<?xml version="1.0"?>
<rss version="2.0">
   <channel>
      <title>Organic Naming Mind Map by Megi Lika</title>
      <link>https://padlet.com/likamegi001/88zntw1n7ca4</link>
      <description>By: Arden &amp; Megi </description>
      <language>en-us</language>
      <pubDate>2018-09-09 21:54:24 UTC</pubDate>
      <lastBuildDate>2025-10-25 15:51:32 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
      <image>
         <url></url>
      </image>
      <item>
         <title>Naming  </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279206404</link>
         <description><![CDATA[<div>1 - Meth <br>2 - Eth <br>3 - Prop <br>4 - But <br>5 - Pent <br>6 - Hex<br>7 - Hept <br>8 - Oct <br>9 - Non<br>10 - Deca<br><br><mark>Alkanes have -ANE ending <br><br></mark>*Click on image to view example* </div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/283976371/48aed293de6d533f98c4b458f5d64842/Screen_Shot_2018_09_11_at_9_47_17_AM.png" />
         <pubDate>2018-09-09 22:01:19 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279206404</guid>
      </item>
      <item>
         <title>Alkanes </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279206623</link>
         <description><![CDATA[<div>Simplest group of hydrocarbons is called Alkanes <br><br><mark>-ANE ending  <br>Indicates a single bond <br></mark><br>***Each carbon has 4 bonds and each hydrogen has 1 bond</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/283976371/e96438a2d4c2b6d6bb8c8c872662f5e5/Screen_Shot_2018_09_11_at_10_05_16_AM.png" />
         <pubDate>2018-09-09 22:03:06 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279206623</guid>
      </item>
      <item>
         <title>Naming Substituents </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279211239</link>
         <description><![CDATA[<div>Substituents are named by adding -<mark>YL</mark> to the stem on how many carbons are attached </div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-09 22:57:43 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279211239</guid>
      </item>
      <item>
         <title>Substituents </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279211444</link>
         <description><![CDATA[<div>All groups attached to the longest chain are called substituents (meaning groups) <br><br>To indicate which carbon these groups are attached to we # the carbons in the longest chain.<br><br>-An easy way to remember what substituents are is to think of them as "arms" branching off the longest chain!</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-09 23:00:00 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279211444</guid>
      </item>
      <item>
         <title>Multiple Substituents </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279211520</link>
         <description><![CDATA[<div>When 2 or more of the substituents in a formula are alike a prefix is used <br>2 - Di <br>3 - Tri <br>4 - Tetra <br>5 - Penta <br>6 - Hexa <br>7 - Hepta <br>8 - Octo <br>9 - Nona <br>10 - Deca <br><br>These are added to the substituent name to indicate the correct multiplicity </div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-09 23:00:49 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279211520</guid>
      </item>
      <item>
         <title>Alkenes </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279211821</link>
         <description><![CDATA[<div>Unsaturated hydrocarbons <mark>-ENE ending <br>Indicates double bond<br><br></mark>When determining the longest possible chain the&nbsp; double bond must be included<br><br>*Click on image to view example*&nbsp;</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/283976371/9ac9d4a38812f8f3d19c383f54125d78/Screen_Shot_2018_09_11_at_10_11_20_AM.png" />
         <pubDate>2018-09-09 23:04:39 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279211821</guid>
      </item>
      <item>
         <title>Alkynes </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279211866</link>
         <description><![CDATA[<div>*** Same as alkenes for naming but ending is different <br><br><mark>-YNE ending <br>Indicates triple bond<br><br></mark>*Click on image to view example* </div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/283976371/3556a03dd4787f5f7b14d6940afe0663/Screen_Shot_2018_09_11_at_10_13_24_AM.png" />
         <pubDate>2018-09-09 23:05:19 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279211866</guid>
      </item>
      <item>
         <title>Cis </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279212229</link>
         <description><![CDATA[<div>Isomer with like groups or atoms on the <strong>same</strong> side on the alkene linkage <br><br>If "cis" applies; insert in the beginning of the naming. <br><br>*Click on image to view example* </div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/283976371/dae204659907a1efbfd449761b596502/Screen_Shot_2018_09_11_at_9_54_43_AM.png" />
         <pubDate>2018-09-09 23:07:59 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279212229</guid>
      </item>
      <item>
         <title>Trans </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279212345</link>
         <description><![CDATA[<div>Isomer with like group of atoms on the <strong>opposite</strong> side of the alkene linkage<br><br>If "trans" applies; insider in the beginning of the naming.  <br><br>*Click on image to view example*</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/283976371/0617609854a6afa89555f32c2d996420/Screen_Shot_2018_09_11_at_9_55_34_AM.png" />
         <pubDate>2018-09-09 23:08:39 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279212345</guid>
      </item>
      <item>
         <title>Cyclo </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279212623</link>
         <description><![CDATA[<div>- Ring formation <br>- When the chain is in the form of a shape <br><br>Add in <mark>cyclo</mark> in the name <br>*Click on image to view example*</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/283976371/60a26cefd64c2984130e214ed0ce3039/organic_chemistry_.png" />
         <pubDate>2018-09-09 23:11:41 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279212623</guid>
      </item>
      <item>
         <title>Aromatic </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279213325</link>
         <description><![CDATA[<div>- Hydrocarbons <br><br>Built for extremely stable six atom carbon ring <br>Parent aromatic is called <strong>benzene </strong>(base name) <br><br>*Click on image to view example*</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/283976371/a063921e431e41ea4bed491da8983aaa/Screen_Shot_2018_09_09_at_7_23_03_PM.png" />
         <pubDate>2018-09-09 23:18:42 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279213325</guid>
      </item>
      <item>
         <title>Visual Example of Bonds</title>
         <author>stabarde289</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279226032</link>
         <description><![CDATA[<div>*Click image to view how single, double and triple bonds are represented(right side)*</div>]]></description>
         <enclosure url="http://surfguppy.com/wp-content/uploads/2014/04/CARBON-TO-ARBON-BONDS.jpg" />
         <pubDate>2018-09-10 01:00:42 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279226032</guid>
      </item>
      <item>
         <title>Introduction </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279853065</link>
         <description><![CDATA[<div>Organic chemistry is the study of compounds of carbon. <br>Carbon combines with elements such as: H, O, N, Cl, Br and S. </div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-11 13:42:34 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279853065</guid>
      </item>
      <item>
         <title>Numbering </title>
         <author>likamegi001</author>
         <link>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279857827</link>
         <description><![CDATA[<div>You can number the chain from either end but the rule is to number the chain from the end that will have the least possible number</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-11 13:50:18 UTC</pubDate>
         <guid>https://padlet.com/likamegi001/88zntw1n7ca4/wish/279857827</guid>
      </item>
   </channel>
</rss>
