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      <title>Aminas y derivados by Santiago Gonzalez</title>
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      <description>Hecho con ♥</description>
      <language>en-us</language>
      <pubDate>2020-11-22 16:13:38 UTC</pubDate>
      <lastBuildDate>2024-12-13 09:31:01 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>Definición de aminas</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/950029872</link>
         <description><![CDATA[<ul><li>Las aminas son derivados orgánicos del amoniaco y resultan de la sustitución de los hidrógenos de la molécula por los radicales alquilo, según se sustituyan uno, dos o tres hidrógenos, las aminas serán primarias, secundarias o terciarias. Las aminas contienen un átomo de nitrógeno con un par de electrones no enlazado, lo que hace a las aminas básicas y nucleofilicas. <strong>McMurry, J., (2012).</strong></li></ul>]]></description>
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         <pubDate>2020-11-22 17:08:42 UTC</pubDate>
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      <item>
         <title>Obtención de las aminas</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/950276014</link>
         <description><![CDATA[<div>Los nitrilos se pueden preparar por reacción de halo alcanos con cianuro de sodio; posteriormente los nitrilos se reducen con LiAlH4 produciendo aminas. <strong>Tareasplus. (2013).</strong></div>]]></description>
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         <pubDate>2020-11-22 19:43:32 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/950276014</guid>
      </item>
      <item>
         <title>Mecanismo de reacción </title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/950382581</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-22 20:57:26 UTC</pubDate>
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      </item>
      <item>
         <title>Síntesis de la acetanilida</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/950713062</link>
         <description><![CDATA[<div>Una amina puede ser tratada con anhídrido de acido para formar una amida.  la anilina que es la amina aromática primaria mas sencilla reacciona con anhídrido acético para formar acetanilida y acido acético. <strong>Villanueva, H. (2012). </strong></div>]]></description>
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         <pubDate>2020-11-23 01:29:52 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/950713062</guid>
      </item>
      <item>
         <title>Mecanismo de reacción</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/953995302</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-23 20:44:30 UTC</pubDate>
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      <item>
         <title>Parte Procedimental</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/953999275</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-23 20:46:01 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/953999275</guid>
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      <item>
         <title>2 Parte procedimental</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954098347</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-23 21:25:54 UTC</pubDate>
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      <item>
         <title>3 Parte procedimental</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954166407</link>
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         <pubDate>2020-11-23 21:59:21 UTC</pubDate>
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      <item>
         <title></title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954181623</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-23 22:07:25 UTC</pubDate>
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      </item>
      <item>
         <title>Producto solido cristalizado</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954182824</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-23 22:08:04 UTC</pubDate>
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      </item>
      <item>
         <title>Síntesis de la benzamida</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954643649</link>
         <description><![CDATA[<div>El método de schotten-baumann es un método muy sencillo de acilación en el cual una amina se puede convertir cuatitativamente en una amida. <strong>Allinger, L. (1984). </strong></div>]]></description>
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         <pubDate>2020-11-24 02:23:01 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954643649</guid>
      </item>
      <item>
         <title>Mecanismo de reacción</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954869320</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-24 04:46:21 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954869320</guid>
      </item>
      <item>
         <title>Parte procedimental</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954876796</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-24 04:50:36 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954876796</guid>
      </item>
      <item>
         <title>Producto solido</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954897960</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-24 05:03:43 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/954897960</guid>
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      <item>
         <title>Formación de picratos</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/956865845</link>
         <description><![CDATA[<div>Los picratos son formados por la reacción del acido pícrico con metales, sales metálicas , bases y amoniaco. <strong>De Química. (2020). <br></strong><br></div>]]></description>
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         <pubDate>2020-11-24 16:23:40 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/956865845</guid>
      </item>
      <item>
         <title>Mecanismo de reacción</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957116181</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-24 17:23:28 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957116181</guid>
      </item>
      <item>
         <title>Parte procedimental</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957191597</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-24 17:42:20 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957191597</guid>
      </item>
      <item>
         <title>Formación de aminas</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957621820</link>
         <description><![CDATA[<div>La prueba de Hinsberg es una reacción Química que se usa para distinguir entre aminas primarias, secundarias y terciarias. T<strong>ube, O. (2020,)</strong></div>]]></description>
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         <pubDate>2020-11-24 19:32:29 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957621820</guid>
      </item>
      <item>
         <title></title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957675437</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-24 19:48:07 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957675437</guid>
      </item>
      <item>
         <title></title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957682083</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-24 19:50:03 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957682083</guid>
      </item>
      <item>
         <title>Mecanismo de reacción</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957682623</link>
         <description><![CDATA[<div>Amina primaria.</div>]]></description>
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         <pubDate>2020-11-24 19:50:13 UTC</pubDate>
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      </item>
      <item>
         <title>Amina secundaria</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957704850</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-24 19:57:21 UTC</pubDate>
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      </item>
      <item>
         <title>Amina Terciaria</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957719872</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-24 20:02:11 UTC</pubDate>
         <guid>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957719872</guid>
      </item>
      <item>
         <title>Parte procedimental</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957727169</link>
         <description><![CDATA[]]></description>
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         <pubDate>2020-11-24 20:04:33 UTC</pubDate>
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      <item>
         <title>Producto solido</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/957829552</link>
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         <pubDate>2020-11-24 20:41:16 UTC</pubDate>
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      <item>
         <title>2 parte procedimental</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/958027526</link>
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         <pubDate>2020-11-24 22:14:33 UTC</pubDate>
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      </item>
      <item>
         <title>Formación del yoduro de amonio</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/958098725</link>
         <description><![CDATA[<div>El amoníaco y las aminas reaccionan con yodometano para formar yoduros de amonio. En estos iones de amonio cuaternario que se pueden producir, la amina se libera usando una base.  Ege, S. (2000).<br><br></div>]]></description>
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         <pubDate>2020-11-24 22:57:54 UTC</pubDate>
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      <item>
         <title></title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/960658585</link>
         <description><![CDATA[<div><strong>Tareasplus. (2013, 04, 26). Síntesis de aminas por reducción de nitrilo. [Archivo del video]. Recuperado el 2020, 11, 22 en: https://www.youtube.com/watch?v=skf9WuLZo0c.<br><br>Villanueva, H. (2012). </strong><strong><em>Experimento 6 Síntesis de acetanilida.</em></strong><strong> Recuperado el 2020, 11, 23 en: https://es.slideshare.net/mtapizque/sintesis-de-acetanilida#:~:text=En%20este%20experimento%2C%20anilina%2C%20la,la%20amida%2C%20y%20%C3%A1cido%20ac%C3%A9tico.&amp;text=Principalmente%2C%20reacciona%20vigorosamente%20liberando%20HCl,de%20participar%20en%20la%20reacci%C3%B3n.<br><br>Allinger, L. (1984). </strong><strong><em>Química Orgánica. </em></strong><strong>Barcelona. Editoral Reverte S.A.<br><br>De Química. (2020). </strong><strong><em>Aminas</em></strong><strong>. Recuperado el 2020, 11, 24 en: https://www.dequimica.info/aminas/<br><br>Tube, O. (2020, 07, 11). </strong></div><h1><strong><em>Mecanismo de la Reacción de Hinsberg-Identificación de Aminas-Marcha de Laboratorio. </em></strong><strong>[Archivo de video].  Recuperado el 24, 11, 24 en:  https://www.youtube.com/watch?v=M8_scX2LAUE.</strong></h1><div><strong><br>Ege, S. (2000). Química Orgánica Estructura y reactividad. Barcelona. Editorial Reverte S.A. <br><br><br><br><br><br><br><br></strong><br></div>]]></description>
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         <pubDate>2020-11-25 17:20:10 UTC</pubDate>
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      <item>
         <title>Parte procedimental</title>
         <author>santigonzalez2299</author>
         <link>https://padlet.com/santigonzalez2299/zxd5jm5jk4sqf8kl/wish/961247166</link>
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         <pubDate>2020-11-25 19:39:18 UTC</pubDate>
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         <title>Producto solido cristalino</title>
         <author>santigonzalez2299</author>
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         <pubDate>2020-11-25 20:52:15 UTC</pubDate>
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      <item>
         <title>Producto cristalino solido</title>
         <author>santigonzalez2299</author>
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         <pubDate>2020-11-27 15:43:48 UTC</pubDate>
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