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      <title>Chemistry 4.1 by Holly Jones</title>
      <link>https://padlet.com/hol_cjones/3qvhlzrjxi05</link>
      <description>Made with eyes on the prize</description>
      <language>en-us</language>
      <pubDate>2019-01-30 12:12:16 UTC</pubDate>
      <lastBuildDate>2025-11-02 02:25:57 UTC</lastBuildDate>
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      <item>
         <title>Z- Isomer</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794954</link>
         <description><![CDATA[<div>Bromine is the higher priority group because it has a higher atomic number.<br>The bromine is on THE SAME SIDE of the double bond.</div>]]></description>
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         <pubDate>2019-01-30 12:12:17 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794954</guid>
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      <item>
         <title>Types of Stereoisomerism</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794955</link>
         <description><![CDATA[<ul><li>E-Z Isomerism</li><li>Optical Isomerism</li></ul>]]></description>
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         <pubDate>2019-01-30 12:12:17 UTC</pubDate>
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         <title></title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794956</link>
         <description><![CDATA[<ul><li>Equimolar amounts of each enantiomer in a mixture will form a racemic mixture.</li><li>These mixtures are sometimes also called racemates.</li><li>The (+) and (-) rotations of the polarised light will cancel eachother out.</li><li>Therefore a racemic mixture is not optically active.</li></ul>]]></description>
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         <pubDate>2019-01-30 12:12:17 UTC</pubDate>
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         <title>Enantiomers</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794957</link>
         <description><![CDATA[<div>Enantiomers rotate the plane of polarised light that shines on to them:</div><ul><li>The positive (+) isomer rotated the plane of polarisation clockwise</li><li>The negative (-) isomer rotates the plane of polarisation anticlockwise</li></ul>]]></description>
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         <pubDate>2019-01-30 12:12:17 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794957</guid>
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      <item>
         <title>ENANTIOMERS </title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794958</link>
         <description><![CDATA[<div>Non-superimposable mirror image forms of each other that rotate the plane of polarised light in opposite directions.</div>]]></description>
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         <pubDate>2019-01-30 12:12:17 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794958</guid>
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      <item>
         <title>CHIRAL CENTRE</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794959</link>
         <description><![CDATA[<div>A carbon atom attached to four different atoms or groups.</div>]]></description>
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         <pubDate>2019-01-30 12:12:17 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794959</guid>
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      <item>
         <title>Waves</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794960</link>
         <description><![CDATA[<div>1) Side angle<br>2) End Angle</div>]]></description>
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         <pubDate>2019-01-30 12:12:17 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794960</guid>
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      <item>
         <title>E-Z Isomerism</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794961</link>
         <description><![CDATA[<div>To have E-Z isomerism</div><ul><li>a and b must be different</li><li>c and d must be different </li></ul><div>(Needs 2 different groups)</div>]]></description>
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         <pubDate>2019-01-30 12:12:17 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794961</guid>
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      <item>
         <title></title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794962</link>
         <description><![CDATA[]]></description>
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         <pubDate>2019-01-30 12:12:17 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794962</guid>
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      <item>
         <title>STEREOISOMERISM</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794963</link>
         <description><![CDATA[<div>Occurs when the isomers have the same shortened formula but have a different arrangement of atoms in space.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:18 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794963</guid>
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      <item>
         <title>Stereoisomerism</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794964</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:18 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794964</guid>
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      <item>
         <title>E- Isomer</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794965</link>
         <description><![CDATA[<div>Bromine is the higher priority group because it has a higher atomic number<br>The bromine is on  EITHER SIDE of the double bond.</div>]]></description>
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         <pubDate>2019-01-30 12:12:18 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794965</guid>
      </item>
      <item>
         <title>OPTICAL ISOMERS</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794966</link>
         <description><![CDATA[<div>Isomers that have the same molecular formula and the same structural formula, but have a different effect upon plane polarised light.<br>The isomers are non-superimposable mirror images of each other.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:18 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794966</guid>
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      <item>
         <title>STRUCTURAL ISOMERS</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794967</link>
         <description><![CDATA[<div>Compounds with the same molecular formula but different structural formulas (arrangement of atoms)</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:18 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/3qvhlzrjxi05/wish/325794967</guid>
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