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      <title>Chemistry 2.5 by Holly Jones</title>
      <link>https://padlet.com/hol_cjones/zquys1x34w9s</link>
      <description>Made with eyes on the prize</description>
      <language>en-us</language>
      <pubDate>2019-01-30 12:12:16 UTC</pubDate>
      <lastBuildDate>2025-12-02 05:25:21 UTC</lastBuildDate>
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      <item>
         <title>Mechanism 1: Radical Substitution</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795095</link>
         <description><![CDATA[<div>Halogenation<br>Example - Photochlorination of Chlorine<br>Stage 1: Initiation - Start the mechanism by making radicals<br>Stage 2: Propahation- Continue the mechanism&nbsp;<br>In general: Radical + Molecule —&gt; New molecule + New Radical<br>Stage 3: Termination - Remove radicals and stop</div>]]></description>
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         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795095</guid>
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         <title>Saturated Hydrocarbons</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795096</link>
         <description><![CDATA[<div>A compound of hydrogen and carbon containing no C to C multiple bonds.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795096</guid>
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         <title>Carbocations </title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795097</link>
         <description><![CDATA[<div>Order of Stability <br>Most: Tertairy carbocation<br>            Secondary carbocation<br>Least: Primary carbocation</div>]]></description>
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         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795097</guid>
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      <item>
         <title>Addition Polymerisation </title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795098</link>
         <description><![CDATA[<div>Double bonds are used to join monomers and only one product forms</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795098</guid>
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      <item>
         <title>Hydrogenation</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795099</link>
         <description><![CDATA[<div>Catalytic Hydrogenation<br>Hydrogenation of Ethane<br>Reagent : Hydrogen<br>Catalyst: Nickel (Ni)<br>Conditions: 140 degrees Celsius temperature <br>C<sub>2</sub>H<sub>4</sub> + H<sub>2</sub> —&gt; C<sub>2</sub>H<sub>6</sub><br>Heterogeneous catalyst: Catalyst and reactants are in different states<br>Uses - Liquid vegetable oils (polyunsaturates- has multiple bonds) can be made saturated by adding hydrogen. This hardens the oil to make margarine.<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795099</guid>
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      <item>
         <title>Unsaturated Hydrocarbon</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795100</link>
         <description><![CDATA[<div>A compound of hydrogen and carbon containing C to C multiple bonds</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795100</guid>
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      <item>
         <title>Addition of HBr to Propene</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795101</link>
         <description><![CDATA[]]></description>
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         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795101</guid>
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      <item>
         <title>Carbocation</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795102</link>
         <description><![CDATA[<div>A positively charge carbon-containing ion.</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795102</guid>
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      <item>
         <title>Test For Alkenes</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795103</link>
         <description><![CDATA[<div>Reagent: Bromine Water<br>Observation: Colour change from orange/yellow to colourless<br>OR<br>Reagent: Acidified potassium manganate (VII)<br>Observation: Colour change from purple to colourless</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795103</guid>
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      <item>
         <title>Mechanism 2: Electrophilic Addition </title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795104</link>
         <description><![CDATA[]]></description>
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         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795104</guid>
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      <item>
         <title>Bonding in Alkanes</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795105</link>
         <description><![CDATA[]]></description>
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         <pubDate>2019-01-30 12:12:22 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795105</guid>
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      <item>
         <title>Benefits and Drawbacks of using fossil fules</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795107</link>
         <description><![CDATA[<div>Benefits</div><ul><li>More reliable- eco friendly methods, eg. wind, solar, aren't alwas available</li><li>Produce lots of energy</li><li>Provides jobs- in power plants and extracting fuel </li><li>Many forms of fossil fuels- can be used for different things</li></ul><div>Drawbacks</div><ul><li>Non-renewable- will run out eventually</li><li>When burnt, they release CO (carbon monoxide) which is toxic to humans</li><li>Release CO<sub>2</sub> (carbon dioxide) which has a negative impact on global warming.</li><li>Disrupts the natural environment to access fuels</li><li>Expensive to get materials and transfer them into energy - powerplants</li><li>Can create acid rain which can damage buildings</li></ul>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:23 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795107</guid>
      </item>
      <item>
         <title>Complete/Incomplete combustion</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795108</link>
         <description><![CDATA[<ul><li>If there is enough oxygen we get complete combustion with carbon dioxide and water as products</li><li>If there is insufficient oxygen, incomplete combustion occurs and carbon monoxide is made.</li></ul>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:23 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795108</guid>
      </item>
      <item>
         <title>Bonding in Alkenes</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795109</link>
         <description><![CDATA[]]></description>
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         <pubDate>2019-01-30 12:12:23 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795109</guid>
      </item>
      <item>
         <title>Alkene Reactivity </title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795110</link>
         <description><![CDATA[<div>Alkenes are much more reactive than alkanes due to the C=C bond in the alkenes being a region of high electron density</div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:23 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795110</guid>
      </item>
      <item>
         <title>E-Z Isomerism </title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795111</link>
         <description><![CDATA[<div>Occurs in alkenes and substituted alkenes due to restricted rotation around the C=C double bond<br><br>Identifying E or Z<br>Look at the atoms/groups at earthier end of the double bond<br>Rank the atoms/groups, taking. The atoms with higher atomic numbers as the most important<br>Define the isomer as either<br>Z isomer - higher priority atoms/groups are on the same side of the double bond<br>E isomer - Higher priority atoms/ groups are on opposite sides of the double bond.</div>]]></description>
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         <pubDate>2019-01-30 12:12:23 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795111</guid>
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      <item>
         <title>Polymers</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/zquys1x34w9s/wish/325795112</link>
         <description><![CDATA[<ul><li>Example- Plastics</li><li>A very large molecule made up of many repeating units or blocks</li><li>We make polymers by joining up (polymerisation) hundreds or thousands of small reactive molecules called monomers.</li></ul><div>Ethene  —&gt; polyethene (polythene) <br>Conditions : 2000atm, 200 degrees Celsius, trace of oxygen</div>]]></description>
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         <pubDate>2019-01-30 12:12:23 UTC</pubDate>
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