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  2. Heterocyclic compound - Wikipedia

    en.wikipedia.org/wiki/Heterocyclic_compound

    A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). [1] Heterocyclic organic chemistry is the branch of organic chemistry dealing with the synthesis, properties, and applications of organic heterocycles .

  3. Alkyne trimerisation - Wikipedia

    en.wikipedia.org/wiki/Alkyne_trimerisation

    An alkyne trimerisation is a [2+2+2] cycloaddition reaction in which three alkyne units (C≡C) react to form a benzene ring. The reaction requires a metal catalyst. The process is of historic interest as well as being applicable to organic synthesis. [1] Being a cycloaddition reaction, it has high atom economy.

  4. Simple aromatic ring - Wikipedia

    en.wikipedia.org/wiki/Simple_aromatic_ring

    Many simple aromatic rings have trivial names. They are usually found as substructures of more complex molecules ("substituted aromatics"). Typical simple aromatic compounds are benzene, indole, and pyridine. [1] [2] Simple aromatic rings can be heterocyclic if they contain non-carbon ring atoms, for example, oxygen, nitrogen, or sulfur.

  5. Metal-centered cycloaddition reactions - Wikipedia

    en.wikipedia.org/wiki/Metal-centered_cyclo...

    There are two general types of metal-centered cycloaddition reactions: those in which the metal is incorporated into the cycle (a metallocycle), and those in which the metal is external to the cycle. These can be further divided into "true" cycloadditions (those that take place in a concerted fashion), and formal cycloadditions (those that take ...

  6. Aromaticity - Wikipedia

    en.wikipedia.org/wiki/Aromaticity

    Two different resonance forms of benzene (top) combine to produce an average structure (bottom). In organic chemistry, aromaticity is a chemical property describing the way in which a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals exhibits a stabilization stronger than would be expected from conjugation alone.

  7. Electrophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    The nitration of benzene is achieved via the action of the nitronium ion as the electrophile. The sulfonation with fuming sulfuric acid gives benzenesulfonic acid. Aromatic halogenation with bromine, chlorine, or iodine gives the corresponding aryl halides. This reaction is typically catalyzed by the corresponding iron or aluminum trihalide.

  8. Sandwich compound - Wikipedia

    en.wikipedia.org/wiki/Sandwich_compound

    Structure of (Me 4 N +) 2 [Fe(C 2 B 9 H 11) 2] +, showing only one Me 4 N +. [4] Closely related are the metal complexes containing H 3 C 3 B 2 R 2 ligands. [7] In addition to these, other sandwich complexes containing purely inorganic ligands are known, such as Fe(C 5 Me 5)(P 5) and [(P 5) 2 Ti] 2−. [8]

  9. Phenyl group - Wikipedia

    en.wikipedia.org/wiki/Phenyl_group

    In organic chemistry, the phenyl group, or phenyl ring, is a cyclic group of atoms with the formula C6H5, and is often represented by the symbol Ph (archaically φ) or Ø. The phenyl group is closely related to benzene and can be viewed as a benzene ring, minus a hydrogen, which may be replaced by some other element or compound to serve as a ...