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32 relations: Arene substitution pattern, Aromatic ring current, Arsenic trichloride, Benzene, Bismabenzene, Borabenzene, Chemical equilibrium, Covalent bond, Diels–Alder reaction, Diene, Dimer (chemistry), Electrophilic aromatic substitution, Friedel–Crafts reaction, Germabenzene, Heterocyclic compound, Hexafluoro-2-butyne, International Union of Pure and Applied Chemistry, Lewis acids and bases, Ligand, Nuclear magnetic resonance spectroscopy, Organoarsenic chemistry, Organotin chemistry, Periodic table, Phosphine, Phosphorine, Polyyne, Pyridine, Pyrylium salt, Silabenzene, Simple aromatic ring, Stannabenzene, Trifluoroacetic acid.
Arene substitution pattern
Arene substitution patterns are part of organic chemistry IUPAC nomenclature and pinpoint the position of substituents other than hydrogen in relation to each other on an aromatic hydrocarbon.
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Aromatic ring current
An aromatic ring current is an effect observed in aromatic molecules such as benzene and naphthalene.
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Arsenic trichloride
Arsenic trichloride is an inorganic compound with the formula AsCl3, also known as arsenous chloride or butter of arsenic.
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Benzene
Benzene is an important organic chemical compound with the chemical formula C6H6.
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Bismabenzene
Bismabenzene (C5H5Bi) is the parent representative of a group of organobismuth compounds that are related to benzene with a carbon atom replaced by a bismuth atom.
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Borabenzene
A borabenzene is a heteroaromatic compound that has a boron atom instead of the carbon atom of a benzene molecule.
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Chemical equilibrium
In a chemical reaction, chemical equilibrium is the state in which both reactants and products are present in concentrations which have no further tendency to change with time, so that there is no observable change in the properties of the system.
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Covalent bond
A covalent bond, also called a molecular bond, is a chemical bond that involves the sharing of electron pairs between atoms.
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Diels–Alder reaction
The Diels–Alder reaction is an organic chemical reaction (specifically, a cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene derivative.
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Diene
In organic chemistry a diene or diolefin is a hydrocarbon that contains two carbon double bonds.
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Dimer (chemistry)
A dimer (di-, "two" + -mer, "parts") is an oligomer consisting of two monomers joined by bonds that can be either strong or weak, covalent or intermolecular.
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Electrophilic aromatic substitution
Electrophilic aromatic substitution is an organic reaction in which an atom that is attached to an aromatic system (usually hydrogen) is replaced by an electrophile.
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Friedel–Crafts reaction
The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring.
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Germabenzene
Germabenzene (C5H6Ge) is the parent representative of a group of chemical compounds containing in their molecular structure a benzene ring with a carbon atom replaced by a germanium atom.
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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).
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Hexafluoro-2-butyne
Hexafluoro-2-butyne is the fluorocarbon with the formula CF3C≡CCF3.
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International Union of Pure and Applied Chemistry
The International Union of Pure and Applied Chemistry (IUPAC) is an international federation of National Adhering Organizations that represents chemists in individual countries.
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Lewis acids and bases
A Lewis acid is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct.
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Ligand
In coordination chemistry, a ligand is an ion or molecule (functional group) that binds to a central metal atom to form a coordination complex.
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Nuclear magnetic resonance spectroscopy
Nuclear magnetic resonance spectroscopy, most commonly known as NMR spectroscopy or magnetic resonance spectroscopy (MRS), is a spectroscopic technique to observe local magnetic fields around atomic nuclei.
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Organoarsenic chemistry
Organoarsenic chemistry is the chemistry of compounds containing a chemical bond between arsenic and carbon.
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Organotin chemistry
Organotin compounds or stannanes are chemical compounds based on tin with hydrocarbon substituents.
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Periodic table
The periodic table is a tabular arrangement of the chemical elements, ordered by their atomic number, electron configuration, and recurring chemical properties, whose structure shows periodic trends.
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Phosphine
Phosphine (IUPAC name: phosphane) is the compound with the chemical formula PH3.
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Phosphorine
Phosphorine (IUPAC name: phosphinine) is a heavier element analog of pyridine, containing a phosphorus atom instead of an aza- moiety.
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Polyyne
In chemistry, a polyyne is any organic compound with alternating single and triple bonds; that is, a series of consecutive alkynes, with n greater than 1.
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Pyridine
Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N.
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Pyrylium salt
The pyrylium cation is a six-membered, unsaturated, mono-cyclic compound.
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Silabenzene
A silabenzene is a heteroaromatic compound containing one or more silicon atoms instead of carbon atoms in benzene.
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Simple aromatic ring
Simple aromatic rings, also known as simple arenes or simple aromatics, are aromatic organic compounds that consist only of a conjugated planar ring system.
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Stannabenzene
Stannabenzene (C5H6Sn) is the parent representative of a group of organotin compounds that are related to benzene with a carbon atom replaced by a tin atom.
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Trifluoroacetic acid
Trifluoroacetic acid (TFA) is an organofluorine compound with the chemical formula CF3CO2H.
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References
[1] https://en.wikipedia.org/wiki/Arsabenzene
