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      <title>Chemistry 4.4 by Holly Jones</title>
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      <description>Made with whimsy</description>
      <language>en-us</language>
      <pubDate>2019-01-30 12:12:16 UTC</pubDate>
      <lastBuildDate>2024-12-18 19:28:25 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>Fehling&#39;s Solution</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/upvg1nqvqhib/wish/325795239</link>
         <description><![CDATA[<div>A red/orange precipitate forms when Fehling's solution is warmed with an aldehyde but not with a ketone.<br>Solution contains: Cu<sup>2+<br></sup>Cu<sup>2+</sup> + e<sup>- </sup>--&gt; Cu<sup>+ <br></sup>Cu<sub>2</sub>O (red/orange ppt)  is formed from Cu<sup>+</sup> ions</div>]]></description>
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         <pubDate>2019-01-30 12:12:28 UTC</pubDate>
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         <title>Fehling&#39;s and Tollens&#39; Test</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/upvg1nqvqhib/wish/325795240</link>
         <description><![CDATA[<div>Two reagents may be used for testing:<br>1) Tollens' reagent. containing the complex ion [Ag(NH<sub>3</sub>)<sub>2</sub>]<sup>+<br></sup>2) Fehling's solution, containing Cu<sup>2+</sup> ions</div>]]></description>
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         <pubDate>2019-01-30 12:12:28 UTC</pubDate>
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         <title></title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/upvg1nqvqhib/wish/325795241</link>
         <description><![CDATA[<div>Ketones resist oxidation. <br>Aldehydes are easily oxidised.</div>]]></description>
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         <pubDate>2019-01-30 12:12:28 UTC</pubDate>
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         <title>Test for primary and secondary alcohols</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/upvg1nqvqhib/wish/325795242</link>
         <description><![CDATA[<div>Reagents: Potassium dichromate (VI) solution (K<sub>2</sub>Cr<sub>2</sub>O<sub>7(aq)</sub>)<br>Dilute Sufuric acid (H<sub>2</sub>SO<sub>4(aq)</sub> )<br>Observations: Colour change from orange to green</div>]]></description>
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         <pubDate>2019-01-30 12:12:28 UTC</pubDate>
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         <title>Reduction</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/upvg1nqvqhib/wish/325795243</link>
         <description><![CDATA[<div>The removal of oxygen atoms or the addition of hydrogen atoms</div>]]></description>
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         <pubDate>2019-01-30 12:12:28 UTC</pubDate>
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         <title>Oxidation</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/upvg1nqvqhib/wish/325795244</link>
         <description><![CDATA[<div>The addition of oxygen atoms or the removal or hydrogen atoms</div>]]></description>
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         <pubDate>2019-01-30 12:12:28 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/upvg1nqvqhib/wish/325795244</guid>
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         <title>Oxidation of alcohol</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/upvg1nqvqhib/wish/325795245</link>
         <description><![CDATA[<div>Primary alcohol --&gt; Aldehyde --&gt; Carboxylic Acid</div><ul><li>Extract the aldehyde using distillation </li><li>Extract carboxylic acid using reflux </li></ul><div>Secondary alcohol --&gt; Ketone<br>Needs H<sub>2</sub>SO<sub>4(aq)</sub> and K<sub>2</sub>Cr<sub>2</sub>O<sub>7(aq)</sub></div>]]></description>
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         <pubDate>2019-01-30 12:12:28 UTC</pubDate>
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         <title>Aldehydes and Keytones</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/upvg1nqvqhib/wish/325795246</link>
         <description><![CDATA[]]></description>
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         <pubDate>2019-01-30 12:12:28 UTC</pubDate>
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