| 1. | Both the phenyl and the naphthanol group are aromatic ring systems.
|
| 2. | The term can also be extended to substituents on aromatic rings.
|
| 3. | The ?-electropositive effect introduces electrons into the aromatic ring.
|
| 4. | Examples of activated aromatic rings are toluene, aniline and phenol.
|
| 5. | These allow Claisen-like reactions to occur, generating aromatic rings.
|
| 6. | Polycarbonate molecules ( such as the aromatic ring ) absorb UV radiation.
|
| 7. | Fused aromatic rings consist of monocyclic rings that share their connecting bonds.
|
| 8. | Typical examples of basic aromatic rings are pyridine or quinoline.
|
| 9. | FAD is an aromatic ring system, whereas FADH 2 is not.
|
| 10. | Cyclooctatetraene also undergoes rearrangement reactions to form aromatic ring systems.
|
