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		<title>Nomenclature of Alkyl Halides</title>
		<link>https://thefactfactor.com/facts/pure_science/chemistry/organic-chemistry/nomenclature-of-alkyl-halides/12030/</link>
					<comments>https://thefactfactor.com/facts/pure_science/chemistry/organic-chemistry/nomenclature-of-alkyl-halides/12030/#respond</comments>
		
		<dc:creator><![CDATA[Hemant More]]></dc:creator>
		<pubDate>Tue, 21 Apr 2020 14:09:07 +0000</pubDate>
				<category><![CDATA[Organic Chemistry]]></category>
		<category><![CDATA[1-Bromopropane]]></category>
		<category><![CDATA[1-Chlorobutane]]></category>
		<category><![CDATA[2-Chloropropane]]></category>
		<category><![CDATA[2-Chlro butane]]></category>
		<category><![CDATA[Alkyl bromides]]></category>
		<category><![CDATA[Alkyl chlorides]]></category>
		<category><![CDATA[Alkyl halides]]></category>
		<category><![CDATA[Alkyl iodides]]></category>
		<category><![CDATA[Boiling points of alkyl halides]]></category>
		<category><![CDATA[Bromo propane]]></category>
		<category><![CDATA[Bromobutane]]></category>
		<category><![CDATA[Bromoethane]]></category>
		<category><![CDATA[Bromomethane]]></category>
		<category><![CDATA[Chain isomerism]]></category>
		<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[Chemistry of carbon compounds]]></category>
		<category><![CDATA[Chloroethane]]></category>
		<category><![CDATA[Chloromethane]]></category>
		<category><![CDATA[Chloropropane]]></category>
		<category><![CDATA[Common system of nomenclature]]></category>
		<category><![CDATA[Density of alkyl halides]]></category>
		<category><![CDATA[Dihalogen derivatives of alkanes]]></category>
		<category><![CDATA[Dipole moment]]></category>
		<category><![CDATA[Ethyl bromide]]></category>
		<category><![CDATA[Ethyl chloride]]></category>
		<category><![CDATA[Ethyl iodide]]></category>
		<category><![CDATA[Haloalkane]]></category>
		<category><![CDATA[Halogen derivatives of alkanes]]></category>
		<category><![CDATA[Iodo ethane]]></category>
		<category><![CDATA[Iodobutane]]></category>
		<category><![CDATA[Iodomethane]]></category>
		<category><![CDATA[Iodopropane]]></category>
		<category><![CDATA[Iso-propyl chloride]]></category>
		<category><![CDATA[Isomerism]]></category>
		<category><![CDATA[IUPAC system]]></category>
		<category><![CDATA[Methyl bromide]]></category>
		<category><![CDATA[Methyl chloride]]></category>
		<category><![CDATA[Methyl iodide]]></category>
		<category><![CDATA[Monohaloen derivatives of alkanes]]></category>
		<category><![CDATA[n-propyl bromide]]></category>
		<category><![CDATA[Optical isomerism]]></category>
		<category><![CDATA[Organic chemistry]]></category>
		<category><![CDATA[Polyhalogen derivatives of alkanes]]></category>
		<category><![CDATA[Position isomerism]]></category>
		<category><![CDATA[Primary alkyl halides]]></category>
		<category><![CDATA[Sec-butyl bromide]]></category>
		<category><![CDATA[Secondary alkyl halides]]></category>
		<category><![CDATA[Solubility of alkyl halides]]></category>
		<category><![CDATA[Tertiary alkyl halides]]></category>
		<category><![CDATA[Trihalogen derivatives of alkanes]]></category>
		<category><![CDATA[Trivial system]]></category>
		<guid isPermaLink="false">https://thefactfactor.com/?p=12030</guid>

					<description><![CDATA[<p>Science &#62; Chemistry &#62; Halogen Derivatives of Alkanes &#62; Nomenclature of Alkyl Halides In this article, we shall study isomerism in alkyl halides and their nomenclature. Isomerism in Haloalkanes:&#160; Isomers are the organic compounds, which have the same molecular formula but different structural formula and properties. The phenomenon is called isomerism.&#160;Haloalkanes can exhibit the following [&#8230;]</p>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/organic-chemistry/nomenclature-of-alkyl-halides/12030/">Nomenclature of Alkyl Halides</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
]]></description>
										<content:encoded><![CDATA[
<h4 class="wp-block-heading"><strong>Science &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/" target="_blank">Chemistry</a> &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/halogen-derivatives-of-alkanes/" target="_blank">Halogen Derivatives of Alkanes</a> &gt; Nomenclature of Alkyl Halides</strong></h4>



<p>In this article, we shall study isomerism in alkyl halides and their nomenclature.</p>



<p class="has-text-color has-background has-medium-font-size has-luminous-vivid-orange-color has-very-light-gray-background-color"><strong>Isomerism in Haloalkanes:&nbsp;</strong></p>



<p>Isomers are the organic compounds, which have the same molecular formula but different structural formula and properties. The phenomenon is called isomerism.&nbsp;Haloalkanes can exhibit the following type of isomerism.</p>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Chain Isomerism:</strong></p>



<p>The haloalkanes with four or more carbon atoms exhibit this type of isomerism. This isomerism is exhibited due to the difference in the carbon chains.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img decoding="async" width="344" height="70" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-16.png" alt="" class="wp-image-12032" srcset="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-16.png 344w, https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-16-300x61.png 300w" sizes="(max-width: 344px) 100vw, 344px" /></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Position Isomerism:</strong></p>



<p>The haloalkanes with three or more carbon atoms exhibit this type of isomerism. This isomerism is exhibited due to the difference in the position of halogen group.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img decoding="async" width="300" height="78" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-17.png" alt="" class="wp-image-12034"/></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Optical Isomerism:</strong></p>



<p>The haloalkanes which have the same molecular and structural formula, but have a different arrangement of the atoms or group of atoms in space and have a tendency to rotate the plane of polarised light are called optical isomers and the phenomenon is called optical isomerism.</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img decoding="async" width="264" height="145" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-18.png" alt="" class="wp-image-12036"/></figure></div>



<p class="has-text-color has-background has-medium-font-size has-luminous-vivid-orange-color has-very-light-gray-background-color"><strong>More Examples:</strong></p>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Isomers of monochloro derivatives of 2,3-Dimethylbutane:</strong></p>



<p class="has-text-align-center">Structure of 2,3-Dimethylbutane is</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="142" height="46" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-19.png" alt="Alkyl Halides" class="wp-image-12038"/></figure></div>



<p class="has-text-align-center">The isomers of monochloro derivatives of 2,3-Dimethylbutane are</p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="414" height="80" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-20.png" alt="" class="wp-image-12039" srcset="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-20.png 414w, https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-20-300x58.png 300w" sizes="auto, (max-width: 414px) 100vw, 414px" /></figure></div>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Isomers of C<sub>5</sub>H<sub>11</sub>Br and their classification:</strong></p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="264" height="161" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-21.png" alt="" class="wp-image-12041"/></figure></div>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="293" height="435" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-22.png" alt="" class="wp-image-12043" srcset="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-22.png 293w, https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-22-202x300.png 202w" sizes="auto, (max-width: 293px) 100vw, 293px" /></figure></div>



<p><strong>Note: </strong>2 &#8211; Bromo-2-methylbutane, 2 &#8211; Bromo-3-methylbutane, 1 &#8211; Bromo-3-methylbutane are enantiomers. i.e. they are optically active compounds</p>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Isomers of&nbsp;C<sub>4</sub>H<sub>9</sub>Br&nbsp;and their classification:&nbsp;</strong></p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="300" height="268" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-23.png" alt="" class="wp-image-12045"/></figure></div>



<p class="has-text-color has-background has-medium-font-size has-luminous-vivid-orange-color has-very-light-gray-background-color"><strong>Classification of alkyl halides:</strong></p>



<p><strong>1-Bromopropane&nbsp;</strong></p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="169" height="40" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-24.png" alt="" class="wp-image-12047"/></figure></div>



<p>Bromine atom is attached to a primary carbon i.e. this carbon is attached to only one carbon atom. Hence it is primary alkyl halide.</p>



<p><strong>2-Bromopropane&nbsp;</strong></p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="149" height="43" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-25.png" alt="" class="wp-image-12049" srcset="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-25.png 149w, https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-25-144x43.png 144w" sizes="auto, (max-width: 149px) 100vw, 149px" /></figure></div>



<p>Bromine atom is attached to a secondary carbon i.e. this carbon is attached to two other carbon atoms. Hence it is secondary alkyl halide.</p>



<p><strong>2-Bromo-2-methylpropane</strong></p>



<div class="wp-block-image"><figure class="aligncenter size-large"><img loading="lazy" decoding="async" width="156" height="60" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-26.png" alt="" class="wp-image-12051"/></figure></div>



<p>Bromine atom is attached to a tertiary carbon i.e. this carbon is attached to three other carbon atoms. Hence it is tertiary alkyl halide.</p>



<p class="has-text-color has-background has-medium-font-size has-luminous-vivid-orange-color has-very-light-gray-background-color"><strong>Nomenclature:</strong></p>



<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>Trivial or Common System of Nomenclature:</strong></p>



<p>In the trivial system, haloalkanes are named as alkyl halides. The name is derived by adding the word halide to the name of the corresponding alkyl group. The trivial name is always written as two separate words.</p>



<p>e.g. CH<sub>3</sub>Br (Methyl bromide), CH<sub>3</sub>CH<sub>2</sub>Br (Ethyl bromide), CH<sub>3</sub>CH<sub>2</sub>Cl (Ethyl chloride).</p>



<h4 class="wp-block-heading"><strong>Different Alkyl Groups With Examples:</strong></h4>


<table align="center" border="1">
<tbody>
<tr>
<td style="text-align: center;" width="47">
<p><strong>Sr.</strong></p>
</td>
<td style="text-align: center;" width="248">
<p><strong>Alkyl Group</strong></p>
</td>
<td style="text-align: center;" width="128">
<p><strong>Name of&nbsp;Group</strong></p>
</td>
<td style="text-align: center;" width="217">
<p><strong>Example</strong></p>
</td>
<td>
<p style="text-align: center;"><strong>Compound Name</strong></p>
</td>
</tr>
<tr>
<td width="47">
<p>1</p>
</td>
<td width="248">
<p>CH<sub>3</sub>–</p>
</td>
<td width="128">
<p>Methyl</p>
</td>
<td width="217">
<p>CH<sub>3</sub>Cl</p>
</td>
<td>
<p>Methyl chloride</p>
</td>
</tr>
<tr>
<td width="47">
<p>2</p>
</td>
<td width="248">
<p>CH<sub>3</sub>CH<sub>2</sub>–&nbsp; or&nbsp;C<sub>2</sub>H<sub>5</sub>–</p>
</td>
<td width="128">
<p>Ethyl</p>
</td>
<td width="217">
<p>C<sub>2</sub>H<sub>5</sub>Br</p>
</td>
<td>
<p>Ethyl bromide</p>
</td>
</tr>
<tr>
<td width="47">
<p>3</p>
</td>
<td width="248">
<p>CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>–</p>
</td>
<td width="128">
<p>n-Propyl</p>
</td>
<td width="217">
<p>CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>I</p>
</td>
<td>
<p>n-Propyl iodide</p>
</td>
</tr>
<tr>
<td width="47">
<p>4</p>
</td>
<td width="248"><img loading="lazy" decoding="async" class="alignnone size-full wp-image-12053 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-27.png" alt="" width="113" height="37"></td>
<td width="128">
<p>iso-Propyl</p>
</td>
<td width="217">
<p>CH<sub>3</sub>CHBrCH<sub>3</sub></p>
</td>
<td width="160">
<p>iso-Propyl bromide</p>
</td>
</tr>
<tr>
<td width="47">
<p>5</p>
</td>
<td width="248">
<p>CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>–</p>
</td>
<td width="128">
<p>n-Butyl</p>
</td>
<td width="217">
<p>CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>I</p>
</td>
<td width="160">
<p>n-Butyl iodide</p>
</td>
</tr>
<tr>
<td width="47">
<p>6</p>
</td>
<td width="248"><img loading="lazy" decoding="async" class="alignnone size-full wp-image-12054 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-28.png" alt="" width="150" height="41"></td>
<td width="128">
<p>sec-Butyl</p>
</td>
<td width="217">
<p>CH<sub>3</sub>CHClCH<sub>2</sub>CH<sub>3</sub></p>
</td>
<td width="160">
<p>sec-Butyl iodide</p>
</td>
</tr>
<tr>
<td width="47">
<p>7</p>
</td>
<td width="248"><img loading="lazy" decoding="async" class="size-full wp-image-12056 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-29.png" alt="" width="122" height="46" srcset="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-29.png 122w, https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-29-120x46.png 120w" sizes="auto, (max-width: 122px) 100vw, 122px" /></td>
<td width="128">
<p>iso-Butyl</p>
</td>
<td width="217"><img loading="lazy" decoding="async" class="size-full wp-image-12057 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-30.png" alt="" width="131" height="44"></td>
<td width="160">
<p>iso-Butyl chloride</p>
</td>
</tr>
<tr>
<td width="47">
<p>8</p>
</td>
<td width="248"><img loading="lazy" decoding="async" class="alignnone size-full wp-image-12058 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-31.png" alt="" width="91" height="72"></td>
<td width="128">
<p>tert-Butyl</p>
</td>
<td width="217"><img loading="lazy" decoding="async" class="size-full wp-image-12059 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-32.png" alt="" width="85" height="68"></td>
<td width="160">
<p>tert-Butyl bromide</p>
</td>
</tr>
<tr>
<td width="47">
<p>9</p>
</td>
<td width="248"><img loading="lazy" decoding="async" class="size-full wp-image-12060 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-33.png" alt="" width="115" height="72"></td>
<td width="128">
<p>neo-Pentyl</p>
</td>
<td width="217"><img loading="lazy" decoding="async" class="alignnone size-full wp-image-12061 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-34.png" alt="" width="143" height="68"></td>
<td width="160">
<p>neo-Pentylbromide</p>
</td>
</tr>
</tbody>
</table>


<p class="has-text-color has-medium-font-size has-vivid-red-color"><strong>IUPAC Nomenclature:</strong></p>



<figure class="wp-block-table"><table><tbody><tr><td><strong>No.</strong></td><td><strong>Formula</strong></td><td><strong>Common Name</strong></td><td><strong>IUPAC Name</strong></td></tr><tr><td>1</td><td>CH<sub>3</sub>Br</td><td>methyl bromide</td><td>Bromomethane</td></tr><tr><td>2</td><td>CH<sub>3</sub>CH<sub>2</sub>Br</td><td>ethyl bromide</td><td>Bromoethane</td></tr><tr><td>3</td><td>CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>Cl</td><td>n-propyl chloride</td><td>1-Chloropropane</td></tr><tr><td>4</td><td>CH<sub>3</sub>CHClCH<sub>3</sub></td><td>isopropyl chloride</td><td>2-Chloropropane</td></tr><tr><td>5</td><td>CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>Cl</td><td>n-butyl chloride</td><td>1-Chlorobutane</td></tr><tr><td>6</td><td>CH<sub>3</sub>CHClCH<sub>2</sub>CH<sub>3</sub></td><td>sec-butyl chloride</td><td>2-Chlorobutane</td></tr><tr><td>7</td><td>(CH<sub>3</sub>)<sub>2</sub>CHCH<sub>2</sub>I</td><td>isobutyl iodide</td><td>1-Iodo-2-methylpropane</td></tr><tr><td>8</td><td>(CH<sub>3</sub>)<sub>3</sub>CBr</td><td>tert-butyl bromide</td><td>2-Bromo-2-methylpropane</td></tr><tr><td>9</td><td>(CH<sub>3</sub>)<sub>3</sub>CCH<sub>2</sub>Br</td><td>neo-pentyl bromide</td><td>1-Bromo-2,2-dimethylpropane</td></tr><tr><td>10</td><td>CH<sub>2</sub>=CHCl</td><td>vinyl chloride</td><td>Chloroethene</td></tr><tr><td>11</td><td>CH<sub>2</sub>=CHCH<sub>2</sub>Cl</td><td>allyl chloride</td><td>3-Chloroprop-1-ene</td></tr></tbody></table></figure>



<h4 class="wp-block-heading"><strong>To Draw Structure From IUPAC Name:</strong></h4>


<table border="1" align="center">
<tbody>
<tr>
<td width="47">
<p style="text-align: center;"><strong>No.</strong></p>
</td>
<td style="text-align: center;" width="360">
<p><strong>IUPAC Name</strong></p>
</td>
<td width="392">
<p style="text-align: center;"><strong>Structure</strong></p>
</td>
</tr>
<tr>
<td width="47">
<p>1</p>
</td>
<td width="360">
<p>2-Iodo-3-methylpentane</p>
</td>
<td width="392"><img loading="lazy" decoding="async" class="alignnone size-full wp-image-12063 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-35.png" alt="" width="204" height="47"></td>
</tr>
<tr>
<td width="47">
<p>2</p>
</td>
<td width="360">
<p>3-Chlorohexane</p>
</td>
<td width="392"><img loading="lazy" decoding="async" class="alignnone size-full wp-image-12064 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-36.png" alt="" width="248" height="48"></td>
</tr>
<tr>
<td width="47">
<p>3</p>
</td>
<td width="360">
<p>1-Chloro-2,2-dimethylpropane</p>
</td>
<td width="392"><img loading="lazy" decoding="async" class="alignnone size-full wp-image-12065 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-37.png" alt="" width="140" height="77"></td>
</tr>
<tr>
<td width="47">
<p>4</p>
</td>
<td width="360">
<p>3-Bromo-2-methylpentane</p>
</td>
<td width="392"><img loading="lazy" decoding="async" class="alignnone size-full wp-image-12067 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-38.png" alt="" width="193" height="47"></td>
</tr>
<tr>
<td width="47">
<p>5</p>
</td>
<td width="360">
<p>2-Bromo-3-ethyl-2-methylhexane</p>
</td>
<td width="392"><img loading="lazy" decoding="async" class="size-full wp-image-12068 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-39.png" alt="" width="202" height="67"></td>
</tr>
<tr>
<td width="47">
<p>6</p>
</td>
<td width="360">
<p>1-Chlorobutane</p>
</td>
<td width="392">
<p style="text-align: center;">CH<sub>3</sub>-CH<sub>2</sub>-CH<sub>2</sub>-CH<sub>2</sub>Cl</p>
</td>
</tr>
<tr>
<td width="47">
<p>7</p>
</td>
<td width="360">
<p>2-Bromo-2-methylpentane</p>
</td>
<td width="392"><img loading="lazy" decoding="async" class="alignnone size-full wp-image-12069 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-40.png" alt="" width="207" height="73"></td>
</tr>
<tr>
<td width="47">
<p>8</p>
</td>
<td width="360">
<p>1-chloro-2,2-dimethylpropane</p>
</td>
<td width="392"><img loading="lazy" decoding="async" class="size-full wp-image-12070 aligncenter" src="https://thefactfactor.com/wp-content/uploads/2020/04/Halogen-Derivatives-of-Alkanes-41.png" alt="" width="134" height="71"></td>
</tr>
</tbody>
</table>


<h4 class="wp-block-heading"><strong>Science &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/" target="_blank">Chemistry</a> &gt; <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/halogen-derivatives-of-alkanes/" target="_blank">Halogen Derivatives of Alkanes</a> &gt; Nomenclature of Alkyl Halides</strong></h4>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/organic-chemistry/nomenclature-of-alkyl-halides/12030/">Nomenclature of Alkyl Halides</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
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