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<title>Organic Chemistry Laboratory Experiments</title>
<link href="http://hdl.handle.net/2144/1415" rel="alternate"/>
<subtitle/>
<id>http://hdl.handle.net/2144/1415</id>
<updated>2012-09-15T22:35:54Z</updated>
<dc:date>2012-09-15T22:35:54Z</dc:date>
<entry>
<title>Wittig Reaction</title>
<link href="http://hdl.handle.net/2144/2688" rel="alternate"/>
<author>
<name>Mulcahy, Seann P.</name>
</author>
<id>http://hdl.handle.net/2144/2688</id>
<updated>2012-01-17T07:00:30Z</updated>
<published>2012-01-03T00:00:00Z</published>
<summary type="text">Wittig Reaction
Mulcahy, Seann P.
A simple preparation of a conjugated diene via the olefination reaction between cinnamaldehyde and triphenylphosphonium chloride under basic conditions. Students are reintroduced to dry glassware techniques, recrystallization, and stereochemical determination by NMR. Modifications of this procedure include use of a Horner-Wadsworth-Emmons reagent or inclusion in a multi-step synthesis (ie. Diels-Alder reaction).
This work is licensed under a Creative Commons&#13;
Attribution-NonCommercial-ShareAlike 3.0 Unported License: http://creativecommons.org/licenses/by-nc-sa/3.0/
</summary>
<dc:date>2012-01-03T00:00:00Z</dc:date>
</entry>
<entry>
<title>Suzuki Cross Coupling</title>
<link href="http://hdl.handle.net/2144/2687" rel="alternate"/>
<author>
<name>Mulcahy, Seann P.</name>
</author>
<id>http://hdl.handle.net/2144/2687</id>
<updated>2012-01-17T07:00:29Z</updated>
<published>2012-01-03T00:00:00Z</published>
<summary type="text">Suzuki Cross Coupling
Mulcahy, Seann P.
An easy preparation of differentially-substituted biaryls is reported by palladium-catalyzed cross coupling. The Suzuki cross coupling reaction is both fast and substituent-independent. Column chromatography is performed to isolate pure biaryl product, which is analyzed by NMR.
This work is licensed under a Creative Commons&#13;
Attribution-NonCommercial-ShareAlike 3.0 Unported License: http://creativecommons.org/licenses/by-nc-sa/3.0/
</summary>
<dc:date>2012-01-03T00:00:00Z</dc:date>
</entry>
<entry>
<title>Fisher Esterification: Synthesis of Volatile Esters</title>
<link href="http://hdl.handle.net/2144/2686" rel="alternate"/>
<author>
<name>Mulcahy, Seann P.</name>
</author>
<id>http://hdl.handle.net/2144/2686</id>
<updated>2012-01-17T07:00:29Z</updated>
<published>2012-01-03T00:00:00Z</published>
<summary type="text">Fisher Esterification: Synthesis of Volatile Esters
Mulcahy, Seann P.
A microwave-accelerated synthesis of volatile aromatic esters is described in this convenient Fisher esterification reaction. Students perform a liquid-liquid extraction to isolate crude product which they purify by distillation. Analysis by GC/MS and NMR allows students to identify an unknown.
This work is licensed under a Creative Commons&#13;
Attribution-NonCommercial-ShareAlike 3.0 Unported License: http://creativecommons.org/licenses/by-nc-sa/3.0/
</summary>
<dc:date>2012-01-03T00:00:00Z</dc:date>
</entry>
<entry>
<title>Claisen-Schmidt (Aldol) Reaction</title>
<link href="http://hdl.handle.net/2144/2685" rel="alternate"/>
<author>
<name>Mulcahy, Seann P.</name>
</author>
<id>http://hdl.handle.net/2144/2685</id>
<updated>2012-01-17T07:00:28Z</updated>
<published>2012-01-03T00:00:00Z</published>
<summary type="text">Claisen-Schmidt (Aldol) Reaction
Mulcahy, Seann P.
A short aldol condensation reaction that produces differentially-substituted dibenzylideneketones whose UV-Vis spectra can be determined. This experiment allows students to construct structure-activity relationships in the context of the synthesis of a new sunscreen.
This work is licensed under a Creative Commons&#13;
Attribution-NonCommercial-ShareAlike 3.0 Unported License: http://creativecommons.org/licenses/by-nc-sa/3.0/
</summary>
<dc:date>2012-01-03T00:00:00Z</dc:date>
</entry>
</feed>
