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            <Attribute name="description">In this video we look at how we can convert vegetable oils to alkanes via Kolbe&#39;s electrolysis</Attribute>
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            <video:title>Kolbe&#39;s Electrolyis</video:title>
            <video:description>In this video we look at how we can convert vegetable oils to alkanes via Kolbe&#39;s electrolysis</video:description>
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            <Attribute name="description">Kolbe&#39;s electrolysis is a free radical reaction that is widely used in the preparation of symmetrical alkanes from carboxylic acids. This electrolysis process results in decarboxylative dimerisation, ie., carbon dioxide gets eliminated and the alkyl free radical dimerises to form the final symmetrical alkane. </Attribute>
            <Attribute name="author">Revathi</Attribute>
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        <loc>https://www.khanacademy.org/science/organic-chemistry-essentials/x1918b84b5bb1f2e6:free-radical-reactions/x1918b84b5bb1f2e6:halogenation-of-alkanes/v/chlorination-of-propane</loc>
        
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        <lastmod>2023-04-06T06:20:22.223577746Z</lastmod>
        
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            <Attribute name="description">This video talks about the chlorination of an alkane.</Attribute>
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            <video:description>This video talks about the chlorination of an alkane.</video:description>
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    <url>
        <loc>https://www.khanacademy.org/science/organic-chemistry-essentials/x1918b84b5bb1f2e6:free-radical-reactions/x1918b84b5bb1f2e6:halogenation-of-alkanes/e/halogenation-of-alkanes</loc>
        
        <xhtml:link rel="alternate" hreflang="en"
                    href="https://www.khanacademy.org/science/organic-chemistry-essentials/x1918b84b5bb1f2e6:free-radical-reactions/x1918b84b5bb1f2e6:halogenation-of-alkanes/e/halogenation-of-alkanes" />
        
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        <lastmod>2026-04-08T01:15:04.085520103Z</lastmod>
        
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            <Attribute name="description">We will explore more on the free radical halogenation of alkanes such as the selectivity of chlorination vs bromination, what major products are obtained in each of these and what factors affect their formation etc. </Attribute>
            <Attribute name="author">Revathi</Attribute>
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        <loc>https://www.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkene-reactions-tutorial/v/halogenation</loc>
        
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                    href="https://cs.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkene-reactions-tutorial/v/halogenation" />
        
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                    href="https://www.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkene-reactions-tutorial/v/halogenation" />
        
        <xhtml:link rel="alternate" hreflang="es"
                    href="https://es.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkene-reactions-tutorial/v/halogenation" />
        
        <xhtml:link rel="alternate" hreflang="fr"
                    href="https://fr.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkene-reactions-tutorial/v/halogenation" />
        
        <xhtml:link rel="alternate" hreflang="hi"
                    href="https://hi.khanacademy.org/science/up-class-11-chemistry/xa8e73391a9c6d31a:hydrocarbons/xa8e73391a9c6d31a:chemical-properties-of-alkenes/v/halogenation" />
        
        <xhtml:link rel="alternate" hreflang="ka"
                    href="https://ka.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkene-reactions-tutorial/v/halogenation" />
        
        <xhtml:link rel="alternate" hreflang="pl"
                    href="https://pl.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkene-reactions-tutorial/v/halogenation" />
        
        <xhtml:link rel="alternate" hreflang="pt"
                    href="https://pt.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkene-reactions-tutorial/v/halogenation" />
        
        <xhtml:link rel="alternate" hreflang="uz"
                    href="https://uz.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkene-reactions-tutorial/v/halogenation" />
        
        <lastmod>2021-03-22T03:07:31Z</lastmod>
        
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            <Attribute name="title">Alkene halogenation</Attribute>
            <Attribute name="description">Halogenation is a reaction that occurs when one or more halogens are added to a substance. Halogens comprise the seventh column in the periodic table and include fluorine, chlorine, bromine, iodine, and astatine. The resulting product of a halogenation reaction is known as a halogenated compound.</Attribute>
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            <video:title>Alkene halogenation</video:title>
            <video:description>Halogenation is a reaction that occurs when one or more halogens are added to a substance. Halogens comprise the seventh column in the periodic table and include fluorine, chlorine, bromine, iodine, and astatine. The resulting product of a halogenation reaction is known as a halogenated compound.</video:description>
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    </url>
    
    <url>
        <loc>https://www.khanacademy.org/science/telangana-class-12-chemistry/x50160c6c142df488:haloalkanes-and-haloarenees/x50160c6c142df488:preparation-of-haloalkanes/e/electrophilic-addition-of-halogens-to-alkenes</loc>
        
        <xhtml:link rel="alternate" hreflang="en"
                    href="https://www.khanacademy.org/science/telangana-class-12-chemistry/x50160c6c142df488:haloalkanes-and-haloarenees/x50160c6c142df488:preparation-of-haloalkanes/e/electrophilic-addition-of-halogens-to-alkenes" />
        
        <xhtml:link rel="alternate" hreflang="hi"
                    href="https://hi.khanacademy.org/science/up-class-11-chemistry/xa8e73391a9c6d31a:hydrocarbons/xa8e73391a9c6d31a:chemical-properties-of-alkenes/e/electrophilic-addition-of-halogens-to-alkenes" />
        
        <lastmod>2026-04-07T23:55:07.30621384Z</lastmod>
        
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            <Attribute name="description">Through this exercise, we will test and further our understanding of the addition of halogens to alkenes and the mechanism behind it. </Attribute>
            <Attribute name="author">Revathi</Attribute>
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    <url>
        <loc>https://www.khanacademy.org/science/ka-chemistry-grade-11/x7b9df4d3282049b3:in-in-hydrocarbons/x7b9df4d3282049b3:in-in-alkenes-properties/e/peroxide-effect</loc>
        
        <xhtml:link rel="alternate" hreflang="en"
                    href="https://www.khanacademy.org/science/ka-chemistry-grade-11/x7b9df4d3282049b3:in-in-hydrocarbons/x7b9df4d3282049b3:in-in-alkenes-properties/e/peroxide-effect" />
        
        <xhtml:link rel="alternate" hreflang="hi"
                    href="https://hi.khanacademy.org/science/up-class-11-chemistry/xa8e73391a9c6d31a:hydrocarbons/xa8e73391a9c6d31a:chemical-properties-of-alkenes/e/peroxide-effect" />
        
        <lastmod>2026-04-07T23:55:07.30621384Z</lastmod>
        
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            <Attribute name="title">Peroxide effect</Attribute>
            <Attribute name="description">We are familiar with converting an alkene into an alkyl halide of markovnikov&#39;s orientation based on the stability of the intermediate carbocation. Here, we will explore how to obtain an alkyl halide from an alkene with an antimarkovnikov&#39;s orientation but something that happens specifically for HBr alone (and not HCl and HI). We will see that, in the presence of peroxides, bromide ion adds to the less substituted end of the double bond (in general, depending on the stability of the intermediate free radical). </Attribute>
            <Attribute name="author">Revathi</Attribute>
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    </url>
    
    <url>
        <loc>https://www.khanacademy.org/science/organic-chemistry/alkenes-alkynes/naming-preparation-alkynes/v/preparation-of-alkynes</loc>
        
        <xhtml:link rel="alternate" hreflang="az"
                    href="https://az.khanacademy.org/science/organic-chemistry/alkenes-alkynes/naming-preparation-alkynes/v/preparation-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="bg"
                    href="https://bg.khanacademy.org/science/organic-chemistry/alkenes-alkynes/naming-preparation-alkynes/v/preparation-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="cs"
                    href="https://cs.khanacademy.org/science/organic-chemistry/alkenes-alkynes/naming-preparation-alkynes/v/preparation-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="en"
                    href="https://www.khanacademy.org/science/organic-chemistry/alkenes-alkynes/naming-preparation-alkynes/v/preparation-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="es"
                    href="https://es.khanacademy.org/science/organic-chemistry/alkenes-alkynes/naming-preparation-alkynes/v/preparation-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="fr"
                    href="https://fr.khanacademy.org/science/organic-chemistry/alkenes-alkynes/naming-preparation-alkynes/v/preparation-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="hi"
                    href="https://hi.khanacademy.org/science/up-class-11-chemistry/xa8e73391a9c6d31a:hydrocarbons/xa8e73391a9c6d31a:preparation-of-alkynes/v/preparation-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="ka"
                    href="https://ka.khanacademy.org/science/organic-chemistry/alkenes-alkynes/naming-preparation-alkynes/v/preparation-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="pt"
                    href="https://pt.khanacademy.org/science/organic-chemistry/alkenes-alkynes/naming-preparation-alkynes/v/preparation-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="tr"
                    href="https://tr.khanacademy.org/science/12-sinif-kimya/xbe473057f0ca4813:3-unite-organik-bilesikler/xbe473057f0ca4813:hidrokarbonlar/v/preparation-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="uz"
                    href="https://uz.khanacademy.org/science/organic-chemistry/alkenes-alkynes/naming-preparation-alkynes/v/preparation-of-alkynes" />
        
        <lastmod>2021-03-22T03:07:30Z</lastmod>
        
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            <Attribute name="title">Preparation of alkynes</Attribute>
            <Attribute name="description">Note that if a terminal alkyne is produced, the strong base will deprotonate the alkyne to form an alkynide anion. A proton source (like H2O) must be added to regenerate the terminal alkyne.</Attribute>
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            <video:description>Note that if a terminal alkyne is produced, the strong base will deprotonate the alkyne to form an alkynide anion. A proton source (like H2O) must be added to regenerate the terminal alkyne.</video:description>
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    </url>
    
    <url>
        <loc>https://www.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes</loc>
        
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                    href="https://az.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
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                    href="https://bg.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="cs"
                    href="https://cs.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="en"
                    href="https://www.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="es"
                    href="https://es.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="fr"
                    href="https://fr.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="hi"
                    href="https://hi.khanacademy.org/science/up-class-11-chemistry/xa8e73391a9c6d31a:hydrocarbons/xa8e73391a9c6d31a:chemical-properties-of-alkynes/v/hydration-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="ka"
                    href="https://ka.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="pl"
                    href="https://pl.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="pt"
                    href="https://pt.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="tr"
                    href="https://tr.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
        <xhtml:link rel="alternate" hreflang="uz"
                    href="https://uz.khanacademy.org/science/organic-chemistry/alkenes-alkynes/alkyne-reactions/v/hydration-of-alkynes" />
        
        <lastmod>2021-03-22T03:07:31Z</lastmod>
        
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            <Attribute name="description">Reaction between a terminal alkyne, a strong acid, and mercury (II) sulfate. Using Mark&#39;s rule to determine the regiochemistry of addition, and the mechanism of acid-catalyzed tautomerization. </Attribute>
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            <video:title>Hydration of alkynes</video:title>
            <video:description>Reaction between a terminal alkyne, a strong acid, and mercury (II) sulfate. Using Mark&#39;s rule to determine the regiochemistry of addition, and the mechanism of acid-catalyzed tautomerization. </video:description>
            <video:player_loc>https://cdn.kastatic.org/ka-youtube-converted/AE1pkp-_cKE.mp4/AE1pkp-_cKE.mp4</video:player_loc>
            <video:duration>477</video:duration>
            <video:category>Hydrocarbons</video:category>
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    </url>
    
    <url>
        <loc>https://www.khanacademy.org/science/ka-chemistry-grade-11/x7b9df4d3282049b3:in-in-hydrocarbons/x7b9df4d3282049b3:in-in-alkynes-properties/e/hydrohalogenation-of-alkynes</loc>
        
        <xhtml:link rel="alternate" hreflang="en"
                    href="https://www.khanacademy.org/science/ka-chemistry-grade-11/x7b9df4d3282049b3:in-in-hydrocarbons/x7b9df4d3282049b3:in-in-alkynes-properties/e/hydrohalogenation-of-alkynes" />
        
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        <lastmod>2026-04-07T23:55:07.30621384Z</lastmod>
        
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