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      <title>The Chemistry Of Ketones by Chris Navas</title>
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      <description></description>
      <language>en-us</language>
      <pubDate>2022-05-19 01:17:10 UTC</pubDate>
      <lastBuildDate>2022-05-19 02:12:39 UTC</lastBuildDate>
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         <author>cckicame</author>
         <link>https://padlet.com/cckicame/iudtn64t00o2d0w2/wish/2190414663</link>
         <description><![CDATA[<div>KETONES <br><br><strong>ketone, any of a class of organic compounds characterized by the presence of a carbonyl group in which the carbon atom is covalently bonded to an oxygen atom. The remaining two bonds are to other carbon atoms or hydrocarbon radicals (R): Ketone compounds have important physiological properties</strong></div>]]></description>
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         <pubDate>2022-05-19 01:29:52 UTC</pubDate>
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         <title></title>
         <author>cckicame</author>
         <link>https://padlet.com/cckicame/iudtn64t00o2d0w2/wish/2190422730</link>
         <description><![CDATA[<div>STRUCTURES<br><strong>In chemistry, a ketone /ˈkiːtoʊn/ is a functional group with the structure R</strong><strong><sub>2</sub></strong><strong>C=O, where R can be a variety of carbon-containing substituents. Ketones contain a carbonyl group (a carbon-oxygen double bond). The simplest ketone is acetone (R = R' = methyl), with the formula CH</strong><strong><sub>3</sub></strong><strong>C(O)CH</strong><strong><sub>3</sub></strong><strong>.</strong></div>]]></description>
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         <pubDate>2022-05-19 01:35:42 UTC</pubDate>
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         <title></title>
         <author>cckicame</author>
         <link>https://padlet.com/cckicame/iudtn64t00o2d0w2/wish/2190440229</link>
         <description><![CDATA[<div>STRUCTURES<br><br>testosterone<br>muscone<br>vainilil&nbsp;<br>citral<br>cortisone<br><br></div>]]></description>
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         <pubDate>2022-05-19 01:48:28 UTC</pubDate>
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         <title></title>
         <author>cckicame</author>
         <link>https://padlet.com/cckicame/iudtn64t00o2d0w2/wish/2190473177</link>
         <description><![CDATA[<div><sub>REACTIONS<br><br></sub><strong><sub>&nbsp;ketones undergo a variety of reactions that lead to many different products. The most common reactions are nucelophilic adition reactions, which lead to the formation of alcohols, alkenes, diols, cyanohydrins (RCH(OH)C&amp;tbond;N), and imines R 2C&amp;dbond;NR), to mention a few representative examples</sub></strong></div>]]></description>
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         <pubDate>2022-05-19 02:07:15 UTC</pubDate>
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         <title></title>
         <author>cckicame</author>
         <link>https://padlet.com/cckicame/iudtn64t00o2d0w2/wish/2190475481</link>
         <description><![CDATA[<div>USES<br><strong>They are most widely used as solvents, especially in industries manufacturing explosives, lacquers, paints, and textiles. Ketones are also used in tanning, as preservatives, and in hydraulic fluids. The most important ketone is acetone (CH</strong><strong><sub>3</sub></strong><strong>COCH</strong><strong><sub>3</sub></strong><strong>), a liquid with a sweetish odour.</strong></div><div><br><br></div>]]></description>
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         <pubDate>2022-05-19 02:08:42 UTC</pubDate>
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         <title></title>
         <author>cckicame</author>
         <link>https://padlet.com/cckicame/iudtn64t00o2d0w2/wish/2190479219</link>
         <description><![CDATA[<div>https://www.britannica.com/science/resin</div>]]></description>
         <enclosure url="https://www.britannica.com/science/resin" />
         <pubDate>2022-05-19 02:11:05 UTC</pubDate>
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         <title></title>
         <author>cckicame</author>
         <link>https://padlet.com/cckicame/iudtn64t00o2d0w2/wish/2190480378</link>
         <description><![CDATA[<div>https://en.wikipedia.org/wiki/Ketone#:~:text=In%20chemistry%2C%20a%20ketone%20%2F%CB%88,C(O)CH3.</div>]]></description>
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         <pubDate>2022-05-19 02:11:50 UTC</pubDate>
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         <title></title>
         <author>cckicame</author>
         <link>https://padlet.com/cckicame/iudtn64t00o2d0w2/wish/2190481629</link>
         <description><![CDATA[<div>https://www.cliffsnotes.com/study-guides/chemistry/organic-chemistry-ii/aldehydes-and-ketones/reactions-of-aldehydes-and-ketones#:~:text=Aldehydes%20and%20ketones%20undergo%20a,mention%20a%20few%20representative%20examples.</div>]]></description>
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         <pubDate>2022-05-19 02:12:39 UTC</pubDate>
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