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      <title>PHENOL by Bhuvana Chezian</title>
      <link>https://padlet.com/hodchehscpm/phenols</link>
      <description>Post any two reactions related to phenol (preparation or reactions of phenol) . Mention the reactant, Product and reagents used.</description>
      <language>en-us</language>
      <pubDate>2021-08-27 05:53:02 UTC</pubDate>
      <lastBuildDate>2025-12-15 17:34:59 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>&lt;Reactions of Phenol&gt;</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1700358394</link>
         <description><![CDATA[<div>1. Phenol on hydrogenation using <strong>Nickel catalyst at 160 deg celsius</strong>, gets reduced into <strong><em>Cyclohexanol</em></strong>&nbsp; <em>[Reduction]</em><br>2. Phenol on treatment with <strong>nitrous acid at 278 K</strong> produces <strong><em>Para-nitroso phenol</em></strong>&nbsp; <em>[Nitrosation]<br><br></em><br></div><blockquote><pre><em>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; </em><em><sub>&nbsp;Rahul Balaji M.S. 12 C</sub></em></pre></blockquote>]]></description>
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         <pubDate>2021-08-27 06:55:35 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1700358394</guid>
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         <title></title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1700386838</link>
         <description><![CDATA[<div><strong>Reactions of Phenol.<br>&nbsp; &nbsp; &nbsp; 1.Reaction with Zn dust</strong></div><ul><li><strong>phenol is converted to</strong><strong><mark> benzene</mark></strong><strong> on heating with Zn dust. During the reaction the</strong><strong><mark> hydroxyl group</mark></strong><strong> attached to aromatic ring gets eliminated.</strong></li></ul><div>&nbsp; &nbsp; &nbsp; <strong>2.Reaction with Ammonia.&nbsp;</strong></div><ul><li><strong>Phenol on heating with ammonia in presence of </strong><strong><mark>anhydrous ZnCl2</mark></strong><strong> gives</strong><strong><mark> aniline.</mark></strong></li></ul><div>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; vishal.m XII-A</div><div><br><br></div>]]></description>
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         <pubDate>2021-08-27 07:18:04 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1700386838</guid>
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      <item>
         <title>PREPARATION OF PHENOL</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1700542641</link>
         <description><![CDATA[<div>1. From halo arenes (Dows process)<br>When Chlorobenzene is hydrolysed with <strong><mark>6-8% NaOH at 300 bar and 633K</mark></strong> in a closed vessel <strong><mark>sodium phenoxide </mark></strong>is formed which on treatment with <strong><mark>dilute HCI</mark></strong> gives <strong><mark>phenol</mark></strong>.<br>2. From benzene sulphonic acid<br>Benzene is sulphonated with <strong><mark>oleum</mark></strong> and the <strong><mark>benzene sulphonic acid</mark></strong> so formed is heated with <mark>molten NaOH at 623K</mark> gives <mark>sodium phenoxide</mark> which on acidification gives<strong><mark> phenol</mark></strong>.<br><br>&nbsp; &nbsp;KAVIYA.V XII-B</div>]]></description>
         <enclosure url="https://www.eptes.com/wp-content/uploads/2018/08/Phenol.jpg" />
         <pubDate>2021-08-27 09:29:28 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1700542641</guid>
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      <item>
         <title>Give two reactions that show the acidic nature of phenol.</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1700724010</link>
         <description><![CDATA[<div>Two reactions that show the acidic nature of phenol are as follows:<br>(i) The reaction of phenol with sodium to form sodium phenoxide with liberation of hydrogen gas.<br>C6​H5​OH+Na→C6​H5​−ONa+1/2H2​↑<br>(ii) The reaction of phenol with sodium hydroxide to give sodium phenoxide and water.<br>C6​H5​−OH+NaOH→C6​H5​−ONa+H2​O<br>Phenol is more acidic than ethanol.<br>Deprotonation of phenol gives phenoxide ion which is resonance stabilized.<br>There is no resonance stabilization for the deprotonation of ethoxide ion (obtained by deprotonation of ethanol).<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;JAGADEEP<br>                                                           XII-B</div>]]></description>
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         <pubDate>2021-08-27 12:58:09 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1700724010</guid>
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         <title>Reaction of phenol:</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1701656446</link>
         <description><![CDATA[<div>i)The reaction of phenol with sodium to form sodium phenoxide with liberation of hydrogen gas.<br>C6​H5​OH+Na→C6​H5​−ONa+1/2H2↑<br>(ii) The reaction of phenol with sodium hydroxide to give sodium phenoxide and water.<br>C6​H5​−OH+NaOH→C6​H5​−ONa+H2​O<br>Phenol is more acidic than ethanol.<br>Deprotonation of phenol gives phenoxide ion which is resonance stabilized.<br>There is no resonance stabilization for the deprotonation of ethoxide ion (obtained by deprotonation of ethanol).&nbsp;<br>R.Harini 12c</div>]]></description>
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         <pubDate>2021-08-28 02:38:55 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1701656446</guid>
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      <item>
         <title>REACTION OF PHENOL</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1701715436</link>
         <description><![CDATA[<div>(1) The reaction of phenol with sodium to form sodium phenoxide with liberation of hydrogen gas.<br>&nbsp;C6​H5​OH+Na--&gt;C6​H5​−ONa+1/2H2↑<br>(2) phenol is reacted with zn dust to form benzene on heating<br> C6H5OH+ZN--on heating--&gt;C6H6+ZNO<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; -NITHEEESHWARI.S 12A</div>]]></description>
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         <pubDate>2021-08-28 04:19:41 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1701715436</guid>
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         <title>Reactions of Phenol</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1701821927</link>
         <description><![CDATA[<div><strong>i)PHTHALEIN RXN : </strong><em>Reactant</em>-phenol, ophthalic anhydride, <em>Conditions</em>- on heating in the presence of con.H2SO4 , <em>Product</em>- phenolphthalein.<br><strong>ii)COUPLING RXN </strong>: <em>Reactant</em>- Benzene diazonium chloride, phenol, <em>Conditions</em>- temp at 273-278K in the presence of NaOH, <em>Product</em>- p-hydroxy azobenzene.</div><blockquote>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; - E.Navitha, XII-B</blockquote>]]></description>
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         <pubDate>2021-08-28 08:21:48 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1701821927</guid>
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      <item>
         <title>Reactions of Phenols </title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1701870312</link>
         <description><![CDATA[<div>Kolbe's Reaction<br>In this reaction the phenol is treated with Sodium Hydroxide which forms Sodium phenoxide by removal of H2O<br>Then this Sodium phenoxide is treated with CO2 under 4 to 7 bar pressure in 400k which forms Sodium salicylate which on acid hydrolysis gives salicylic acid.<br><br><br><strong>Phthalein Reaction</strong><br>Phallic Anhydride which is treated with concentrated H2SO4 forms phenolpthalein&nbsp;<br>                                    J Nithyashree 12c</div>]]></description>
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         <pubDate>2021-08-28 10:19:20 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1701870312</guid>
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         <title>PREPARATION OF PHENOL FROM CUMENE:                                  Cumene in the presence of air gives cumene hydro-peroxide.The reaction between cumene hydroxide and dilute acid gives phenol and acetone (as a byproduct).</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1702344051</link>
         <description><![CDATA[<div>&nbsp;                   </div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1286330612/c84b52dc01ca2d883c3c9b6f0ee0ce12/image.png" />
         <pubDate>2021-08-29 04:30:27 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1702344051</guid>
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         <title>Reactions of alcohol </title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1702426856</link>
         <description><![CDATA[<div>1. Phenol is converted into benezene on heating with zinc dust&nbsp;<br>C6+H5 +Zn -&nbsp; C6H5+ZnO<br>2. Phenol reacts with dilute nitric acid&nbsp; at a room temperatures to give a mixture of 2-nitrophenol and 4-nitrophenol while with the concentrated nitric acid .<br>3. Aqueous solutions of phenol are weakly acidic and turns blue litmus slightly to red.<br>S. Umesh Kumar&nbsp;<br>XII-A </div>]]></description>
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         <pubDate>2021-08-29 06:56:24 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1702426856</guid>
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         <title>REACTIONS OF PHENOL:</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1702522082</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1065206681/d98442d830e824373d91c1ef688ffe9a/20210829_145121380.jpg" />
         <pubDate>2021-08-29 09:24:22 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1702522082</guid>
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         <title>REACTION OF PHENOL:</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1702527761</link>
         <description><![CDATA[<div>1. The aqueous mixture of phenol is weakly acidic and changes blue litmus somewhat to red. <br>C6H5OH + NaOH → C6H5ONa + H2O<br><br><strong>2.Schotten-Baumann reaction:<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; When a mixture of phenol and benzoyl chloride is shaken in the occurrence of dilute sodium hydroxide solution, phenyl benzoate is produced.&nbsp;<br>C6H5OH + C6H5COCl → C6H5OCOC6H5 + HCl<br><br>3. Phenol is transformed to benzene when it is distilled with zinc dust.<br>C6H5OH + Zn → C6H6 + ZnO<br><br>&nbsp; &nbsp;- R . JENISHA 12C<br></strong><br></div>]]></description>
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         <pubDate>2021-08-29 09:33:46 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1702527761</guid>
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         <title>Reactions of Phenol</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1702684703</link>
         <description><![CDATA[<div>1)Phenol + zn Dust when heating gives Benzene&nbsp;<br>C6 H5 OH + Zn gives C6 H6 + ZnO<br>2) Coupling Reaction:<br>In this Reaction the Benzene Diazonium Chloride combines with Phenol with the presence of Naoh at the temperature 273-278k gives Hydrozxy Azo Benzene. &nbsp;<br>&nbsp; &nbsp; &nbsp; &nbsp;- Deepika S    12 A </div>]]></description>
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         <pubDate>2021-08-29 14:08:45 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1702684703</guid>
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         <title>Reaction of phenol</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1702686034</link>
         <description><![CDATA[<ul><li><strong><em>Coupling Rxn:&nbsp;</em></strong></li></ul><div>Benzene diazonium chloride reacts with phenol at temperature 273-278 K&nbsp; with NAOH it forms&nbsp; P-hydroxy azobenzene .</div><ul><li><em>Rxn with Zn dust:</em></li></ul><div>Phenol reacts with Zn at high temperature to form Benzene.&nbsp;<br>                         -S.Priyadharshini of 12C   </div><div><br></div>]]></description>
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         <pubDate>2021-08-29 14:10:30 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1702686034</guid>
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         <title>Reaction of phenol</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1702758038</link>
         <description><![CDATA[<div>1.Nitration:<br>Phenol on treatment with nitrous acid at 278 K produces Para-nitroso phenol<br><br>2.WITH ZN DUST:<br>phenol is converted to benzene on heating with Zn dust. During the reaction the hydroxyl group attached to aromatic ring gets eliminated.<br><br> S.Anirudh 12 B<br><br></div>]]></description>
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         <pubDate>2021-08-29 15:57:03 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1702758038</guid>
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         <title>The reaction of phenol</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1702853770</link>
         <description><![CDATA[<div>i)the reaction of phenol with sodium to form sodium phenoxide with the liberation of hydrogen gas.C6​H5​OH+Na→C6​H5​−ONa+1/2H2↑<br>(ii) The reaction of phenol with sodium hydroxide to give sodium phenoxide and water.C6​H5​−OH+NaOH→C6​H5​−ONa+H2​O Phenol is more acidic than ethanol. Deprotonation of phenol gives phenoxide ion which is resonance stabilized. There is no resonance stabilization for the deprotonation of ethoxide ion.<br>M.Hrithik Roshan<br>12-B</div>]]></description>
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         <pubDate>2021-08-29 18:46:11 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1702853770</guid>
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         <title></title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1703425406</link>
         <description><![CDATA[<div>Phenol reacts with dilute nitric acid at room temperature to give a mixture of <strong>2-nitrophenol and 4-nitrophenol</strong> while with concentrated nitric acid, additional nitro groups are introduced, e.g. to give 2,4,6-trinitrophenol.<br>          Sahithya. R</div>]]></description>
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         <pubDate>2021-08-30 02:39:12 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1703425406</guid>
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         <title>Reactions of phenol</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1703456336</link>
         <description><![CDATA[<div><strong>Nitrosation<br></strong>Phenol reacts with conc. HNO3 in the presence of conc. H2SO4 gives trinitro-phenol. <br><strong>Coupling RXN<br></strong>Benzene diazonium chloride reacts with phenol in the presence of NaOH at temperature between 273-278K to produce p- hydroxyazobenzene<br><strong>Phthalein RXN<br></strong>Phenol with phallic anhydride heated in presence of conc. H2SO4 gives phenophthalene and H2O<br>-S. Pragalya, 12B</div>]]></description>
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         <pubDate>2021-08-30 02:50:03 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1703456336</guid>
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         <title>Reactions of phenol:</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1703599292</link>
         <description><![CDATA[<div><strong><em>1)Nitration:<br>&nbsp; &nbsp; &nbsp; &nbsp; Nitration with conc.HNO3+Conc.H2SO4 gives picric acid at 298K.<br><br>2)Sulphonation:<br>&nbsp; &nbsp; &nbsp; &nbsp;Phenol reacts with conc.H2SO4 at 280K<br>to form o-phenol sulphonic acid as the major product</em></strong>.<br>                                                           -Pavithra.R 12 A </div>]]></description>
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         <pubDate>2021-08-30 03:47:44 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1703599292</guid>
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         <title> </title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1703865179</link>
         <description><![CDATA[<div>Phenol reacts with dilute nitric acid at room temperature to give a mixture of 2-nitrophenol and 4 nitrophenol while with concentrated nitric acid, additional nitro groups are introduced, e.g. to give 2,4,6 trinitrophenol.<br><br>Reaction of phenol<br>Sodium Hydroxide. Because phenol is acidic, it reacts with sodium hydroxide to form the phenoxide anion and water.<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Kanishka v<br>                                                12 A</div>]]></description>
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         <pubDate>2021-08-30 05:57:07 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1703865179</guid>
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         <title>REACTIONS OF PHENOL:</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1703907559</link>
         <description><![CDATA[<ul><li><strong><em><mark>1. Sulphonation:</mark></em></strong></li></ul><div>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;<strong><em>&nbsp; Phenol reacts with conc.H2SO4 at 280K to form o-phenol sulphonic acid. When the reaction is carried out at 373K, the major product is p-phenol sulphonic acid.<br><br></em></strong><br></div><ul><li><strong><em><mark>2. Nitrosation:</mark></em></strong></li></ul><div><strong><em>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Phenol reacts with HNO2 at 278K to give p-nitroso phenol.<br><br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;- S.SUBRAMANIAN &nbsp; XII-A</em></strong></div>]]></description>
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         <pubDate>2021-08-30 06:20:13 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1703907559</guid>
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      <item>
         <title>REACTION OF PHENOL</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1704181394</link>
         <description><![CDATA[<div>Halogenation:<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Phenol reacts with bromine water to give a white precipitate of 2,4,6-tri bromo phenol.If the reaction is carried out in cs2 or ccl4 at 278K, a mixture of ortho and para bromo phenols are formed.<br><br>KOLBE'S REACTION:<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;In this reaction, phenol is first converted into sodium peroxide which is more reactive than phenol towards electrophilic substitution reaction with co2. Treatment of sodium phenoxide with co2 at 400K, 4-7 bar pressure followed by acid hydrolysis gives salicylic acid.<br><br><em>A.VARUN <br>XII-A </em><br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;</div>]]></description>
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         <pubDate>2021-08-30 09:22:12 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1704181394</guid>
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         <title>Reactions of phenol</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1704428422</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-08-30 12:59:43 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1704428422</guid>
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         <title>Reaction of phenol:</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1704566489</link>
         <description><![CDATA[<div># <mark>Nitration</mark>: <br> Phenol on treatment with nitrous acid at 278k produces Para nitro phenol<br># <mark>with zn dust&nbsp;</mark>:&nbsp;<br>Phenol is convert to benzene on heating with zn dust during the reaction the hydroxyl group attached to aromatic rings gets elimated<br>   - P.ASHWINI PRIYA 12 B</div>]]></description>
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         <pubDate>2021-08-30 14:03:34 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1704566489</guid>
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         <title>REACTIONS OF PHENOL </title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1704688260</link>
         <description><![CDATA[<blockquote>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; -<em><mark>GOKUL G, XII-A</mark></em></blockquote><div><br></div>]]></description>
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         <pubDate>2021-08-30 14:52:08 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1704688260</guid>
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         <title>REACTIONS OF PHENOL</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1704709118</link>
         <description><![CDATA[<div>MONISHA S<br>12 C</div>]]></description>
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         <pubDate>2021-08-30 15:01:40 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1704709118</guid>
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         <title> reaction of phenol </title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1704747545</link>
         <description><![CDATA[<div>Swetharini .L XIIC C</div>]]></description>
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         <pubDate>2021-08-30 15:17:06 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1704747545</guid>
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         <title></title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1704831646</link>
         <description><![CDATA[<div>PREPARATION OF PHENOL 🧪<br><em>Aniline is </em><em><mark>diazotized</mark></em><em> with </em><em><mark>nitrous acid</mark></em><em>&nbsp; at 273-278K to give </em><em><mark>benzene</mark></em><em>&nbsp;</em></div><blockquote><em><mark>diazonium chloride</mark></em><em> which on further treatment with </em><em><mark>hot water</mark></em><em> in the presence of mineral acid&nbsp;</em></blockquote><div><em>gives </em><em><mark>phenol</mark></em><em>.<br>REACTION OF PHENOL</em></div><ul><li><em>Phenol is converted to benzene on </em><em><mark>heating</mark></em><em> with zinc dust. In this reaction the </em><em><mark>hydroxyl group</mark></em><em> which is attached to the aromatic ring is </em><em><mark>eliminated</mark></em><em>.</em></li></ul>]]></description>
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         <pubDate>2021-08-30 15:53:10 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1704831646</guid>
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         <title>REACTIONS OF PHENOL:</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1704854581</link>
         <description><![CDATA[<div><br>1. Sulphonation:<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Phenol reacts with conc.H2SO4 at 280K to form ortho-phenol sulphonic acid. When the reaction is carried out at 373K, the major product is para-phenol sulphonic acid.<br>2. Nitrosation:<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Phenol reacts with HNO2 at 278K to give para-nitroso phenol.<br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; -Sneka. M;12-B</div>]]></description>
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         <pubDate>2021-08-30 16:04:07 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1704854581</guid>
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         <title>REACTIONS OF PHENOL:</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1704998290</link>
         <description><![CDATA[<div><strong><em><mark>1. Nitrosation:-</mark></em></strong></div><div><strong><em>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Phenol </em></strong>reacts with HNO2 at 278K to give<strong><em> p-nitrosophenol.</em></strong></div><div><br><strong><em><mark>2. Reduction:-</mark></em></strong></div><div><strong><em>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Phenol </em></strong>on hydrogenation using Ni catalyst at 160°C, gets reduced into<strong> </strong><strong><em>Cyclohexanol<br><br>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;           &nbsp; &nbsp; &nbsp; Navishraja .S XII C</em></strong></div>]]></description>
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         <pubDate>2021-08-30 17:15:35 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1704998290</guid>
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         <title>Reaction of phenol</title>
         <author></author>
         <link>https://padlet.com/hodchehscpm/phenols/wish/1718909819</link>
         <description><![CDATA[<div>&nbsp; &nbsp; &nbsp; &nbsp; Phenol reacts with dilute nitric acid at room temperature to give a mixture of 2-nitrophenol and 4-nitrophenol while with concentrated nitric acid, additional nitro groups are introduced, e. g. to give 2,4,6-trinitrophenol. Aqueous solutions of phenol are weakly acidic and turn blue litmus slightly to red.&nbsp; &nbsp;&nbsp;<br>                       -Hemamalar D, 12 "C"</div>]]></description>
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         <pubDate>2021-09-06 08:28:13 UTC</pubDate>
         <guid>https://padlet.com/hodchehscpm/phenols/wish/1718909819</guid>
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