Chapter 16 Aromatic Compounds 有机化学英文版教学课件（美国达拉斯社区学院） 《Organic Chemistry 5th Edition (L.G. Wade JR.)》.pptVIP

Chapter 16 Chapter 16Aromatic Compounds Jo Blackburn Richland College, Dallas, TX Dallas County Community College District ? 2003, Prentice Hall Discovery of Benzene Isolated in 1825 by Michael Faraday who determined C:H ratio to be 1:1. Synthesized in 1834 by Eilhard Mitscherlich who determined molecular formula to be C6H6. Other related compounds with low C:H ratios had a pleasant smell, so they were classified as aromatic.  = Kekulé Structure Proposed in 1866 by Friedrich Kekulé, shortly after multiple bonds were suggested. Failed to explain existence of only one isomer of 1,2-dichlorobenzene. Resonance Structure Each sp2 hybridized C in the ring has an unhybridized p orbital perpendicular to the ring which overlaps around the ring. Unusual Reactions Alkene + KMnO4 ? diol (addition)Benzene + KMnO4 ? no reaction. Alkene + Br2/CCl4 ? dibromide (addition)Benzene + Br2/CCl4 ? no reaction. With FeCl3 catalyst, Br2 reacts with benzene to form bromobenzene + HBr (substitution!). Double bonds remain. = Unusual Stability Hydrogenation of just one double bond in benzene is endothermic! Annulenes All cyclic conjugated hydrocarbons were proposed to be aromatic. However, cyclobutadiene is so reactive that it dimerizes before it can be isolated. And cyclooctatetraene adds Br2 readily. Look at MO’s to explain aromaticity. = MO Rules for Benzene Six overlapping p orbitals must form six molecular orbitals. Three will be bonding, three antibonding. Lowest energy MO will have all bonding interactions, no nodes. As energy of MO increases, the number of nodes increases. = MO’s for Benzene Energy Diagram for Benzene The six electrons fill three bonding pi orbitals. All bonding orbitals are filled (“closed shell”), an extremely stable arrangement. MO’s for Cyclobutadiene Energy Diagram forCyclo