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===Reactivity=== {{see also|Clemmensen reduction}} Zinc has an [[electron configuration]] of [Ar]4s<sup>2</sup>3d<sup>10</sup> and is a member of the [[group 12 element|group 12]] of the [[periodic table]]. It is a moderately reactive [[metal]] and strong [[reducing agent]];<ref name="CRC2006p8-29">{{harvnb|CRC|2006|pp='''8'''β29}}</ref> in the [[reactivity series]] it is comparable to [[manganese]].<ref>{{cite video|first1=John W.|last1=Moore|first2=Lynn R.|last2=Hunsberger|first3=Steven D.|last3=Gammon|first4=Kelly|last4=Houston Jetzer|orig-date=6 Mar 2012|year=2022|title=Reaction of zinc with iodine|url=https://www.chemedx.org/video/reaction-zinc-iodine|type=web video|publisher=American Chemical Society, Division of Chemical Education|via=ChemEdX}}</ref> The surface of the pure metal [[tarnish]]es quickly, eventually forming a protective [[Passivation (chemistry)|passivating]] layer of the basic [[Hydrozincite|zinc carbonate]], {{chem|Zn|5|(OH)|6|(CO<sub>3</sub>)|2}}, by reaction with atmospheric [[carbon dioxide]].<ref>{{Cite book|publisher=CRC Press|date=1994|page=121|isbn=978-0-8247-9213-8|title=Corrosion Resistance of Zinc and Zinc Alloys| first=Frank C.|last=Porter}}</ref> Zinc burns in air with a bright bluish-green flame, giving off fumes of [[zinc oxide]].<ref name="Holl" /> Zinc reacts readily with [[acid]]s, [[alkali]]s and other non-metals.<ref>{{Cite book|last=Hinds|first=John Iredelle Dillard|title=Inorganic Chemistry: With the Elements of Physical and Theoretical Chemistry|publisher=John Wiley & Sons|location=New York|date=1908|edition=2nd|pages=506β508|url=https://books.google.com/books?id=xMUMAAAAYAAJ}}</ref> Extremely pure zinc reacts only slowly at [[room temperature]] with acids.<ref name="Holl" /> Strong acids, such as [[hydrochloric acid|hydrochloric]] or [[sulfuric acid]], can remove the passivating layer and the subsequent reaction with the acid releases hydrogen gas.<ref name="Holl" /> Zinc chemistry resembles that of the late first-row transition metals, [[nickel]] and copper,<ref name="Greenwood1997p1206" /> as well as certain [[main group element]]s. Almost all zinc compounds have the element in the +2 [[oxidation state]].<ref name=GenChem>{{Cite book|last=Brady|first=James E.|author2=Humiston, Gerard E.|author3=Heikkinen, Henry|title=General Chemistry: Principles and Structure|publisher=John Wiley & Sons|date=1983|edition=3rd|page=[https://archive.org/details/generalchemistry1982brad/page/671 671]|isbn=978-0-471-86739-5|url=https://archive.org/details/generalchemistry1982brad/page/671}}</ref> When Zn<sup>2+</sup> compounds form, the outer [[electron shell|shell]] ''s'' electrons are lost, yielding a bare zinc ion with the electronic configuration [Ar]3d<sup>10</sup>.<ref>{{Cite book|last=Ritchie|first=Rob|title=Chemistry|publisher=Letts and Lonsdale|date=2004|edition=2nd|page=71|isbn=978-1-84315-438-9|url=https://books.google.com/books?id=idT9j6406gsC}}</ref> The filled interior ''d'' shell generally does not participate in bonding, producing [[diamagnetic]] and mostly colorless compounds.<ref name="Greenwood1997p1206" /> In aqueous solution an octahedral complex, {{chem|[Zn(H|2|O)<sub>6</sub>]|2+}} is the predominant species.<ref>{{Cite book|last=Burgess|first=John|title=Metal ions in solution|publisher=Ellis Horwood|location=New York|date=1978|page=147|isbn=978-0-470-26293-1}}</ref> The [[ionic radii]] of zinc and magnesium happen to be nearly identical. Consequently some of the equivalent salts have the same [[crystal structure]],<ref>{{harvnb|CRC|2006|pp='''12'''β11β12}}</ref> and in other circumstances where ionic radius is a determining factor, the chemistry of zinc has much in common with that of magnesium.<ref name="Holl">{{Cite book|publisher=Walter de Gruyter|date=1985|edition=91β100| pages=1034β1041|isbn=978-3-11-007511-3|title=Lehrbuch der Anorganischen Chemie|first1=Arnold F.|last1=Holleman|last2=Wiberg|first2=Egon|last3=Wiberg|first3=Nils|language=de|chapter=Zink}}</ref> Compared to the transition metals, zinc tends to form bonds with a greater degree of [[covalency]]. [[Complex (chemistry)|Complexes]] with [[nitrogen|N]]- and [[sulfur|S]]- donors are much more stable.<ref name="Greenwood1997p1206">{{harvnb|Greenwood|Earnshaw|1997|p=1206}}</ref> Complexes of zinc are mostly 4- or 6- [[coordinate covalent bond|coordinate]], although 5-coordinate complexes are known.<ref name="Holl" /> Other oxidation states require unusual physical conditions, and the only positive oxidation states demonstrated are +1 or +2.<ref name=GenChem/> The [[volatilization]] of zinc in combination with zinc chloride at temperatures above 285 Β°C indicates the formation of {{chem|Zn|2|Cl|2}}, a zinc compound with a +1 oxidation state.<ref name="Holl" /> Calculations indicate that a zinc compound with the oxidation state of +4 is unlikely to exist.<ref>{{Cite journal|journal=Inorganic Chemistry|date=1994|volume=33|issue=10|pages=2122β2131|title=Oxidation state +IV in group 12 chemistry. Ab initio study of zinc(IV), cadmium(IV), and mercury(IV) fluorides|author=Kaupp M.|author2=Dolg M.|author3=Stoll H.|author4=Von Schnering H. G.|doi=10.1021/ic00088a012|url=https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-60018}}</ref> Zn(III) is predicted to exist in the presence of strongly electronegative trianions;<ref>{{cite journal |last1=Samanta |first1=Devleena |last2=Jena |first2=Puru |title=Zn in the +III Oxidation State |url=https://pubs.acs.org/doi/abs/10.1021/ja3029119# |journal=Journal of the American Chemical Society |date=2012|volume=134 |issue=20 |pages=8400β8403 |doi=10.1021/ja3029119 |pmid=22559713 |arxiv=1201.1014 |bibcode=2012JAChS.134.8400S }}</ref><ref>{{cite journal |last1=Fang |first1=Hong |last2=Banjade |first2=Huta |last3=Deepika |last4=Jena |first4=Puru |title=Realization of the Zn3+ oxidation state |journal=Nanoscale |date=2021|volume=13 |issue=33 |pages=14041β14048 |doi=10.1039/D1NR02816B |pmid=34477685 |s2cid=237400349 |doi-access=free }}</ref> however, there exists some doubt around this possibility.<ref>{{cite journal |last1=SchlΓΆder |first1=Tobias |display-authors=etal |title=Can Zinc Really Exist in Its Oxidation State +III? |url=https://pubs.acs.org/doi/10.1021/ja3052409# |journal=Journal of the American Chemical Society |date=2012|volume=134 |issue=29 |pages=11977β11979 |doi=10.1021/ja3052409 |pmid=22775535 |bibcode=2012JAChS.13411977S }}</ref>
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