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<title>OCR AS Chemistry</title>
<link>http://www.sutsci.org/ocras/</link>
<description></description>
<dc:language>en-us</dc:language>
<dc:creator></dc:creator>
<dc:date>2010-05-15T20:30:34+00:00</dc:date>
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<item rdf:about="http://www.sutsci.org/ocras/archives/000622.html">
<title>Alcohols</title>
<link>http://www.sutsci.org/ocras/archives/000622.html</link>
<description>These compounds contain the -OH functional group. There is a school of thought that includes water in this category, since this too contains the -OH group. I leave it to you to decide whether to subscribe to this ideal, but...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2010-05-15T20:30:34+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000862.html">
<title>F322 specimen examination</title>
<link>http://www.sutsci.org/ocras/archives/000862.html</link>
<description>Please look at this ... and try it... Download file...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-12-10T13:58:00+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000641.html">
<title>Oxidation and Reduction</title>
<link>http://www.sutsci.org/ocras/archives/000641.html</link>
<description>Oxidation can be defined as a reaction in which atoms react with oxygen [well THAT figures!] but this definition is far too unrefined! Many reactions that do not involve oxygen at all may still be classified as involving oxidation. To...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-11-16T23:23:27+00:00</dc:date>
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<item rdf:about="http://www.sutsci.org/ocras/archives/000849.html">
<title>spectroscopy slides...</title>
<link>http://www.sutsci.org/ocras/archives/000849.html</link>
<description>...here they are. Enjoy! Download file...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-10-24T13:10:50+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000848.html">
<title>message board...</title>
<link>http://www.sutsci.org/ocras/archives/000848.html</link>
<description>... just a reminder that a message board exists for general chat / questions / comments etc. Go to http://www.bodmas.org/vanilla/ and apply for memebership This is a private site for my students , no one else. Your comments will therefore...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-10-22T14:27:54+00:00</dc:date>
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<item rdf:about="http://www.sutsci.org/ocras/archives/000843.html">
<title>Periodic Table [good]</title>
<link>http://www.sutsci.org/ocras/archives/000843.html</link>
<description>Worth putting into your favourites box... http://www.ptable.com...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-10-12T09:29:59+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000842.html">
<title>First Test</title>
<link>http://www.sutsci.org/ocras/archives/000842.html</link>
<description>Please note that the half term test will take place during week beginning 12th October. This will consist of a set of short answer structured questions that will be answered on the test paper. The content will be based on...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-10-12T09:27:24+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000621.html">
<title>It&apos;s reagent types, init?</title>
<link>http://www.sutsci.org/ocras/archives/000621.html</link>
<description>These notes were originally put onto the A2 site...but you might as well hear them here! Click on the &quot;posted by&quot; line......</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-10-12T08:33:00+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000628.html">
<title>Haloalkanes</title>
<link>http://www.sutsci.org/ocras/archives/000628.html</link>
<description>The haloalkanes represent an extremely versatile group of molecules which would be well worth taking with you onto your desert island...should you ever find yourself marooned. The polar bond introduced with the appearance of the halogen atom gives the carbon...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-10-12T08:32:48+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000629.html">
<title>more on alcohols...</title>
<link>http://www.sutsci.org/ocras/archives/000629.html</link>
<description>Alcohols can suffer dehydration reactions as well as oxidation. However, an important difference is that ALL classes of alcohols, including tertairy, can be deydrated, although of course tertiary ones cannot be oxidised. The reagent is concentrated sulphuric acid, but the...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-10-12T08:31:15+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000783.html">
<title>Mechanisms</title>
<link>http://www.sutsci.org/ocras/archives/000783.html</link>
<description>A few slides for your review..... Download file...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-09-29T19:41:40+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000831.html">
<title>name them...</title>
<link>http://www.sutsci.org/ocras/archives/000831.html</link>
<description>3,4,5-trimethyl nonane cis-3,4-dimethyldec-3-ene 4-chloro-nonan-1-ol hexan-3-one octanoic acid 3-bromopentanal 3-hydroxy-2-methylheptanal...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-09-27T16:41:59+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000613.html">
<title>isomer numbers...</title>
<link>http://www.sutsci.org/ocras/archives/000613.html</link>
<description>The number of structural isomers that can be produced rises rapidly with the number of carbon atoms.. for example, the alkane with 4 carbon atoms has 2 isomers; the one with 7 has 9 structures ...C 10 has 75...and C20......</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-09-25T21:37:00+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000620.html">
<title>There&apos;s more to alkenes than meets the eye...</title>
<link>http://www.sutsci.org/ocras/archives/000620.html</link>
<description>Alkenes undergo electrophilic addition reactions, but with certain alkenes the question of orientation of addition arises. With the reaction of propene with hydrogen bromide, what will be the major product since two possibilities exist: 1-bromopropane and 2-bromopropane. Alkenes can be...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-09-25T21:32:08+00:00</dc:date>
</item>
<item rdf:about="http://www.sutsci.org/ocras/archives/000614.html">
<title>electrophiles, nucleophiles...and more!</title>
<link>http://www.sutsci.org/ocras/archives/000614.html</link>
<description>Organic reactions are often classified using two words: one identifying the type of REAGENT and the other the type of REACTION. Nucleophiles are electron pair donors, which use that pair to form a new bond to the substrate. If you...</description>
<dc:subject></dc:subject>
<dc:creator>dcox</dc:creator>
<dc:date>2009-09-25T21:30:09+00:00</dc:date>
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