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      <title>The Chemistry Of Amides by Ale Chavez</title>
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      <language>en-us</language>
      <pubDate>2022-05-18 22:26:09 UTC</pubDate>
      <lastBuildDate>2022-05-19 00:27:10 UTC</lastBuildDate>
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         <title>What is Amide?</title>
         <author>alechavez573</author>
         <link>https://padlet.com/alechavez573/cm44c4bw6mvztvzr/wish/2190254268</link>
         <description><![CDATA[<div>Amides are regarded as derivatives of carboxylic acids in which the hydroxyl group has been replaced by an amine or ammonia. In the typical nomenclature, the term amide is added to the stem of the parent acid's name – the simplest amide derived from acetic acid is acetamide (CH<sub>3</sub>CONH<sub>2</sub>).</div>]]></description>
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         <pubDate>2022-05-18 22:55:55 UTC</pubDate>
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         <title>What is the function of amide?</title>
         <author>alechavez573</author>
         <link>https://padlet.com/alechavez573/cm44c4bw6mvztvzr/wish/2190257364</link>
         <description><![CDATA[<div>In primary and secondary amides, the presence of N–H dipoles allows amides to function as H-bond donors as well. Thus amides can participate in hydrogen bonding with water and other protic solvents; the oxygen atom can accept hydrogen bonds from water and the N–H hydrogen atoms can donate H-bonds.</div>]]></description>
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         <pubDate>2022-05-18 23:00:27 UTC</pubDate>
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         <title>Common Reactions</title>
         <author>alechavez573</author>
         <link>https://padlet.com/alechavez573/cm44c4bw6mvztvzr/wish/2190311706</link>
         <description><![CDATA[<div>The characteristic reaction of covalent amides is hydrolysis (a chemical reaction with water), by which they are converted to acids and amines; this reaction ordinarily is slow unless it is catalyzed by a strong acid, an alkali, or an enzyme. Amides also can be dehydrated to nitriles.</div>]]></description>
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         <pubDate>2022-05-19 00:06:37 UTC</pubDate>
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         <title>Interesting Facts</title>
         <author>alechavez573</author>
         <link>https://padlet.com/alechavez573/cm44c4bw6mvztvzr/wish/2190314294</link>
         <description><![CDATA[<div>1. Amides also can be dehydrated to nitriles. Amides are not readily oxidized nor reduced, although hydrogenation (addition of hydrogen at high temperatures and pressures) in the presence of a catalyst will convert most amides of carboxylic acids to amines.<br>2.Amides may be used to form resilient structural materials. Dimethylformamide is an important organic solvent. Plants produce amides for a variety of functions. Amides are found in many drugs.<br>3.Amides represent a very important functional group in organic chemistry and find a wide variety of use, especially in living systems and medicines that many people depend on.</div>]]></description>
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         <pubDate>2022-05-19 00:09:18 UTC</pubDate>
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         <title>Structures</title>
         <author>alechavez573</author>
         <link>https://padlet.com/alechavez573/cm44c4bw6mvztvzr/wish/2190317817</link>
         <description><![CDATA[<div>Amides have a general structure in which <strong>a nitrogen atom is bonded to a carbonyl carbon atom</strong>. In names for amides, the -ic acid of the common name or the -oic ending of the IUPAC for the corresponding carboxylic acid is replaced by -amide.</div>]]></description>
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         <pubDate>2022-05-19 00:12:28 UTC</pubDate>
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         <title>Physical Properties</title>
         <author>alechavez573</author>
         <link>https://padlet.com/alechavez573/cm44c4bw6mvztvzr/wish/2190319639</link>
         <description><![CDATA[<div><strong>Formamide is a liquid while all other amides are colourless, crystalline at room temperature.</strong> The lower aliphatic amide are quite soluble in water. The solubility decreases with the increase in size of alkyl groups. The melting and boiling points of amides are higher than expected.</div>]]></description>
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         <pubDate>2022-05-19 00:14:12 UTC</pubDate>
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         <title></title>
         <author>alechavez573</author>
         <link>https://padlet.com/alechavez573/cm44c4bw6mvztvzr/wish/2190320891</link>
         <description><![CDATA[]]></description>
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         <pubDate>2022-05-19 00:15:23 UTC</pubDate>
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         <title></title>
         <author>alechavez573</author>
         <link>https://padlet.com/alechavez573/cm44c4bw6mvztvzr/wish/2190321460</link>
         <description><![CDATA[]]></description>
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         <pubDate>2022-05-19 00:15:55 UTC</pubDate>
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         <title></title>
         <author>alechavez573</author>
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         <description><![CDATA[]]></description>
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         <pubDate>2022-05-19 00:16:16 UTC</pubDate>
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         <title>References</title>
         <author>alechavez573</author>
         <link>https://padlet.com/alechavez573/cm44c4bw6mvztvzr/wish/2190323105</link>
         <description><![CDATA[<div>https://en.wikipedia.org/wiki/Amide<br>https://www.oxfordreference.com/view/10.1093/oi/authority.20110803095408455<br>https://www.jpharmsci.org/article/S0022-3549(15)35625-2/references<br>https://www.masterorganicchemistry.com/2018/02/28/amides-properties-synthesis-and-nomenclature/</div>]]></description>
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         <pubDate>2022-05-19 00:17:32 UTC</pubDate>
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         <title></title>
         <author>alechavez573</author>
         <link>https://padlet.com/alechavez573/cm44c4bw6mvztvzr/wish/2190325626</link>
         <description><![CDATA[]]></description>
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         <pubDate>2022-05-19 00:19:47 UTC</pubDate>
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