<?xml version="1.0"?>
<rss version="2.0">
   <channel>
      <title>Chapter 7 Alkynes by </title>
      <link>https://padlet.com/s65333/535ysgk07ibw3ufr</link>
      <description></description>
      <language>en-us</language>
      <pubDate>2023-01-14 10:04:50 UTC</pubDate>
      <lastBuildDate>2023-01-14 15:36:21 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
      <image>
         <url></url>
      </image>
      <item>
         <title>structure alkynes</title>
         <author>s65333</author>
         <link>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444338837</link>
         <description><![CDATA[<div><br>&gt;contain carbon-carbon triple bond.<br>&gt;consists of 2 pi bond and 1 sigma bond.</div>]]></description>
         <enclosure url="https://www.lifeder.com/wp-content/uploads/2021/04/enlace-covalente-triple-concepto-1024x898.jpg" />
         <pubDate>2023-01-14 14:06:49 UTC</pubDate>
         <guid>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444338837</guid>
      </item>
      <item>
         <title>Naming of alkynes</title>
         <author>s65333</author>
         <link>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444339680</link>
         <description><![CDATA[<div><br>&gt;IUPAC system,change from -ane ending of parent name to -yne for alkynes.&nbsp;<br>&gt;choose longest continuous chain and number chain to give the triple bond the lower number.&nbsp;<br>&gt;the chain is numbered to give the first site of saturation the lower number.&nbsp;<br>(two triples bond-diynes,&nbsp;<br>three triples bond-triyes)</div>]]></description>
         <enclosure url="http://image3.slideserve.com/6635242/naming-alkynes-n.jpg" />
         <pubDate>2023-01-14 14:09:05 UTC</pubDate>
         <guid>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444339680</guid>
      </item>
      <item>
         <title>Preparation of alkynes</title>
         <author>s65333</author>
         <link>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444340531</link>
         <description><![CDATA[<div><br>prepared by elimination reactions,a strong base removes two equivalents of Hx form a vicinal or geminal dihalide to yield an alkynes through two successive E2 elimination reaction.<br>(Hx,x=Cl,Br,I)</div>]]></description>
         <enclosure url="https://image.slidesharecdn.com/11-140930102017-phpapp02/95/115-preparation-of-alkynes-2-638.jpg?cb=1412072683" />
         <pubDate>2023-01-14 14:11:40 UTC</pubDate>
         <guid>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444340531</guid>
      </item>
      <item>
         <title>Cyclic alkynes</title>
         <author>s65333</author>
         <link>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444341344</link>
         <description><![CDATA[<div><br>unstable : carbon chain must be long enough to connect the two ends of the triple bond without introducing too much strain.</div>]]></description>
         <enclosure url="http://www.sliderbase.com/images/referats/147b/(8).PNG" />
         <pubDate>2023-01-14 14:13:52 UTC</pubDate>
         <guid>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444341344</guid>
      </item>
      <item>
         <title>What is ALKYNES??</title>
         <author>s65333</author>
         <link>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444342119</link>
         <description><![CDATA[]]></description>
         <enclosure url="http://4.bp.blogspot.com/-wx10Q_nvkZg/Ut7mIXqtl9I/AAAAAAAAC_0/Zf4kXNdh63M/s1600/Think-Differently.jpg" />
         <pubDate>2023-01-14 14:16:06 UTC</pubDate>
         <guid>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444342119</guid>
      </item>
      <item>
         <title>Strength of ALKYNES bonds:</title>
         <author>s65333</author>
         <link>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444351220</link>
         <description><![CDATA[<div>&gt;sp hybridized with linear geometry and bond angles of 180 -unsaturated hydrocarbon.<br>&gt;when sigma bond more bigger than pi bond so the triple bond more easily broken.&nbsp;<br>&gt;alkynes are more polarized than alkenes because electron more losely held.&nbsp;</div>]]></description>
         <enclosure url="https://qph.fs.quoracdn.net/main-qimg-43aa015750c32e2c654348e6fd890620" />
         <pubDate>2023-01-14 14:40:36 UTC</pubDate>
         <guid>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444351220</guid>
      </item>
      <item>
         <title>Physical properties</title>
         <author>s65333</author>
         <link>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444353721</link>
         <description><![CDATA[<div><br>&gt;resemble those of hydrocarbons of similar shape and molecular weight.&nbsp;<br>&gt;melting points and boiling points increases when the number of carbon increases.&nbsp;<br>&gt;soluble in organic solvent and insoluble in water.</div>]]></description>
         <enclosure url="" />
         <pubDate>2023-01-14 14:47:40 UTC</pubDate>
         <guid>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444353721</guid>
      </item>
      <item>
         <title>addition reactions of alkenes</title>
         <author>s65333</author>
         <link>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444354103</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://www.chemistrylearner.com/wp-content/uploads/2020/03/Addition-Reaction-Alkene-Examples.jpg" />
         <pubDate>2023-01-14 14:48:46 UTC</pubDate>
         <guid>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444354103</guid>
      </item>
      <item>
         <title>synthesis using ALKYNES</title>
         <author>s65333</author>
         <link>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444360721</link>
         <description><![CDATA[<div>&gt;to consider HOW to prepare a five-carbon product from three smaller precursor molecules using the reaction.</div>]]></description>
         <enclosure url="https://image1.slideserve.com/2978916/synthesis-of-alkynes-l.jpg" />
         <pubDate>2023-01-14 15:05:38 UTC</pubDate>
         <guid>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444360721</guid>
      </item>
      <item>
         <title>Internal vs Terminal ALKYNES </title>
         <author>s65333</author>
         <link>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444372982</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1933159728/0c4261efc22efcc8b89cc2b2ec30ded4/Screenshot_20230114_233314_PowerPoint.jpg" />
         <pubDate>2023-01-14 15:35:17 UTC</pubDate>
         <guid>https://padlet.com/s65333/535ysgk07ibw3ufr/wish/2444372982</guid>
      </item>
   </channel>
</rss>
