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      <title>Chemistry 2.7 by Holly Jones</title>
      <link>https://padlet.com/hol_cjones/gmfcnslz3ql7</link>
      <description>Made with a taste for adventure</description>
      <language>en-us</language>
      <pubDate>2019-01-30 12:12:16 UTC</pubDate>
      <lastBuildDate>2025-04-25 16:12:21 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>Making an Ester</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795154</link>
         <description><![CDATA[<div>1) Water bath - 250ml beaker ~50°C&nbsp;<br>2) Pear Flask-</div><ul><li>25ml CH<sub>3</sub>COOH</li><li>10ml C<sub>2</sub>H<sub>5</sub>OH</li><li>10 drops H<sub>2</sub>SO<sub>4</sub></li><li>~5 anti-bumping granules</li></ul><div>3) Put into water bath for 15 mins</div>]]></description>
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         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795154</guid>
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      <item>
         <title>Testing for alcohols - traffic light test</title>
         <author>317683</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795155</link>
         <description><![CDATA[<div>Reagents: Potassium dichromate(VI) &amp; dilute sulfuric acid<br>Observations: Colour change from orange to green<br><br>Cr<sub>2</sub>O<sub>7</sub><sup>2- </sup>(orange) ions change to Cr<sup>3+</sup> (green) ions.</div>]]></description>
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         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795155</guid>
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         <title>Alcohol Oxidation</title>
         <author>317683</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795156</link>
         <description><![CDATA[<ul><li>Oxidation is the addition of oxygen atoms or removal of hydrogen atoms.</li><li>Reduction is the removal of oxygen atoms or addition of hydrogen atoms.</li></ul><div>ethanol(primary) + [O] (oxidising agent) --&gt; ethanal(AL - aldehyde)<br>C<sub>2</sub>H<sub>5</sub>OH + [O] --&gt; CH<sub>3</sub>CHO + H<sub>2</sub>O <br>ethanal + [O] --&gt; ethnic acid(carboxylic acid)<br>CH<sub>3</sub>CHO + [O] --&gt; CH<sub>3</sub>COOH<br>--&gt; along the arrow - H<sup>+</sup>(aq) &amp; K<sub>2</sub>Cr<sub>2</sub>O<sub>7<br><br></sub>Primary alcohol --&gt; Aldehyde --&gt; Carboxylic acid<br>Secondary alcohol --&gt; Ketone<br><br>We can use dilute Potassium dichromate(VI) solution acidified with dilute sulfuric acid.<br><br></div>]]></description>
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         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795156</guid>
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         <title>Alcohol Dehydration</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795157</link>
         <description><![CDATA[<div>C<sub>2</sub>H<sub>5</sub>OH --&gt; C<sub>2</sub>H<sub>4</sub> + H<sub>2</sub>O<br>Catalyst = Concentrated H<sub>2</sub>SO<sub>4</sub><br>Example<br>CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH --&gt; CH<sub>3</sub>CHCH<sub>2</sub> + H<sub>2</sub>O<br>Propan-1-ol --&gt; Propene + Water</div>]]></description>
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         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795157</guid>
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         <title>Testing for carboxylic acids</title>
         <author>317683</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795158</link>
         <description><![CDATA[<div>Reagent: Sodium hydrogen carbonate(NaHCO<sub>3</sub>) or sodium carbonate(Na<sub>2</sub>CO<sub>3</sub>) <br>Observation: effervescence (CO<sub>2</sub> produced)</div>]]></description>
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         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795158</guid>
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         <title>Biological route of making ethanol</title>
         <author>317683</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795159</link>
         <description><![CDATA[<div>Photosynthesis: 6CO<sub>2</sub> + 6H<sub>2</sub>O --&gt; C<sub>6</sub>H<sub>12</sub>O<sub>6</sub> + 6O<sub>2</sub><br>Fermentation(yeast): C<sub>6</sub>H<sub>12</sub>O<sub>6</sub> --&gt; 2C<sub>2</sub>H<sub>5</sub>OH + 2CO<sub>2<br></sub>Combustion: C<sub>2</sub>H<sub>5</sub>OH + 3O<sub>2</sub>--&gt; 2CO<sub>2</sub> + 3H<sub>2</sub>O<br><br>Fermentation is an enzyme catalysed reaction, converting sugars to ethanol. YEast is often used.<br>Bio fuels are fuels produced from a biological source. <br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795159</guid>
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      <item>
         <title>Fractional Distillation of Ethanol</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795160</link>
         <description><![CDATA[]]></description>
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         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795160</guid>
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      <item>
         <title>Making Ethanol</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795161</link>
         <description><![CDATA[<div>H<sub>2</sub>C=CH<sub>2(g)</sub> + H<sub>2</sub>0<sub>(g)</sub> <strong>⇌ </strong>C<sub>2</sub>H<sub>5</sub>OH <sub>(g)<br></sub>ΔH = -45kJmol<sup>-1</sup><sub><br></sub>Reactants = Ethene + Steam<br>Product = Ethanol<br>Catalyst = Phosphoric Acid (H<sub>3</sub>PO<sub>4</sub>)<br>Conditions = 300 ºC , 60-70 atm</div><ul><li>Catalyst used to speed up reaction by decreasing the activation energy, therefore allowing more product to be produced</li><li>High pressure used - 2:1 moles of gas therefore PoE shifts —&gt; More product produced because the forward reaction is favoured</li><li>High temperature used - Forward reaction = Exothermic therefore if you cool the reaction the PoE shifts —&gt; and products increase, however the rate decreases. 300ºC is a compromise temperature because its hot enough to give a decent rate but cool enough to let the PoE shifts —&gt;</li></ul>]]></description>
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         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795161</guid>
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      <item>
         <title>Example of an Ester</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795162</link>
         <description><![CDATA[]]></description>
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         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795162</guid>
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      <item>
         <title>Esters </title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795163</link>
         <description><![CDATA[<div>Carboxylic acid + Alcohol <strong>⇌</strong>  Ester + Water<br>Forwards reaction = Esterification<br>Backwards reaction Hydrolysis </div>]]></description>
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         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795163</guid>
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      <item>
         <title>Benefits and Drawbacks of Biofuel</title>
         <author>hol_cjones</author>
         <link>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795165</link>
         <description><![CDATA[<div><strong>Benefits</strong></div><ul><li>Produces less CO<sub>2</sub> than greenhouse gases</li><li>Renewable</li><li>Easy to source- formed from many different sources eg. manure, crops and plants</li><li>Creates jobs as biofuel industry grows</li></ul><div><strong>Drawbacks</strong></div><ul><li>Plants are produced in other countries therefore they have to be transported- transport uses fossil fuels</li><li>May not have suitable conditions to grow plants in the UK</li><li>Ethical issue- using land in poor countries to grow plants for fuel rather than food</li><li>May increase water demand</li><li>May require fertilisers- dangerous to environment</li></ul>]]></description>
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         <pubDate>2019-01-30 12:12:25 UTC</pubDate>
         <guid>https://padlet.com/hol_cjones/gmfcnslz3ql7/wish/325795165</guid>
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