# Phenyl group

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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. 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 functional group. Phenyl group has six carbon atoms bonded together in a hexagonal planar ring, five of which are bonded to individual hydrogen atoms, with the remaining carbon bonded to a substituent. Phenyl groups are commonplace in organic chemistry.[1] Although often depicted with alternating double and single bonds, phenyl group is chemically aromatic and has equal bond lengths between carbon atoms in the ring.[1][2]

## Nomenclature

Usually, a "phenyl group" is synonymous with C6H5 and is represented by the symbol Ph or, archaically, Φ. Benzene is sometimes denoted as PhH. Phenyl groups are generally attached to other atoms or groups. For example, triphenylmethane (Ph3CH) has three phenyl groups attached to the same carbon center. Many or even most phenyl compounds are not described with the term "phenyl". For example, the chloro derivative C6H5Cl is normally called chlorobenzene, although it could be called phenyl chloride. In special (and rare) cases, isolated phenyl groups are detected: the phenyl anion (C6H5), the phenyl cation (C6H+5), and the phenyl radical (C
6
H
5
).

Although Ph and phenyl uniquely denote C6H5, substituted derivatives also are described using the phenyl terminology. For example, C6H4NO2 is nitrophenyl, and C6F5 is pentafluorophenyl. Monosubstituted phenyl groups (that is, disubstituted benzenes) are associated with electrophilic aromatic substitution reactions and the products follow the arene substitution pattern. So, a given substituted phenyl compound has three isomers, ortho (1,2-disubstitution), meta (1,3-disubstitution) and para (1,4-disubstitution). A disubstituted phenyl compound (trisubstituted benzene) may be, for example, 1,3,5-trisubstituted or 1,2,3-trisubstituted. Higher degrees of substitution, of which the pentafluorophenyl group is an example, exist and are named according to IUPAC nomenclature.

### Etymology

Phenyl is derived from French phényle, which in turn derived from Greek φαίνω (phaino) 'shining', as the first phenyl compounds named were byproducts of making and refining various gases used for lighting.[3] According to McMurry, "The word is derived from Greek pheno 'I bear light', commemorating the discovery of benzene by Michael Faraday in 1825 from the oily residue left by the illuminating gas used in London street lamps."[4]

## Structure, bonding, and characterization

Phenyl compounds are derived from benzene (C6H6), at least conceptually and often in terms of their production. In terms of its electronic properties, the phenyl group is related to a vinyl group. It is generally considered an inductively withdrawing group (-I), because of the higher electronegativity of sp2 carbon atoms, and a resonance donating group (+M), due to the ability of its π system to donate electron density when conjugation is possible.[5] The phenyl group is hydrophobic. Phenyl groups tend to resist oxidation and reduction. Phenyl groups (like all aromatic compounds) have enhanced stability in comparison to equivalent bonding in aliphatic (non-aromatic) groups. This increased stability is due to the unique properties of aromatic molecular orbitals.[2]

The bond lengths between carbon atoms in a phenyl group are approximately 1.4 Å.[6]

In 1H-NMR spectroscopy, protons of a phenyl group typically have chemical shifts around 7.27 ppm. These chemical shifts are influenced by aromatic ring current and may change depending on substituents.

## Preparation, occurrence, and applications

Phenyl groups are usually introduced using reagents that behave as sources of the phenyl anion or the phenyl cation. Representative reagents include phenyllithium (C6H5Li) and phenylmagnesium bromide (C6H5MgBr). Electrophiles are attacked by benzene to give phenyl derivatives:

${\displaystyle {\ce {C6H6 + E+ -> C6H5E + H+}}}$

where E+ (the "electrophile") = Cl+, NO+2, SO3. These reactions are called electrophilic aromatic substitutions.

Phenyl groups are found in many organic compounds, both natural and synthetic (see figure). Most common among natural products is the amino acid phenylalanine, which contains a phenyl group. A major product of the petrochemical industry is "BTX" consisting of benzene, toluene, and xylene - all of which are building blocks for phenyl compounds. The polymer polystyrene is derived from a phenyl-containing monomer and owes its properties to the rigidity and hydrophobicity of the phenyl groups. Many drugs as well as many pollutants contain phenyl rings. One of the simplest phenyl-containing compounds is phenol, C6H5OH. It is often said the resonance stability of phenol makes it a stronger acid than that of aliphatic alcohols such as ethanol (pKa = 10 vs. 16–18). However, a significant contribution is the greater electronegativity of the sp2 alpha carbon in phenol compared to the sp3 alpha carbon in aliphatic alcohols.[7]

## References

1. ^ a b March, Jerry (1992). Advanced organic chemistry: reactions, mechanisms, and structure (4th ed.). New York: Wiley. ISBN 978-0-471-60180-7.
2. ^ a b "Aromaticity. Benzene and Other Aromatic Compounds". Virtual Textbook of Organic Chemistry. Michigan State University.
3. ^ "phenyl". English by Lexico Dictionaries. Archived from the original on February 16, 2013. Retrieved 24 July 2019.
4. ^ McMurry, John E. (2009). Organic Chemistry, Enhanced Edition. Cengage Learning. p. 518. ISBN 9781111790042.
5. ^ Hansch, Corwin.; Leo, A.; Taft, R. W. (1991-03-01). "A survey of Hammett substituent constants and resonance and field parameters". Chemical Reviews. 91 (2): 165–195. doi:10.1021/cr00002a004. ISSN 0009-2665.
6. ^ Hameka, Hendrik F. (1987). "Computation of the structures of the phenyl and benzyl radicals with the UHF method". The Journal of Organic Chemistry. 52 (22): 5025–5026. doi:10.1021/jo00231a035. ISSN 0022-3263.
7. ^ Silva, Pedro Jorge (2009). "Inductive and Resonance Effects on the Acidities of Phenol, Enols, and Carbonyl α-Hydrogens". The Journal of Organic Chemistry. 74 (2): 914–916. doi:10.1021/jo8018736. hdl:10284/3294. ISSN 0022-3263. PMID 19053615.