<?xml version="1.0"?>
<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en">
	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=2-Bromopropane</id>
	<title>2-Bromopropane - Revision history</title>
	<link rel="self" type="application/atom+xml" href="https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=2-Bromopropane"/>
	<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=2-Bromopropane&amp;action=history"/>
	<updated>2026-04-26T21:24:30Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
	<generator>MediaWiki 1.44.2</generator>
	<entry>
		<id>https://wikimd.org/index.php?title=2-Bromopropane&amp;diff=6310266&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=2-Bromopropane&amp;diff=6310266&amp;oldid=prev"/>
		<updated>2025-02-18T01:04:35Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 01:04, 18 February 2025&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l43&quot;&gt;Line 43:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 43:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Solvents]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Solvents]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Chemical compounds]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Chemical compounds]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;gallery&amp;gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;File:2-bromopropane-2D-skeletal.png|2-Bromopropane skeletal structure&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;File:2-bromopropane-2D-flat.png|2-Bromopropane flat structure&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;/gallery&amp;gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
	<entry>
		<id>https://wikimd.org/index.php?title=2-Bromopropane&amp;diff=6288361&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=2-Bromopropane&amp;diff=6288361&amp;oldid=prev"/>
		<updated>2025-02-11T20:28:18Z</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;= 2-Bromopropane =&lt;br /&gt;
&lt;br /&gt;
[[File:2-bromopropane-2D-skeletal.png|thumb|2D skeletal structure of 2-Bromopropane]]&lt;br /&gt;
[[File:2-bromopropane-2D-flat.png|thumb|2D flat structure of 2-Bromopropane]]&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;2-Bromopropane&amp;#039;&amp;#039;&amp;#039;, also known as &amp;#039;&amp;#039;&amp;#039;isopropyl bromide&amp;#039;&amp;#039;&amp;#039;, is an [[organobromine compound]] with the chemical formula C_H_Br. It is a colorless liquid that is used in various industrial applications, including as a solvent and an intermediate in organic synthesis.&lt;br /&gt;
&lt;br /&gt;
== Structure and Properties ==&lt;br /&gt;
2-Bromopropane is a [[haloalkane]] with a [[molecular structure]] consisting of a three-carbon [[alkane]] chain with a bromine atom attached to the second carbon. This structure gives it the [[IUPAC name]] 2-bromopropane. The presence of the bromine atom makes it a [[polar molecule]], which influences its physical and chemical properties.&lt;br /&gt;
&lt;br /&gt;
=== Physical Properties ===&lt;br /&gt;
2-Bromopropane is a colorless liquid at room temperature. It has a [[boiling point]] of approximately 59 °C and a [[density]] of about 1.31 g/cm_. It is slightly soluble in water but miscible with most organic solvents.&lt;br /&gt;
&lt;br /&gt;
=== Chemical Properties ===&lt;br /&gt;
As a haloalkane, 2-bromopropane is reactive in [[nucleophilic substitution reactions]]. It can undergo [[SN1]] and [[SN2 reactions]], depending on the conditions and the nucleophile involved. It is also susceptible to [[elimination reactions]], which can lead to the formation of [[alkenes]].&lt;br /&gt;
&lt;br /&gt;
== Synthesis ==&lt;br /&gt;
2-Bromopropane can be synthesized through the [[halogenation]] of [[propane]] using [[bromine]] in the presence of light or heat. Alternatively, it can be prepared by the reaction of [[isopropanol]] with [[hydrogen bromide]] in the presence of a strong acid catalyst.&lt;br /&gt;
&lt;br /&gt;
== Uses ==&lt;br /&gt;
2-Bromopropane is used in various industrial applications:&lt;br /&gt;
&lt;br /&gt;
* As a solvent in the manufacturing of [[pharmaceuticals]] and [[agrochemicals]].&lt;br /&gt;
* As an intermediate in the synthesis of other [[organic compounds]].&lt;br /&gt;
* In the production of [[flame retardants]] and [[plasticizers]].&lt;br /&gt;
&lt;br /&gt;
== Health and Safety ==&lt;br /&gt;
Exposure to 2-bromopropane can pose health risks. It is important to handle it with care, using appropriate [[personal protective equipment]] and following safety guidelines. Prolonged exposure can lead to [[respiratory]] and [[dermatological]] issues.&lt;br /&gt;
&lt;br /&gt;
== Related Pages ==&lt;br /&gt;
* [[Haloalkane]]&lt;br /&gt;
* [[Nucleophilic substitution]]&lt;br /&gt;
* [[Elimination reaction]]&lt;br /&gt;
* [[Organobromine compound]]&lt;br /&gt;
&lt;br /&gt;
== Gallery ==&lt;br /&gt;
&amp;lt;gallery&amp;gt;&lt;br /&gt;
File:2-bromopropane-2D-skeletal.png|2D skeletal structure of 2-Bromopropane&lt;br /&gt;
File:2-bromopropane-2D-flat.png|2D flat structure of 2-Bromopropane&lt;br /&gt;
&amp;lt;/gallery&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Organobromides]]&lt;br /&gt;
[[Category:Solvents]]&lt;br /&gt;
[[Category:Chemical compounds]]&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
</feed>