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      <title>CHEMISTRY PROYECT by Diego Velasquez</title>
      <link>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy</link>
      <description></description>
      <language>en-us</language>
      <pubDate>2022-06-03 18:37:47 UTC</pubDate>
      <lastBuildDate>2025-12-09 12:55:32 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>DEFINITION</title>
         <author>diegoalessandrov</author>
         <link>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210476345</link>
         <description><![CDATA[<div>an alkyne is <strong>an unsaturated hydrocarbon containing at least one carbon-carbon triple bond</strong>. The alkynes are unsaturated hydrocarbons that contain one triple bond, the general formula of alkynes C<sub>n</sub>H<sub>2n+2</sub> and the triple bond is known as the 'acetylenic bond'. Many alkynes have been found in nature.</div>]]></description>
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         <pubDate>2022-06-03 18:38:52 UTC</pubDate>
         <guid>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210476345</guid>
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      <item>
         <title>ALKYNES STRUCTURE</title>
         <author>diegoalessandrov</author>
         <link>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210483282</link>
         <description><![CDATA[]]></description>
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         <pubDate>2022-06-03 18:49:10 UTC</pubDate>
         <guid>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210483282</guid>
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         <title>WHERE CAN ALKYNES BE USED</title>
         <author>diegoalessandrov</author>
         <link>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210485287</link>
         <description><![CDATA[<ul><li>The most common use of Ethyne is for making organic compounds like ethanol, ethanoic acid, acrylic acid, etc.</li><li>It is also used for making polymers and its beginning materials. ...</li><li>Ethyne is used for preparing many organic solvents.</li><li>Alkynes are commonly used to artificially ripe fruits.</li></ul><div><br></div>]]></description>
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         <pubDate>2022-06-03 18:52:22 UTC</pubDate>
         <guid>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210485287</guid>
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      <item>
         <title>PHYSICAL PROPERTIES</title>
         <author>diegoalessandrov</author>
         <link>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210487782</link>
         <description><![CDATA[<div>Alkynes are nonpolar, unsaturated hydrocarbons with physical properties similar to alkanes and alkenes. Alkynes <strong>dissolve in organic solvents, have slight solubility in polar solvents, and are insoluble in water</strong>. Compared to alkanes and alkenes, alkynes have slightly higher boiling points.</div>]]></description>
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         <pubDate>2022-06-03 18:56:23 UTC</pubDate>
         <guid>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210487782</guid>
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      <item>
         <title>INTERESTING FACTS OF ALKYLNE</title>
         <author>diegoalessandrov</author>
         <link>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210490252</link>
         <description><![CDATA[<div>Alkynes and compounds containing alkynes in their chemical structures are <strong>useful in various industries</strong>. For instance, in the fuel industry and plastics industry, alkynes like propyne and acetylene are used as starting materials in manufacturing plastic products.</div>]]></description>
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         <pubDate>2022-06-03 19:00:01 UTC</pubDate>
         <guid>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210490252</guid>
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      <item>
         <title>ALKYNES REACTION</title>
         <author>diegoalessandrov</author>
         <link>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210494106</link>
         <description><![CDATA[<div>he principal reaction of the alkynes is <strong>addition across the triple bond to form alkanes</strong>. These addition reactions are analogous to those of the alkenes. Hydrogenation. Alkynes undergo catalytic hydrogenation with the same catalysts used in alkene hydrogenation: platinum, palladium, nickel, and rhodium.</div>]]></description>
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         <pubDate>2022-06-03 19:05:50 UTC</pubDate>
         <guid>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210494106</guid>
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         <title>REFERENCES</title>
         <author>diegoalessandrov</author>
         <link>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210495409</link>
         <description><![CDATA[<div>sciencedirect.com<br>cameochemicals.com<br>britannica.com</div>]]></description>
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         <pubDate>2022-06-03 19:08:14 UTC</pubDate>
         <guid>https://padlet.com/diegoalessandrov/ymr87htbu1shdjhy/wish/2210495409</guid>
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