Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Peroxide
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
{{Short description|Chemical compounds with the structure R–O–O–R'}} {{Other uses}} In [[chemistry]], '''peroxides''' are a group of [[Chemical compound|compounds]] with the structure {{chem2|R\sO\sO\sR}}, where the R's represent a radical (a portion of a complete molecule; not necessarily a [[free radical]]<ref>{{Cite web |title=Illustrated Glossary of Organic Chemistry |url=http://www.chem.ucla.edu/~harding/IGOC/R/r_group.html |access-date=June 19, 2024 |website=UCLA}}</ref>) and O's are single [[oxygen]] atoms.<ref>{{Greenwood&Earnshaw2nd}}</ref><ref>{{March6th}}</ref> Oxygen atoms are joined to each other and to adjacent elements through [[Single bond|single covalent bonds]], denoted by dashes or lines. The {{chem2|O\sO}} group in a peroxide is often called the '''peroxide group,''' though some nomenclature discrepancies exist. This linkage is recognized as a common [[polyatomic ion]], and exists in many molecules. == General structure == The characteristic structure of any regular peroxide is the oxygen–oxygen covalent single bond, which connects the two main atoms together. In the event that the molecule has no chemical [[Substituent|substituents]], the peroxide group will have a [−2] [[Formal charge|net charge]]. Each oxygen atom has a charge of negative one, as 5 of its [[Valence electron|valence electrons]] remain in the outermost [[Atomic orbital|orbital shell]] whilst one is occupied in the [[covalent bond]]. Because of the nature of the covalent bond, this arrangement results in each atom having the equivalent of 7 valence electrons, [[Redox|reducing]] the oxygens and giving them a negative charge. This charge is affected by the addition of other elements, with the properties and structure changing depending on the added group(s). == Common forms == [[File:Peroxide_group_v.2.png|left|thumb|324x324px|Types of peroxides, from top to bottom: peroxide ion, [[organic peroxide]], organic hydroperoxide, [[peracid]]. The peroxide group is marked in '''blue'''. R, R<sup>1</sup> and R<sup>2</sup> mark hydrocarbon [[Moiety (chemistry)|moieties]].]] The most common peroxide is [[hydrogen peroxide]] ({{chem2|H2O2}}), colloquially known simply as "peroxide". It is marketed as solutions in water at various concentrations. Many organic peroxides are known as well. In addition to hydrogen peroxide, some other major classes of peroxides are: * [[Peroxy acid|Peroxy acids]], the peroxy derivatives of many familiar acids, examples being [[peroxymonosulfuric acid]] and [[peracetic acid]], and their salts, one example of which is [[potassium peroxydisulfate]]. * [[Main group peroxides]], compounds with the linkage {{chem2|E\sO\sO\sE}} (E = [[main group element]]).{{multiple image | direction = vertical | align = right | header = | width = 215 | image1 = H2O2 gas structure.svg | alt1 = {{chem2|O\sO}} bond length = 147.4 pm <br />{{chem2|O\sH}} bond length = 95.0 pm | caption1 = Structure and dimensions of {{chem2|H2O2}} in gas phase. }} * [[Metal peroxide|Metal peroxides]], examples being [[barium peroxide]] ({{chem2|BaO2}}), [[sodium peroxide]] ({{chem2|Na2O2}}) and [[zinc peroxide]] ({{chem2|ZnO2}}). * [[Organic peroxide|Organic peroxides]], compounds with the linkage {{chem2|C\sO\sO\sC}} or {{chem2|C\sO\sO\sH}}. One example is [[Tert-Butyl hydroperoxide|''tert''-butylhydroperoxide]]. == Nomenclature == The linkage between the oxygen molecules is known as a '''peroxy group''' (sometimes called '''peroxo group,''' '''peroxyl group, of peroxy linkage'''). The nomenclature of the peroxy group is somewhat variable,<ref>{{GoldBookRef|title=peroxides|file=P04510}}</ref> and exists as an exception to the rules of naming polyatomic ions. This is because, when it was discovered, it was believed to be monatomic.<ref>{{Cite web |date=2004 |title=Nomenclature |url=https://chemed.chem.purdue.edu/genchem/topicreview/bp/ch2/names.html |access-date=March 25, 2024 |website=Purdue Division of Chemical Education}}</ref> The term was introduced by [[Thomas Thomson (chemist)|Thomas Thomson]] in 1804 for a compound combined with as much oxygen as possible,'''''<ref>{{Cite book |last=Thomson |first=Thomas |title=A System of Chemistry |date=1804 |publisher=Bell and Bradfute |edition=2nd |volume=1 |location=Edinburgh |publication-place=Edinburgh |publication-date=1804 |pages=division 1, page 103 |language=English |chapter=4 |via=Google books}}</ref>''''' or the oxide with the greatest quantity of oxygen.<ref>{{Cite web |last= Harper, Douglas. |title=Peroxide |url=https://www.etymonline.com/word/peroxide#:~:text=peroxide%20(n.),effective%20bleaching%20agent%20for%20hair). |website=Online Etymology Dictionary}}</ref> == References == <references /> {{Functional groups}} {{Authority control}} [[Category:Peroxides| ]]
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)
Pages transcluded onto the current version of this page
(
help
)
:
Template:Authority control
(
edit
)
Template:Chem2
(
edit
)
Template:Cite book
(
edit
)
Template:Cite web
(
edit
)
Template:Functional groups
(
edit
)
Template:GoldBookRef
(
edit
)
Template:Greenwood&Earnshaw2nd
(
edit
)
Template:March6th
(
edit
)
Template:Multiple image
(
edit
)
Template:Other uses
(
edit
)
Template:Short description
(
edit
)