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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Nitro_compound</id>
	<title>Nitro compound - Revision history</title>
	<link rel="self" type="application/atom+xml" href="https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Nitro_compound"/>
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	<updated>2026-05-13T01:54:01Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.org/index.php?title=Nitro_compound&amp;diff=6321841&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Nitro_compound&amp;diff=6321841&amp;oldid=prev"/>
		<updated>2025-02-18T11:08:18Z</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;
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				&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 11:08, 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-l27&quot;&gt;Line 27:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 27:&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;br&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;br&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;{{Chemistry-stub}}&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;{{Chemistry-stub}}&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;
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&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:PhNO2&amp;amp;metric.png|Phenyl nitro compound with metric dimensions&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:Benzol.svg|Benzene structure&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
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&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:Nitrohydrogenation.svg|Nitrohydrogenation process&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
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&lt;/table&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
	<entry>
		<id>https://wikimd.org/index.php?title=Nitro_compound&amp;diff=5436370&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Nitro_compound&amp;diff=5436370&amp;oldid=prev"/>
		<updated>2024-03-22T03:36:56Z</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;&amp;#039;&amp;#039;&amp;#039;Nitro compounds&amp;#039;&amp;#039;&amp;#039; are organic compounds that contain one or more nitro functional groups (-NO2). These groups are attached to a carbon atom in a molecule. Nitro compounds are a diverse class of organic compounds with a wide range of applications and properties, from explosives to pharmaceuticals. The nitro group is electron-withdrawing, which significantly affects the chemical behavior of the compound.&lt;br /&gt;
&lt;br /&gt;
==Chemistry==&lt;br /&gt;
Nitro compounds are characterized by the presence of the nitro group, which consists of one nitrogen atom bonded to two oxygen atoms (N=O&amp;gt;O). This group is typically bonded to a carbon atom in an organic compound. The presence of the nitro group can significantly alter the chemical and physical properties of the molecule, making nitro compounds highly reactive in some cases.&lt;br /&gt;
&lt;br /&gt;
===Synthesis===&lt;br /&gt;
Nitro compounds can be synthesized through various chemical reactions. One common method is the nitration of aromatic compounds using nitric acid, often in the presence of sulfuric acid as a catalyst. This process involves the substitution of a hydrogen atom on the aromatic ring with a nitro group. Aliphatic nitro compounds can also be synthesized through the reaction of alkenes with nitric acid or through the nitration of alkanes.&lt;br /&gt;
&lt;br /&gt;
===Reactions===&lt;br /&gt;
Nitro compounds undergo a range of chemical reactions. They can be reduced to amines, which is a critical step in the synthesis of many pharmaceuticals and dyes. Nitro compounds can also participate in nucleophilic substitution reactions, where the nitro group is replaced by other groups. Additionally, the presence of the nitro group can facilitate the formation of other functional groups, such as carbonyls, through specific oxidation reactions.&lt;br /&gt;
&lt;br /&gt;
==Applications==&lt;br /&gt;
Nitro compounds have a wide range of applications in various fields. In the pharmaceutical industry, nitro compounds are precursors to a variety of drugs, including antibiotics and analgesics. In the agricultural sector, some nitro compounds serve as herbicides and insecticides. Nitro compounds are also used in the production of dyes, polymers, and explosives. Nitroglycerin, a well-known nitro compound, is used both as a heart medication and as an explosive.&lt;br /&gt;
&lt;br /&gt;
==Safety and Environmental Impact==&lt;br /&gt;
Nitro compounds, especially those used as explosives, are handled with caution due to their potential for detonation. Proper storage and handling procedures are essential to prevent accidental explosions. In the environment, nitro compounds can be toxic to aquatic life and may contribute to water and soil pollution. Bioremediation and chemical degradation are methods used to mitigate the environmental impact of nitro compounds.&lt;br /&gt;
&lt;br /&gt;
==See Also==&lt;br /&gt;
* [[Organic chemistry]]&lt;br /&gt;
* [[Functional group]]&lt;br /&gt;
* [[Nitration]]&lt;br /&gt;
* [[Amine]]&lt;br /&gt;
* [[Explosive]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Organic compounds]]&lt;br /&gt;
[[Category:Nitro compounds]]&lt;br /&gt;
&lt;br /&gt;
{{Chemistry-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
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