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      <title>Organic Naming by </title>
      <link>https://padlet.com/lana_brown/ws64b1wwn7qz</link>
      <description>Graphic Organizer of Organic Naming in Chemistry.</description>
      <language>en-us</language>
      <pubDate>2018-09-10 12:27:23 UTC</pubDate>
      <lastBuildDate>2018-09-11 02:15:03 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>Organic Compounds </title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279361824</link>
         <description><![CDATA[<div>Contain at least one Carbon.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 12:32:06 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279361824</guid>
      </item>
      <item>
         <title>Hydrocarbons</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279361948</link>
         <description><![CDATA[<div>Are organic compounds that only contain a carbon and hydrogen.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 12:32:21 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279361948</guid>
      </item>
      <item>
         <title>Hydrocarbon Naming</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279364645</link>
         <description><![CDATA[<div>Named by their structure. The simplest group being the Alkanes.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 12:37:57 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279364645</guid>
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      <item>
         <title>Named by longest chain of carbon</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279594802</link>
         <description><![CDATA[<div>The chain names along with there numbers include;<br>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 Dec...<br>The longest chain may be bent.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 19:38:51 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279594802</guid>
      </item>
      <item>
         <title>Alkane Endings</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279596155</link>
         <description><![CDATA[<div>All Alkanes end in -ANE.<br><br>Example; one carbon would be called MethANE.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 19:42:22 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279596155</guid>
      </item>
      <item>
         <title>Substituents</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279606638</link>
         <description><![CDATA[<div>Once the longest chain is located all the other chains of carbon attached to it are called substituents.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 20:16:14 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279606638</guid>
      </item>
      <item>
         <title>Naming Substituents </title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279606999</link>
         <description><![CDATA[<div>All substituents are have the ending of -YL after the stem. <br><br>Example; MethYL.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 20:17:25 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279606999</guid>
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      <item>
         <title>Naming Substituents</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279617162</link>
         <description><![CDATA[<div>If there are more than one substituent of the same kind you would use a prefix to indicate how many there are.<br>Prefixes;<br>1 has no prefix<br>2 di...<br>3 tri...<br>4 tetra...<br>etc.<br><br>Example; If there are three methyl substituents then the name would be TRImethyl</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 20:39:30 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279617162</guid>
      </item>
      <item>
         <title>Substituent Order</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279620310</link>
         <description><![CDATA[<div>Substituents should be named in alphabetical order to keep the name understood for everyone.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 20:53:06 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279620310</guid>
      </item>
      <item>
         <title>Cyclic Chain</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279632372</link>
         <description><![CDATA[<div>This formation is prefixed with the word CYCLO...<br><br>Substituents in this formation are treated the same as one on a chain.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 21:50:51 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279632372</guid>
      </item>
      <item>
         <title>Alkenes</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279635083</link>
         <description><![CDATA[<div>Double carbon bonds have the ending of -ENE. <br><br>Example; EthENE.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 22:07:01 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279635083</guid>
      </item>
      <item>
         <title>Alkenes and Alkynes</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279636186</link>
         <description><![CDATA[<div>The number of carbon that the double bond is located on is the number used to indicate.<br><br>Example; c=c-c-c=c-c-c<br>1,4-heptene</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 22:15:02 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279636186</guid>
      </item>
      <item>
         <title>Cis and Trans</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279637122</link>
         <description><![CDATA[<div>Cis is when like groups of atoms are on the same side of the Alkene compound.<br><br>Trans is when these like groups are on opposite sides of the compound.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 22:21:59 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279637122</guid>
      </item>
      <item>
         <title>Alkynes</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279637965</link>
         <description><![CDATA[<div>Triple carbon bonds have the ending of -YNE.<br><br>Example; PropYNE.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 22:28:47 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279637965</guid>
      </item>
      <item>
         <title>Aromatic Hydrocarbons</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279638281</link>
         <description><![CDATA[<div>Made up of a strong ring of six carbons. The parent is called Benzene. <br><br>Example;<br>   c<br> // \<br>c    c-c<br>|     ||<br>c    c<br> \\ /<br>   c<br>Methylbenzene.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 22:31:24 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279638281</guid>
      </item>
      <item>
         <title>Alcohols</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279639132</link>
         <description><![CDATA[<div>Alcohols have the ending of -OL. They contain (OH).<br>The numbering system still applies to alcohols.</div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 22:37:21 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279639132</guid>
      </item>
      <item>
         <title>Organic Acids</title>
         <author>lana_brown</author>
         <link>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279640223</link>
         <description><![CDATA[<div>The formula is (COOH).<br>In naming these you take off the final 'e' in the ending of alkanes and add -OIC. </div>]]></description>
         <enclosure url="" />
         <pubDate>2018-09-10 22:44:43 UTC</pubDate>
         <guid>https://padlet.com/lana_brown/ws64b1wwn7qz/wish/279640223</guid>
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