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  2. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5. Benzyl features a benzene ring ( C 6 H 6 ) attached to a methylene group ( −CH 2 − ).

  3. Formylation - Wikipedia

    en.wikipedia.org/wiki/Formylation

    Formyl functional group is shown in blue. Formylation refers to any chemical processes in which a compound is functionalized with a formyl group (-CH=O). In organic chemistry, the term is most commonly used with regards to aromatic compounds (for example the conversion of benzene to benzaldehyde in the Gattermann–Koch reaction).

  4. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    A cyclic compound or ring compound is a compound in which at least some its atoms are connected to form a ring. [1] Rings vary in size from three to many tens or even hundreds of atoms. Examples of ring compounds readily include cases where: all the atoms are carbon (i.e., are carbocycles),

  5. Simple aromatic ring - Wikipedia

    en.wikipedia.org/wiki/Simple_aromatic_ring

    Simple aromatic rings can be heterocyclic if they contain non-carbon ring atoms, for example, oxygen, nitrogen, or sulfur. They can be monocyclic as in benzene, bicyclic as in naphthalene, or polycyclic as in anthracene. Simple monocyclic aromatic rings are usually five-membered rings like pyrrole or six-membered rings like pyridine.

  6. Ring expansion and contraction - Wikipedia

    en.wikipedia.org/wiki/Ring_expansion_and_contraction

    Ring expansions can allow access to larger systems that can be difficult to synthesize otherwise. [6] Rings can be expanded by attack of the ring onto an outside group already appended to the ring (a migration/insertion), opening of a bicycle to a single larger ring, or coupling a ring closing with an expansion. [1]

  7. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Benzene is a natural constituent of petroleum and is one of the elementary petrochemicals. Due to the cyclic continuous pi bonds between the carbon atoms, benzene is classed as an aromatic hydrocarbon. Benzene is a colorless and highly flammable liquid with a sweet smell, and is partially responsible for the aroma of gasoline.

  8. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Identification of the ring or chain with the maximum number of senior groups. Identification of the ring or chain with the most senior elements (In order: N, P, Si, B, O, S, C). Identification of the parent compound. Rings are senior to chains if composed of the same elements. For cyclic systems: Identification of the parent cyclic ring.

  9. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    Heteroarenes are aromatic compounds, where at least one methine or vinylene (-C= or -CH=CH-) group is replaced by a heteroatom: oxygen, nitrogen, or sulfur. [3] Examples of non-benzene compounds with aromatic properties are furan, a heterocyclic compound with a five-membered ring that includes a single oxygen atom, and pyridine, a heterocyclic compound with a six-membered ring containing one ...