 2013 Pearson Education, Inc. Chapter 15 10 p4 * MO for Buta-1,3-diene