<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0187-893X</journal-id>
<journal-title><![CDATA[Educación química]]></journal-title>
<abbrev-journal-title><![CDATA[Educ. quím]]></abbrev-journal-title>
<issn>0187-893X</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional Autónoma de México, Facultad de Química]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0187-893X2022000300061</article-id>
<article-id pub-id-type="doi">10.22201/fq.18708404e.2022.3.81302</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[H-Bridges with OH Donors in Organic Chemistry]]></article-title>
<article-title xml:lang="es"><![CDATA[Donadores de Puentes de Hidrógeno con Grupos OH en Química Orgánica]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lamoureux]]></surname>
<given-names><![CDATA[Guy]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Chaves-Carballo]]></surname>
<given-names><![CDATA[Katherine]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de Costa Rica Escuela de Química y Centro de Investigaciones en Productos Naturales (CIPRONA) ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Costa Rica</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad de Costa Rica Escuela de Química y Centro de Investigaciones en Productos Naturales (CIPRONA) ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Costa Rica</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2022</year>
</pub-date>
<volume>33</volume>
<numero>3</numero>
<fpage>61</fpage>
<lpage>79</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0187-893X2022000300061&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0187-893X2022000300061&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0187-893X2022000300061&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract This article discusses the H-bridge formation amongst functional groups containing different H-bridge acceptors with OH donors. A series of circular grids is introduced as a visual aid for the organization and the comparison of the diversity of H-bridges present in organic molecules, emphasizing in the case where the H-bridge donor is an OH group (primarily alcohols and phenols). The H-bridges are classified as &#8220;unlikely&#8221;, &#8220;less significant&#8221; and &#8220;significant&#8221; based on experimental and/or theoretical evidence, and analyzed in terms of electronic, steric, thermodynamic, substitutional, or situational effects. Using these grids, students can predict and classify the likeliness of an H-bridge interaction between common organic molecules and understand their effects in more complex systems.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen Este artículo discute la formación de puentes de hidrógeno entre grupos funcionales con diversos grupos aceptores y OH donadores. Se presenta una serie de mallas circulares como ayuda visual para la organización y comparación de la diversidad de puentes de hidrógeno en moléculas orgánicas, haciendo énfasis en la presencia de un grupo OH (de alcoholes o fenoles, primordialmente) como donador de puente de hidrógeno. Los puentes de hidrógeno son clasificados como &#8220;poco probable&#8221;, &#8220;poco significativo&#8221; y &#8220;significativo&#8221;, de acuerdo con la evidencia experimental o teórica; y analizados en términos de efectos electrónicos, estéricos, termodinámicos, situacionales o de los sustituyentes. Nuestro objetivo es que el estudiante sea capaz de predecir y clasificar la probabilidad de interacción por puente de hidrógeno entre compuestos orgánicos comunes y comprender su efecto en sistemas más complejos.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Undergraduate]]></kwd>
<kwd lng="en"><![CDATA[Organic chemistry]]></kwd>
<kwd lng="en"><![CDATA[Hydrogen bonds]]></kwd>
<kwd lng="en"><![CDATA[H-bridges]]></kwd>
<kwd lng="en"><![CDATA[O-H donor groups]]></kwd>
<kwd lng="en"><![CDATA[Misconceptions]]></kwd>
<kwd lng="es"><![CDATA[Pre-grado]]></kwd>
<kwd lng="es"><![CDATA[Química orgánica]]></kwd>
<kwd lng="es"><![CDATA[Puentes de Hidrógeno]]></kwd>
<kwd lng="es"><![CDATA[Grupos donadores O-H]]></kwd>
<kwd lng="es"><![CDATA[Conceptos erróneos]]></kwd>
</kwd-group>
</article-meta>
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