1/8
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
Aromatic Compound
Compound with unique structure and bonding due to delocalized electrons, like benzene.
Benzene
Aromatic compound; a ring of six carbon atoms with six hydrogen atoms and a ring of delocalized electrons. Very stable due to ring structure.
Arenes
Compounds containing benzene as part of their structure; also known as aromatic compounds. They tend to react via substitution mechanisms instead of addition.
Electrophilic Substitution
A reaction where an electrophile attacks the electron ring in benzene, partially destroying it, then the ring is restored. Types include: Halogenation, Nitration, and Friedel-Crafts Alkylation.
Halogenation of Benzene
Electrophilic substitution where a positively charged halide ion acts as an electrophile, forming a halobenzene compound.
Nitration of Benzene
Electrophilic substitution where the NO2+ ion is the electrophile, produced from the reaction of concentrated sulfuric acid and concentrated nitric acid.
Friedel-Crafts Alkylation
Reaction where the delocalized electron ring in benzene acts as a nucleophile, leading to an attack from acyl chlorides, using an aluminium chloride catalyst.
Phenylketone
The product of Friedel-Crafts alkylation; the benzene group is called a phenyl group.
Negative Inductive Effect
Effect where benzene rings draw electron density towards themselves, away from any substituent group such as a halogen atom, strengthening the bond.