1 / 10

Aromatic Compounds

Aromatic Compounds. 1. 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 C 6 H 6 .

forest
Download Presentation

Aromatic Compounds

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Aromatic Compounds 1

  2. 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. =>

  3. => 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.

  4. => Resonance Structure Each sp2 hybridized C in the ring has an unhybridized p orbital perpendicular to the ring which overlaps around the ring.

  5. 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. =>

  6. Unusual Stability Hydrogenation of just one double bond in benzene is endothermic! =>

  7. 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. =>

  8. 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. =>

  9. MO’s for Benzene =>

  10. => Energy Diagram for Benzene The six electrons fill three bonding pi orbitals. All bonding orbitals are filled (“closed shell”), an extremely stable arrangement.

More Related