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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Cyclopropane</id>
	<title>Cyclopropane - Revision history</title>
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	<updated>2026-05-12T14:28:40Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wikimd.org/index.php?title=Cyclopropane&amp;diff=5806114&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Cyclopropane&amp;diff=5806114&amp;oldid=prev"/>
		<updated>2024-05-22T15:41:34Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[File:Regular_triangle.svg|thumb|Regular_triangle.svg]] &amp;#039;&amp;#039;&amp;#039;Cyclopropane&amp;#039;&amp;#039;&amp;#039; is a [[cycloalkane]] molecule with the molecular formula C₃H₆, consisting of three carbon atoms arranged in a ring, with each carbon atom bonded to two hydrogen atoms. It is the simplest cycloalkane and is notable for its unique properties and historical significance in [[anesthesia]].&lt;br /&gt;
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==Structure and Bonding==&lt;br /&gt;
Cyclopropane is characterized by a triangular ring structure, which creates significant [[ring strain]] due to the 60° bond angles between the carbon atoms. This strain makes cyclopropane more reactive than other cycloalkanes. The carbon-carbon bonds in cyclopropane are bent and exhibit [[banana bond]]ing, which is a type of bonding that helps to alleviate some of the ring strain.&lt;br /&gt;
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==Synthesis==&lt;br /&gt;
Cyclopropane can be synthesized through several methods, including the [[Simmons-Smith reaction]], which involves the reaction of [[diiodomethane]] with a [[zinc-copper couple]] in the presence of an [[alkene]]. Another method is the [[Wurtz reaction]], where [[1,3-dibromopropane]] is treated with [[sodium]] metal.&lt;br /&gt;
&lt;br /&gt;
==Reactivity==&lt;br /&gt;
Due to its ring strain, cyclopropane is more reactive than other cycloalkanes. It readily undergoes reactions such as [[hydrogenation]], [[halogenation]], and [[polymerization]]. Cyclopropane can also participate in [[ring-opening reactions]], which relieve the ring strain and form more stable compounds.&lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
Historically, cyclopropane was used as an [[inhalational anesthetic]] due to its rapid onset and potency. However, its use has declined due to the development of safer and more effective anesthetics. Cyclopropane is also used in [[organic synthesis]] as a building block for more complex molecules.&lt;br /&gt;
&lt;br /&gt;
==Safety and Handling==&lt;br /&gt;
Cyclopropane is highly flammable and forms explosive mixtures with air. It should be handled with care, and appropriate safety measures should be taken to prevent accidental ignition.&lt;br /&gt;
&lt;br /&gt;
==See Also==&lt;br /&gt;
* [[Cycloalkane]]&lt;br /&gt;
* [[Anesthesia]]&lt;br /&gt;
* [[Ring strain]]&lt;br /&gt;
* [[Simmons-Smith reaction]]&lt;br /&gt;
* [[Wurtz reaction]]&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{Reflist}}&lt;br /&gt;
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==External Links==&lt;br /&gt;
{{Commons category|Cyclopropane}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Cycloalkanes]]&lt;br /&gt;
[[Category:Anesthetics]]&lt;br /&gt;
[[Category:Organic compounds]]&lt;br /&gt;
[[Category:Hydrocarbons]]&lt;br /&gt;
[[Category:Chemical compounds]]&lt;br /&gt;
&lt;br /&gt;
{{medicine-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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