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		<title>Preparation of Alkyl Halides by Halide Exchange Method</title>
		<link>https://thefactfactor.com/facts/pure_science/chemistry/organic-chemistry/preparation-of-alkyl-halides-by-halide-exchange-method/15590/</link>
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		<dc:creator><![CDATA[Hemant More]]></dc:creator>
		<pubDate>Fri, 27 Nov 2020 11:15:49 +0000</pubDate>
				<category><![CDATA[Organic Chemistry]]></category>
		<category><![CDATA[(Finkelstein Reaction]]></category>
		<category><![CDATA[Alkyl halides]]></category>
		<category><![CDATA[Borodine Hunsdiecker Reaction]]></category>
		<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[Chemistry of carbon compounds]]></category>
		<category><![CDATA[Dihalogen derivatives of alkanes]]></category>
		<category><![CDATA[Halide exchange method]]></category>
		<category><![CDATA[Halogen derivatives of alkanes]]></category>
		<category><![CDATA[Monohaloen derivatives of alkanes]]></category>
		<category><![CDATA[Organic chemistry]]></category>
		<category><![CDATA[Polyhalogen derivatives of alkanes]]></category>
		<category><![CDATA[Swart’s Reaction]]></category>
		<category><![CDATA[Trihalogen derivatives of alkanes]]></category>
		<guid isPermaLink="false">https://thefactfactor.com/?p=15590</guid>

					<description><![CDATA[<p>Science > Chemistry > Organic Chemistry > Halogen Derivatives of Alkanes > Preparation of Alkyl Halides by Halide Exchange Method In the last three articles, we have studied the methods of preparations of alkyl halides from alkanes, alkenes, alcohols. In this article, we shall study the method of the preparation of alkyl halids by halide [&#8230;]</p>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/organic-chemistry/preparation-of-alkyl-halides-by-halide-exchange-method/15590/">Preparation of Alkyl Halides by Halide Exchange Method</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
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<h5 class="wp-block-heading"><strong>Science > <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/" target="_blank">Chemistry</a> > Organic Chemistry > <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/halogen-derivatives-of-alkanes/" target="_blank">Halogen Derivatives of Alkanes</a> > Preparation of Alkyl Halides by Halide Exchange Method</strong></h5>



<p>In the last three articles, we have studied the methods of preparations of alkyl halides from alkanes, alkenes, alcohols. In this article, we shall study the method of the preparation of alkyl halids by halide exchange method. This method is typical for preparations of alkyl iodides/fluorides/bromides.</p>



<p class="has-accent-color has-text-color has-large-font-size"><strong>Preparation of Alkyl iodides by Halide Exchange Method(Finkelstein Reaction)</strong></p>



<h5 class="wp-block-heading"><strong>General Reaction:</strong></h5>



<p>When alkyl chlorides or bromides when treated with NaI in presence of dry acetone give alkyl iodides.</p>



<p class="has-text-align-center">R–Cl or R–Br  +  NaI → RI + NaCl  or NaBr</p>



<p class="has-text-align-center">Alkyl chloride / bromide&nbsp;&nbsp; sodium iodide&nbsp; &nbsp;→ &nbsp; &nbsp;Alkyl iodide sodium chloride / bromide</p>



<h5 class="wp-block-heading"><strong>Example &#8211; 1: Preparation of Ethyl iodide (Iodoethane) from ethyl chloride (Chloroethane):</strong></h5>



<p class="has-text-align-center">C<sub>2</sub>H<sub>5</sub>-Cl&nbsp;&nbsp;&nbsp; +&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; NaI <img decoding="async" width="114" height="32" class="wp-image-15592" style="width: 114px;" src="https://thefactfactor.com/wp-content/uploads/2020/11/Halide-Exchange-Method-01.png" alt="Halide Exchange Method" align="middle">&nbsp; C<sub>2</sub>H<sub>5</sub>I&nbsp; &nbsp; &nbsp; +&nbsp;&nbsp; NaCl</p>



<p class="has-text-align-center">Ethyl chloride    sodium iodide    Ethyl iodide  sodium chloride</p>



<h5 class="wp-block-heading"><strong>Example &#8211; 2: Preparation of Ethyl iodide (Iodoethane) from ethyl bromide (Bromoethane):</strong></h5>



<p class="has-text-align-center">C<sub>2</sub>H<sub>5</sub>-Br&nbsp;&nbsp;&nbsp; +&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; NaI <img decoding="async" width="114" height="32" align="middle" class="wp-image-15592" style="width: 114px;" src="https://thefactfactor.com/wp-content/uploads/2020/11/Halide-Exchange-Method-01.png" alt="Halide Exchange Method">&nbsp; C<sub>2</sub>H<sub>5</sub>I&nbsp; &nbsp; &nbsp; +&nbsp;&nbsp; NaBr</p>



<p class="has-text-align-center">Ethyl bromide    sodium iodide   Ethyl iodide       sodium bromide</p>



<p class="has-accent-color has-text-color has-large-font-size"><strong>Preparation of Alkyl fluorides by Halide Exchange Method(Swart’s Reaction):</strong></p>



<p>The direct reaction of alkanes with fluorine is highly explosive in nature, hence it can’t be produced by direct fluorination of alkanes.</p>



<h5 class="wp-block-heading"><strong>General Reaction:</strong></h5>



<p>When alkyl halides are treated with salts like AgF, Hg<sub>2</sub>F<sub>2</sub>, CoF<sub>3</sub>, SbF<sub>3</sub> fluoroalkanes can be obtained.</p>



<h5 class="wp-block-heading"><strong>Example &#8211; 1:&nbsp;Preparation of Ethyl fluoride (Fluoroethane) from ethyl chloride (Chloroethane):</strong></h5>



<p class="has-text-align-center">C<sub>2</sub>H<sub>5</sub>Cl&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; +&nbsp;&nbsp;&nbsp;&nbsp; AgF&nbsp; &nbsp; →&nbsp; C<sub>2</sub>H<sub>5</sub>F&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; +&nbsp;&nbsp; AgCl</p>



<p class="has-text-align-center">Ethyl chloride&nbsp;&nbsp; silver fluoride&nbsp; &nbsp;Ethyl fluoride&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; silver chloride</p>



<h5 class="wp-block-heading"><strong>Example &#8211; 2:&nbsp;Preparation of Methyl fluoride (Fluoromethane) from methyl bromide (Bromoethane):</strong></h5>



<p class="has-text-align-center">2&nbsp; CH<sub>3</sub>Br&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; +&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hg<sub>2</sub>F<sub>2</sub> &nbsp; &nbsp; →&nbsp; &nbsp; &nbsp; &nbsp;2 CH<sub>3</sub>F&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; +&nbsp;&nbsp; Hg<sub>2</sub>Br<sub>2</sub></p>



<p class="has-text-align-center">Methyl bromide Mercurous fluoride  Methyl fluoride  Mercurous bromide</p>



<p class="has-text-align-center"><strong>For replacement of two or three halogens CoF<sub>3</sub>, SbF<sub>3</sub> are used</strong></p>



<h5 class="wp-block-heading"><strong>Example &#8211; 3</strong></h5>



<div class="wp-block-image"><figure class="aligncenter size-large is-resized"><img fetchpriority="high" decoding="async" src="https://thefactfactor.com/wp-content/uploads/2020/11/Halide-Exchange-Method-02.png" alt="Halide Exchange Method" class="wp-image-15593" width="548" height="99" srcset="https://thefactfactor.com/wp-content/uploads/2020/11/Halide-Exchange-Method-02.png 511w, https://thefactfactor.com/wp-content/uploads/2020/11/Halide-Exchange-Method-02-300x54.png 300w" sizes="(max-width: 548px) 100vw, 548px" /></figure></div>



<p class="has-accent-color has-text-color has-large-font-size"><strong>Preparation of Alkyl bromides from silver salt of fatty acid (Borodine Hunsdiecker Reaction)</strong></p>



<h5 class="wp-block-heading"><strong>General Reaction:</strong></h5>



<p>When silver salt of fatty acid is refluxed with bromine in CCl4, alkyl bromide is obtained.</p>



<p class="has-text-align-center">RCOOAg    +    Br<sub>2</sub>     <img loading="lazy" decoding="async" width="78" height="34" align="middle" class="wp-image-15594" style="width: 78px;" src="https://thefactfactor.com/wp-content/uploads/2020/11/Halide-Exchange-Method-03.png" alt="">   RBr  +   CO<sub>2</sub> +  AgBr</p>



<p class="has-text-align-center">Silver salt of fatty acid   bromine    alkyl bromide   silver bromide</p>



<h5 class="wp-block-heading"><strong>Example -1: Preparation of Methyl Bromide (Bromomethane) from silver acetate:</strong></h5>



<p class="has-text-align-center">CH<sub>3</sub>COOAg    +    Br<sub>2</sub>     <img loading="lazy" decoding="async" width="78" height="34" align="middle" class="wp-image-15594" style="width: 78px;" src="https://thefactfactor.com/wp-content/uploads/2020/11/Halide-Exchange-Method-03.png" alt="">   CH<sub>3</sub>Br  +   CO<sub>2</sub> +  AgBr</p>



<p class="has-text-align-center">Silver acetate  bromine           methyl bromide  silver bromide</p>



<h5 class="wp-block-heading"><strong>Example -2: Preparation of Ethyl Bromide (Brommethane) from silver propionate:</strong></h5>



<p class="has-text-align-center">C<sub>2</sub>H<sub>5</sub>COOAg    +    Br<sub>2</sub>     <img loading="lazy" decoding="async" width="78" height="34" align="middle" class="wp-image-15594" style="width: 78px;" src="https://thefactfactor.com/wp-content/uploads/2020/11/Halide-Exchange-Method-03.png" alt="">   C<sub>2</sub>H<sub>5</sub>Br  +   CO<sub>2</sub> +  AgBr</p>



<p class="has-text-align-center">Silver propionate    bromine          ethyl bromide    silver bromide</p>



<h5 class="wp-block-heading"><strong>Note:</strong></h5>



<p>Chloroalkanes can be obtained by this method but yield is very low. Iodoalkanes can not be obtained by this method because iodine forms easter with  silver salt of fatty acid.</p>



<h5 class="wp-block-heading"><strong>Science > <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/" target="_blank">Chemistry</a> > Organic Chemistry > <a rel="noreferrer noopener" href="https://thefactfactor.com/chemistry/halogen-derivatives-of-alkanes/" target="_blank">Halogen Derivatives of Alkanes</a> > Preparation of Alkyl Halides by Halide Exchange Method</strong></h5>
<p>The post <a href="https://thefactfactor.com/facts/pure_science/chemistry/organic-chemistry/preparation-of-alkyl-halides-by-halide-exchange-method/15590/">Preparation of Alkyl Halides by Halide Exchange Method</a> appeared first on <a href="https://thefactfactor.com">The Fact Factor</a>.</p>
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