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      <title>Experiment 5: Reactions of Hydroxy Compounds by Nurul Izzaty</title>
      <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1</link>
      <description>Objectives:</description>
      <language>en-us</language>
      <pubDate>2025-01-02 03:44:25 UTC</pubDate>
      <lastBuildDate>2025-08-06 07:53:31 UTC</lastBuildDate>
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         <title>What we have learned</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375071</link>
         <description><![CDATA[]]></description>
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      <item>
         <title>Group 1</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375072</link>
         <description><![CDATA[<p>Hiii we are group 1️⃣☝️! </p>]]></description>
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      <item>
         <title>Team A</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375073</link>
         <description><![CDATA[<p><br></p><ol><li><p>Nurul Athirah binti Ariffin Kamal (MS2417120919)</p></li><li><p>Nurul Izzaty Akhtar binti Syahril Anwar (MS2418122911)</p></li></ol>]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title>Team B</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375075</link>
         <description><![CDATA[<ol><li><p>Leong Zhi Ying (MS2417121685）</p></li><li><p>Kevin Wong Ken Nam (MS2417121269)</p></li></ol>]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title>Observational Data Team A</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375076</link>
         <description><![CDATA[<p><a rel="noopener noreferrer nofollow" href="https://www.canva.com/design/DAGbDRiY4j0/SwumcD-CaSZKTHTr9GAD5g/edit?utm_content=DAGbDRiY4j0&amp;utm_campaign=designshare&amp;utm_medium=link2&amp;utm_source=sharebutton">https://www.canva.com/design/DAGbDRiY4j0/SwumcD-CaSZKTHTr9GAD5g/edit?utm_content=DAGbDRiY4j0&amp;utm_campaign=designshare&amp;utm_medium=link2&amp;utm_source=sharebutton</a></p>]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title>Observational Data Team B</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375077</link>
         <description><![CDATA[<p><a rel="noopener noreferrer nofollow" href="https://www.canva.com/design/DAGbDmCLbWE/vHRupge8FvwlOFsD1axBrA/edit?utm_content=DAGbDmCLbWE&amp;utm_campaign=designshare&amp;utm_medium=link2&amp;utm_source=sharebutton">https://www.canva.com/design/DAGbDmCLbWE/vHRupge8FvwlOFsD1axBrA/edit?utm_content=DAGbDmCLbWE&amp;utm_campaign=designshare&amp;utm_medium=link2&amp;utm_source=sharebutton</a></p>]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title>Youtube Experiment Video</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375078</link>
         <description><![CDATA[<p><a rel="noopener noreferrer nofollow" href="https://youtu.be/n8JW-8Yvi_E?feature=shared">https://youtu.be/n8JW-8Yvi_E?feature=shared</a></p>]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title>Compare and contrast the 3 classes of alcohol- include drawings, specific examples </title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375079</link>
         <description><![CDATA[]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title>(Individual) All 4 students must submit their discussion separately.  Write your name as the subject </title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375080</link>
         <description><![CDATA[]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title>Analyzing the Outcome</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375081</link>
         <description><![CDATA[<p><br></p><p><br></p>]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title>(Group) List ONE problem encountered for this experiment </title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375084</link>
         <description><![CDATA[]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title>(Group) Identify two precautions to improve the reliability of the experiment al results </title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375085</link>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title></title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375086</link>
         <description><![CDATA[]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title></title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375088</link>
         <description><![CDATA[]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title></title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375089</link>
         <description><![CDATA[]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375089</guid>
      </item>
      <item>
         <title>Izzaty</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375090</link>
         <description><![CDATA[<p>Explain the formation of two layers in the Lucas test.</p><p><br></p><ul><li><p><mark>When a secondary or tertiary alcohol reacts with the reagent, it forms a secondary or tertiary alkyl chloride. </mark></p></li><li><p><mark>The alkyl chloride is not soluble in the original layer.</mark></p></li><li><p><mark>The upper layer is clear and colourless which is water.  </mark></p></li><li><p><mark>The lower layer is alkyl chloride which insoluble in water.</mark></p></li><li><p><mark>Thus, the two layers are formed.</mark></p></li></ul><p><br></p><p><br></p><p>Suggest the chemical test to differentiate 1-propanol and 2-propanol. Include chemical equations and observations to support your suggestion. </p><p><br></p><p><strong>Chemical test : </strong><mark>Lucas Test</mark></p><p><strong>Observation :</strong></p><p>1-propanol : <mark>No cloudy solution formed even after 5 minutes heating.</mark></p><p><br></p><p>2-propanol : <mark>Cloudy solution formed within 10 minutes after heating.</mark></p>]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375090</guid>
      </item>
      <item>
         <title>Athirah</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375091</link>
         <description><![CDATA[<p>Explain the formation of two layers in the Lucas test.</p><p><br/></p><ul><li><p><mark>The formation of two layers in the Lucas Test is due to the formation of a secondary or tertiary alkyl chloride.</mark></p></li><li><p><mark>The upper layer is clear and colourless which is water.  </mark></p></li><li><p><mark>The lower layer is alkyl chloride which is insoluble in water.</mark></p></li><li><p><mark>Thus, the two layers are formed.</mark></p></li></ul><p><br/></p><p>Suggest the chemical test to differentiate 1-propanol and 2-methyl-2-propanol. Include chemical equations and observations to support your suggestion.</p><p><br/></p><p><strong><mark>Chemical test :</mark></strong><mark> Lucas Test</mark></p><p><br/></p><p><strong><mark>Observation :</mark></strong><mark> 1-propanol does not form cloudy solution even after heating while 2-methyl-2-propanol forms cloudy solution immediately</mark></p>]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375091</guid>
      </item>
      <item>
         <title>Kevin </title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375092</link>
         <description><![CDATA[<p>Explain the formation of two layers in the Lucas test.</p><p><br></p><ul><li><p>When a secondary or tertiary alcohol reacts with the reagent, it forms a secondary or tertiary alkyl chloride. </p></li><li><p>The alkyl chloride is not soluble in the original layer.</p></li><li><p>Water which is clear and colourless forms the upper layer.  </p></li><li><p>Alkyl chloride which insoluble in water forms the lower layer.</p></li><li><p>Thus, the two layers are formed.</p></li></ul><p><br></p><p><br></p><p><br></p><p>Suggest the chemical test to differentiate 1-pentanol and 2-methyl-2-propanol. Include chemical equations and observations to support your suggestion. </p><p><br></p><p>Chemical test: <mark>Lucas Test</mark></p><p>Observation: <mark>1-pentanol does not form cloudy solution within 10 minutes of heating.</mark></p><p>Observation: <mark>2-methyl-2-propanol forms cloudy solution immediately.</mark></p>]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375092</guid>
      </item>
      <item>
         <title>Leong</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375093</link>
         <description><![CDATA[<p>Explain the formation of two layers in the Lucas test.</p><ul><li><p><mark>When a secondary or tertiary alcohol reacts with the Lucas reagent, it forms a secondary or tertiary alkyl chloride and water. </mark></p></li><li><p><mark>The upper layer is clear and colourless which is water.  </mark></p></li><li><p><mark>The lower layer is alkyl chloride which insoluble in water.</mark></p></li><li><p><mark>Thus, the two layers are formed.</mark></p></li></ul><p><br/></p><p>Suggest the chemical test to differentiate 1-butanol and cyclobutanol. Include chemical equations and observations to support your suggestion. </p><p><strong>Chemical test : </strong><mark>Lucas Test</mark></p><p><strong>Observation:</strong> </p><ul><li><p><strong>1-butanol</strong> does not form cloudy solution even after heating for 10 minutes. (primary alcohol)</p></li><li><p><strong>cyclobutanol</strong> forms cloudy solution within 10 minutes after heating. (secondary alcohol)</p></li></ul><p><br/></p>]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      <item>
         <title></title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278375094</link>
         <description><![CDATA[]]></description>
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         <pubDate>2025-01-02 03:44:25 UTC</pubDate>
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      </item>
      <item>
         <title>Question 1</title>
         <author>m8130031</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278389857</link>
         <description><![CDATA[<p>Identify the class of alcohol for the above compound. </p><p><br></p><p>2-pentanol</p><p><br></p><p>Ans: Secondary</p>]]></description>
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         <pubDate>2025-01-02 04:09:12 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278389857</guid>
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         <title>Question 2</title>
         <author>m8130031</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278390268</link>
         <description><![CDATA[<p>What is the function of Lucas Test?</p><p><br></p><p>Ans:To identify the class of alcohol</p>]]></description>
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         <pubDate>2025-01-02 04:09:37 UTC</pubDate>
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      <item>
         <title>Question 3</title>
         <author>m8130031</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278390650</link>
         <description><![CDATA[<p>Which of the following alcohol does not turn cloudy when react with Lucas Reagent?</p><p><br></p><p>Ans: 2-methyl-2-butanol </p>]]></description>
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         <pubDate>2025-01-02 04:10:24 UTC</pubDate>
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         <title>Question 4</title>
         <author>m8130031</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278390759</link>
         <description><![CDATA[<p>What is the positive result for the reaction of alcohol with hot, acidified sodium dichromate?</p><p><br></p><p>Ans: Orange solution turns to green</p>]]></description>
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         <pubDate>2025-01-02 04:10:42 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278390759</guid>
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      <item>
         <title>Question 5</title>
         <author>m8130031</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278391065</link>
         <description><![CDATA[<p>Which of the following is not the precaution of the experiment? </p><p><br/></p><p>Ans: Arrange the chemical reagent in orderly.</p>]]></description>
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         <pubDate>2025-01-02 04:11:20 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278391065</guid>
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      <item>
         <title>CONCLUSION</title>
         <author>m8130031</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278391781</link>
         <description><![CDATA[<ol><li><p>Alcohol can be classified into <mark>primary alcohol</mark>, <mark>secondary alcohol</mark> and <mark>tertiary alcohol</mark>.</p></li><li><p><mark>Lucas</mark> test and <mark>oxidation</mark> reaction can be used to differentiate the three classes of alcohol.</p></li><li><p>Reaction with <mark>bromine water</mark> is used as confirmatory test for phenol.</p></li></ol>]]></description>
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         <pubDate>2025-01-02 04:13:07 UTC</pubDate>
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         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278644194</link>
         <description><![CDATA[<p>1-Butanol</p>]]></description>
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         <pubDate>2025-01-02 13:23:07 UTC</pubDate>
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      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278644330</link>
         <description><![CDATA[<p>2-Butanol</p>]]></description>
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         <pubDate>2025-01-02 13:23:17 UTC</pubDate>
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      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278644420</link>
         <description><![CDATA[<p>Alcohol X</p>]]></description>
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         <pubDate>2025-01-02 13:23:33 UTC</pubDate>
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      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278644515</link>
         <description><![CDATA[<p>Lucas reagent</p>]]></description>
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         <pubDate>2025-01-02 13:23:45 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278644515</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278644687</link>
         <description><![CDATA[<p>2-Methyl-2-propanol</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162947170/622e941da644a92cc0826714aeba3e25/1000012464.jpg" />
         <pubDate>2025-01-02 13:24:06 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278644687</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278644905</link>
         <description><![CDATA[<p>Concentrated H<sub>2</sub>SO<sub>4</sub></p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/ccc9ca7078a27b1d8d9f157e815e01da/IMG_7452_2.jpg" />
         <pubDate>2025-01-02 13:24:30 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278644905</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278645096</link>
         <description><![CDATA[<p>0.04M Na<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub></p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/1843887aee153ab223bd60854929f610/word_image5.png" />
         <pubDate>2025-01-02 13:24:57 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278645096</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278645221</link>
         <description><![CDATA[<p>Glacial acetic acid</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/a0a8b3cb4d178666717311644a847f07/glacial_acetic_acid_500x500_jpg.webp" />
         <pubDate>2025-01-02 13:25:11 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278645221</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278645290</link>
         <description><![CDATA[<p>Phenol</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/ad7f6c3bda103519fa6aa69cb9f5dbe0/IMG_7451.jpg" />
         <pubDate>2025-01-02 13:25:19 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278645290</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278645361</link>
         <description><![CDATA[<p>Bromine water</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/6d81ce068c8b56095ab5c2d51dcd0de0/IMG_7452.jpg" />
         <pubDate>2025-01-02 13:25:27 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278645361</guid>
      </item>
      <item>
         <title>(A) Lucas Test</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278646350</link>
         <description><![CDATA[<p>1. Approximately 1 mL of 1-butanol, 2-butanol, 2-methyl-2-propanol, and alcohol X were placed in 4 separate test tubes.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/4dce6198e6fa1c401b111be20ebd11fd/IMG_7087.JPG" />
         <pubDate>2025-01-02 13:27:24 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278646350</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278646898</link>
         <description><![CDATA[<p>2. 2 mL of Lucas reagent was added into the test tubes.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/77488998807ffa95452406c76e4be899/IMG_7457.jpg" />
         <pubDate>2025-01-02 13:28:09 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278646898</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278647547</link>
         <description><![CDATA[<p>3. A stopper was put, and the test tube was shaken.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/643f96d1681def5c03d9d372d4204fb9/IMG_7458.jpg" />
         <pubDate>2025-01-02 13:29:18 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278647547</guid>
      </item>
      <item>
         <title>(B) Oxidation</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278648896</link>
         <description><![CDATA[<p>1. 5 mL of 0.04M Na<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub> was placed in 4 separate test tubes.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162947170/71d28842b2f48b93f4c9367aab62d98f/1000012457.jpg" />
         <pubDate>2025-01-02 13:32:05 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278648896</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278649827</link>
         <description><![CDATA[<p>2. 2 or 3 drops of concentrated H<sub>2</sub>SO<sub>4</sub> was added to the Na<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub> solution in the fume cupboard.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162947170/9c1a4d1a379a6d016929fc0070cc596d/1000012458.jpg" />
         <pubDate>2025-01-02 13:33:12 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278649827</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278651605</link>
         <description><![CDATA[<p>3. 3 drops of 1-butanol, 2-butanol, 2-methyl-2propanol and alcohol X were added to each of the mixture accordingly.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162947170/ed4ce0ee17b679e818d92f1aa9023746/1000012459.jpg" />
         <pubDate>2025-01-02 13:36:35 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278651605</guid>
      </item>
      <item>
         <title>(C) Confirmatory Test For Phenol</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278652525</link>
         <description><![CDATA[<p>1. Approximately 1 mL of phenol solution was placed in a test tube.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/16656be5d59dbcd8eff0102a3c1fa22e/IMG_7451.jpg" />
         <pubDate>2025-01-02 13:38:01 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278652525</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278652911</link>
         <description><![CDATA[<p>2. Bromine water was added dropwise until precipitate was formed.</p><p> </p><p>3. The observation was recorded.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/d711f98a24bdbda06c7adcae039520db/IMG_7454.jpg" />
         <pubDate>2025-01-02 13:38:46 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3278652911</guid>
      </item>
      <item>
         <title>Athirah</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279159069</link>
         <description><![CDATA[<p><strong><mark>(A) Lucas Test</mark></strong></p><p><br></p><p><mark>Tertiary</mark> alcohol reacts the fastest with Lucas reagent as it is able to form a <mark>tertiary</mark> carbocation that is highly stable, <mark>primary</mark> alcohol does not give any result with Lucas reagent because <mark>primary</mark> carbocation is the least stable.</p><p><br></p><p>During the reaction of <mark>2-methyl-2-propanol</mark> with Lucas reagent, the formation of two layers immediately is due to the insolubility of <mark>2-methyl-2-chloropropane</mark> formed in the aqueous solution.</p><p><br></p><p>Alcohol X is a <mark>tertiary</mark> alcohol because <mark>Alcohol X forms cloudy solution immediately with two layers formed after reacting with Lucas reagent</mark>.</p><p><br></p><p><br></p><p><strong><mark>(B) Oxidation</mark></strong></p><p><br></p><p>1-butanol is a <mark>primary</mark> alcohol that is oxidised to <mark>1-butanoic acid</mark>. Orange colour of <mark>chromic acid</mark> turns green due to the reduction of <mark>Cr<sub>2</sub>O<sub>7</sub></mark> to <mark>Cr<sup>3+</sup></mark>.</p><p><br></p><p>2-butanol is a <mark>secondary</mark> alcohol that is oxidised to <mark>2-butanone</mark> and cannot be further oxidised.</p><p><br></p><p><br></p><p><strong><mark>(C) Confirmatory Test For Phenol</mark></strong></p><p><br></p><p>Phenol forms white precipitate, <mark>2,4,6-tribromophenol</mark> when reacted with bromine water.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162947170/0d3224620bfc4b767c02c6fab862ed68/1000012638.jpg" />
         <pubDate>2025-01-03 07:29:23 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279159069</guid>
      </item>
      <item>
         <title>Izzaty</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279159179</link>
         <description><![CDATA[<p><strong><mark>(A) Lucas Test</mark></strong></p><p><br></p><p><mark>Tertiary</mark> alcohol reacts the fastest with Lucas reagent as it is able to form a <mark>tertiary </mark>carbocation that is highly stable, primary alcohol does not give any result with Lucas reagent because primary carbocation is the least stable.</p><p><br></p><p>During the reaction of<mark> 2-methyl-2-propanol </mark>with Lucas reagent, the formation of two layers immediately is due to the insolubility of <mark>2-methyl-2-chloropropane</mark> formed in the aqueous solution.</p><p><br></p><p>Alcohol X is a <mark>tertiary</mark> alcohol because <mark>Alcohol X forms cloudy solution immediately with two layers formed after reacting with Lucas reagent</mark>.</p><p><br></p><p><strong>(B) Oxidation</strong></p><p><br></p><p>1-butanol is a <mark>primary</mark> alcohol that is oxidised to <mark>1-butanoic</mark> <mark>acid</mark>. Orange colour of chromic acid turns green due to the reduction of <mark>Cr<sub>2</sub>O<sub>7</sub></mark> to <mark>Cr<sup>3+</sup></mark>.</p><p><br></p><p>2-butanol is a <mark>secondary</mark> alcohol that is oxidised to 2-<mark>butanone</mark> and cannot be further oxidised.</p><p><br></p><p>2-methyl-2-propanol is a  alcohol that does not undergo oxidation because there is no <mark>hydrogen</mark> atom on the carbon atom attached to the OH group.</p><p><br></p><p><strong>(C) Confirmatory Test For Phenol</strong></p><p><br></p><p>Phenol forms white precipitate, <mark>2,4,6-tribromophenol</mark> when reacted with bromine water.</p><p><br></p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/2584113369/00fa2dc1863cb4957c2466bd5a6863fe/1000071860.png" />
         <pubDate>2025-01-03 07:29:41 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279159179</guid>
      </item>
      <item>
         <title>Leong</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279159200</link>
         <description><![CDATA[<p><strong><mark>(A) Lucas Test</mark></strong></p><p><br></p><p><mark>Tertiary</mark> alcohol reacts the fastest with Lucas reagent as it is able to form a <mark>tertiary</mark> carbocation that is highly stable, <mark>primary</mark> alcohol does not give any result with Lucas reagent because <mark>primary</mark> carbocation is the least stable.</p><p><br></p><p>During the reaction of <mark>2-methyl-2-propanol</mark> with Lucas reagent, the formation of two layers immediately is due to the insolubility of <mark>alkyl chloride</mark> formed in the aqueous solution.</p><p><br></p><p>Alcohol X is a <mark>tertiary</mark> alcohol because <mark>Alcohol X forms cloudy solution immediately with two layers formed after reacting with Lucas reagent</mark>.</p><p><br></p><p><br></p><p><strong><mark>(B) Oxidation</mark></strong></p><p><br></p><p>1-butanol is a <mark>primary</mark> alcohol that is oxidised to <mark>1-butanoic acid</mark>. Orange colour of <mark>chromic acid</mark> turns green due to the reduction of <mark>Cr<sub>2</sub>O<sub>7</sub></mark> to <mark>Cr<sup>3+</sup></mark>.</p><p><br></p><p>2-butanol is a <mark>secondary</mark> alcohol that is oxidised to <mark>2-butanone</mark> and cannot be further oxidised.</p><p><br></p><p><br></p><p><strong><mark>(C) Confirmatory Test For Phenol</mark></strong></p><p><br></p><p>Phenol forms white precipitate, <mark>2,4,6-tribromophenol</mark> when reacted with bromine water.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/8364aed04063511c4a639960a1b97692/IMG_7812.jpg" />
         <pubDate>2025-01-03 07:29:45 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279159200</guid>
      </item>
      <item>
         <title>Kevin</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279159225</link>
         <description><![CDATA[<p>(A) <strong><mark>Lucas</mark></strong> <strong><mark>Test</mark></strong></p><p><br></p><p><br></p><p>Tertiary alcohol reacts the fastest with Lucas reagent as it is able to form a <mark>tertiary</mark> carbocation that is highly stable, <mark>primary</mark> alcohol does not give any result with Lucas reagent because <mark>primary</mark> carbocation is the least stable.</p><p><br></p><p>During the reaction of <mark>2-methyl-2-propanol</mark> with Lucas reagent, the formation of two layers immediately is due to the insolubility of <mark>2-methyl-2-chloropropane</mark> formed in the aqueous solution.</p><p><br></p><p>Alcohol X is a <mark>tertiary</mark> alcohol because <mark>Alcohol X forms cloudy solution immediately with two layers formed after reacting with Lucas reagent</mark>.</p><p><br></p><p><br></p><p><br></p><p>(B) <mark>Oxidation</mark></p><p><br></p><p>1-butanol is a <mark>primary</mark> alcohol that is oxidised to <mark>1-butanoic</mark> acid. Orange colour of <mark>chromic acid</mark> turns green due to the reduction of <mark>Cr<sup>7+</sup></mark> to <mark>Cr<sup>3+</sup></mark>.</p><p><br></p><p><br></p><p><br></p><p>2-butanol is a <mark>secondary</mark> alcohol that is oxidised to <mark>2-butanone</mark> and cannot be further oxidised.</p><p><br></p><p><br></p><p><br></p><p>2-methyl-2-propanol is a  alcohol that does not undergo oxidation because there is no <mark>hydrogen</mark> atom on the carbon atom attached to the OH group.</p><p><br></p><p><br></p><p><br></p><p>(C) <mark>Confirmatory Test For Phenol</mark></p><p><br></p><p><br></p><p>Phenol forms white precipitate, <mark>2,4,6-tribromophenol</mark> when reacted with bromine water.</p><p><br></p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1280919823/db7a389a6792afa47484d5456ae308f0/1000070442.jpg" />
         <pubDate>2025-01-03 07:29:50 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279159225</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279163210</link>
         <description><![CDATA[<p>1. <a rel="noopener noreferrer nofollow" href="https://byjus.com/chemistry/lucas-test/">https://byjus.com/chemistry/lucas-test/</a></p>]]></description>
         <enclosure url="https://byjus.com/chemistry/lucas-test/" />
         <pubDate>2025-01-03 07:38:38 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279163210</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279163282</link>
         <description><![CDATA[<p>2. <a rel="noopener noreferrer nofollow" href="https://www.britannica.com/science/alcohol/Structure-and-classification-of-alcohols">https://www.britannica.com/science/alcohol/Structure-and-classification-of-alcohols</a></p>]]></description>
         <enclosure url="https://www.britannica.com/science/alcohol/Structure-and-classification-of-alcohols" />
         <pubDate>2025-01-03 07:38:48 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279163282</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279163382</link>
         <description><![CDATA[<p>3. <a rel="noopener noreferrer nofollow" href="https://byjus.com/chemistry/types-of-alcohols/">https://byjus.com/chemistry/types-of-alcohols/</a></p>]]></description>
         <enclosure url="https://byjus.com/chemistry/types-of-alcohols/" />
         <pubDate>2025-01-03 07:39:05 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279163382</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279163607</link>
         <description><![CDATA[<p>4. https://pubmed.ncbi.nlm.nih.gov/7171081/</p>]]></description>
         <enclosure url="https://pubmed.ncbi.nlm.nih.gov/7171081/" />
         <pubDate>2025-01-03 07:39:29 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279163607</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279163707</link>
         <description><![CDATA[<p>5. https://nutritionsource.hsph.harvard.edu/healthy-drinks/drinks-to-consume-in-moderation/alcohol-full-story/)</p>]]></description>
         <enclosure url="https://nutritionsource.hsph.harvard.edu/healthy-drinks/drinks-to-consume-in-moderation/alcohol-full-story/" />
         <pubDate>2025-01-03 07:39:40 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279163707</guid>
      </item>
      <item>
         <title>Problem encountered</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279165250</link>
         <description><![CDATA[<p>1. Long queue in front of the fume cupboard when handling the experiment. </p>]]></description>
         <enclosure url="" />
         <pubDate>2025-01-03 07:42:55 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279165250</guid>
      </item>
      <item>
         <title>Precaution steps</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279165440</link>
         <description><![CDATA[<p>1. Make sure to handle chemical reagents in a fume hood. </p><p><br/></p><p>2. Make sure to keep the chemical reagents closed because it is volatile.</p><p><br/></p><p>3. Make sure the temperature of water bath is within 70-80°C.</p>]]></description>
         <enclosure url="" />
         <pubDate>2025-01-03 07:43:24 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279165440</guid>
      </item>
      <item>
         <title>Similarities</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279166593</link>
         <description><![CDATA[<p>The 3 classes of alcohol have the same functional group, which is hyroxyl (-OH)</p>]]></description>
         <enclosure url="" />
         <pubDate>2025-01-03 07:46:38 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279166593</guid>
      </item>
      <item>
         <title>Differences</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279166813</link>
         <description><![CDATA[<p>The hydroxy carbon of primary alcohol is bonded to only one carbon , whereas secondary alcohol is bonded to two carbons, while tertiary alcohol is bonded to three carbon.</p>]]></description>
         <enclosure url="" />
         <pubDate>2025-01-03 07:47:13 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279166813</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279167267</link>
         <description><![CDATA[<p>The complexity of the alkyl chain of primary alcohol is unrelated to the classification of any alcohol considered as primary, whereas The two alkyl groups of secondary alcohol present may be either structurally identical or even different, while in tertiary alcohol, the presence of -OH group allows the alcohols in the formation of hydrogen bonds with their neighbouring atoms.</p>]]></description>
         <enclosure url="" />
         <pubDate>2025-01-03 07:48:18 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279167267</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279167648</link>
         <description><![CDATA[<p>The 3 classes of alcohol have the same general formula, which is C<sub>n</sub>H<sub>2n+1</sub>OH</p>]]></description>
         <enclosure url="" />
         <pubDate>2025-01-03 07:49:13 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3279167648</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287605206</link>
         <description><![CDATA[<p>3. The test tubes were heated in a water bath at 70°C - 80°C.</p><p><br/></p><p>4. The colour change was recorded.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162947170/b19e86a28e6f1723cd13818cb8186857/1000012466.jpg" />
         <pubDate>2025-01-12 06:47:10 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287605206</guid>
      </item>
      <item>
         <title></title>
         <author>bhmcnjq7w2</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655135</link>
         <description><![CDATA[<p>Stopper</p>]]></description>
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         <pubDate>2025-01-12 09:29:36 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655135</guid>
      </item>
      <item>
         <title></title>
         <author>bhmcnjq7w2</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655215</link>
         <description><![CDATA[<p>Dropper</p>]]></description>
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         <pubDate>2025-01-12 09:29:49 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655215</guid>
      </item>
      <item>
         <title></title>
         <author>bhmcnjq7w2</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655283</link>
         <description><![CDATA[<p>Test tube</p>]]></description>
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         <pubDate>2025-01-12 09:30:05 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655283</guid>
      </item>
      <item>
         <title></title>
         <author>bhmcnjq7w2</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655320</link>
         <description><![CDATA[<p>Stopwatch</p>]]></description>
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         <pubDate>2025-01-12 09:30:14 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655320</guid>
      </item>
      <item>
         <title></title>
         <author>bhmcnjq7w2</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655352</link>
         <description><![CDATA[<p>Water bath</p>]]></description>
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         <pubDate>2025-01-12 09:30:22 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655352</guid>
      </item>
      <item>
         <title></title>
         <author>bhmcnjq7w2</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655429</link>
         <description><![CDATA[<p>10 mL measuring cylinder</p>]]></description>
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         <pubDate>2025-01-12 09:30:36 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287655429</guid>
      </item>
      <item>
         <title></title>
         <author>bhmcnjq7w2</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287661867</link>
         <description><![CDATA[<p>4. The observation and the time taken for the reaction to occur was recorded.</p><p><br></p><p>5. The class of alcohol X was deduced.</p>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/508fb39971f8898c13ad9ea532d5f169/IMG_7122_2.jpg" />
         <pubDate>2025-01-12 09:45:09 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3287661867</guid>
      </item>
      <item>
         <title>Medicinal and health application</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3290093184</link>
         <description><![CDATA[<p>        Ethanol and isopropranol are found as an active ingredient in oral, parenteral, and topical prescription and nonprescription drug products.</p><p>        Although it is primarily used because of its solvent properties to help solubilize many drugs, it also possesses several concentration-dependent pharmacological actions, including sedative, carminative, cooling, antipyretic, rubefacient, cleansing, and antiseptic properties. Concentrations of 40% or more may be found in some oral preparations, thus resulting in patients consuming a significant amount of alcohol during the course of the day. A concise compilation of nearly 500 alcohol-containing prescription and nonprescription American drug products is presented.</p><p>        The table, which contains the proprietary drug name, manufacturer, type and concentration of alcohol, route of administration, and prescription : nonprescription status, is intended to aid clinicians in counseling patients receiving alcohol-deterrent drugs or patients in whom alcohol should be avoided.</p>]]></description>
         <enclosure url="" />
         <pubDate>2025-01-14 07:55:06 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3290093184</guid>
      </item>
      <item>
         <title>The pros of using alcohol in medicine</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3290103665</link>
         <description><![CDATA[<p>1. <strong>Better sensitivity :</strong> Alcohol has better sensitivity to insulin</p><p>2. <strong>Improve patient's health :</strong> Alcohol is able to improve the factors that influence blood clotting, such as tissue type plasminogen activator, fibrinogen, clotting factor VII, and von Willebrand factor</p>]]></description>
         <enclosure url="" />
         <pubDate>2025-01-14 08:04:44 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3290103665</guid>
      </item>
      <item>
         <title>The cons of using alcohol in medicine</title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3290104994</link>
         <description><![CDATA[<p>1. <strong>Toxicity</strong>: Alcohol can be toxic when consumed in prolonged periods, leading to liver damage, neurological impairments, and other health complications. </p><p>2. <strong>Addiction potential</strong>: Alcohol has addictive properties, and its use in medical treatments, if not carefully monitored, can contribute to substance abuse issues.</p><p><br></p>]]></description>
         <enclosure url="" />
         <pubDate>2025-01-14 08:06:09 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3290104994</guid>
      </item>
      <item>
         <title></title>
         <author>athirahak</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3290112635</link>
         <description><![CDATA[<p>6. https://www.google.com/url?sa=t&amp;source=web&amp;rct=j&amp;opi=89978449&amp;url=https://penndentalmedicine.org/blog/is-alcohol-bad-for-your-teeth/#:~:text=But the negative links between,greater risk of oral cancer.&amp;ved=2ahUKEwjRnLO04fSKAxVMfGwGHSWYDmEQFnoECCEQBQ&amp;usg=AOvVaw0xm-XGHXpPToPSZYv7y-_G</p>]]></description>
         <enclosure url="https://www.google.com/url?sa=t&amp;source=web&amp;rct=j&amp;opi=89978449&amp;url=https://penndentalmedicine.org/blog/is-alcohol-bad-for-your-teeth/#:~:text=But the negative links between,greater risk of oral cancer.&amp;ved=2ahUKEwjRnLO04fSKAxVMfGwGHSWYDmEQFnoECCEQBQ&amp;usg=AOvVaw0xm-XGHXpPToPSZYv7y-_G" />
         <pubDate>2025-01-14 08:13:21 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3290112635</guid>
      </item>
      <item>
         <title>(B) Oxidation with sodium dichromate</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3291878868</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/2584113369/00fda22bafe8823f5e16be69071f7aaf/1000071740.jpg" />
         <pubDate>2025-01-15 11:18:39 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3291878868</guid>
      </item>
      <item>
         <title>(C) Confirmatory test for phenol</title>
         <author>izzyn0611</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3291879867</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/2584113369/34d0fd8d21de85236d659cee527dccf3/1000071741.jpg" />
         <pubDate>2025-01-15 11:19:17 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3291879867</guid>
      </item>
      <item>
         <title>Mindmap</title>
         <author>bhmcnjq7w2</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3292313767</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/8268c6021ceb67232265866082bdd153/Purple_Colorful_Organic_Mind_Map_Brainstorm.png" />
         <pubDate>2025-01-15 16:44:40 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3292313767</guid>
      </item>
      <item>
         <title>A) Lucas Test</title>
         <author>m8130031</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3292928907</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1280919823/ef23813ea3dc7dccf40d65083dff11d1/1000070429.jpg" />
         <pubDate>2025-01-16 03:21:20 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3292928907</guid>
      </item>
      <item>
         <title>Table compare and contrast 3 classes of alcohol </title>
         <author>bhmcnjq7w2</author>
         <link>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3292965613</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/3162919869/dd177ed973a373874163ebcdd38b6e2f/IMG_7810.jpg" />
         <pubDate>2025-01-16 04:07:45 UTC</pubDate>
         <guid>https://padlet.com/izzyn0611/n6bnlvvxon5jv3k1/wish/3292965613</guid>
      </item>
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