Carleton University| Isolation and Reactions of Cholesterol| S10-CHEM 2203 lump science lab account statement| Emily Giroux: 100-688-773| Lab partner: Sarah Heinzle| TA: Jamie Davey| 5/26/2010| 4-cholesten-3-one (C27H45O) was synthesized from its cholesterin (C27H45OH) herald by consecutive brominating, oxidizing, debrominating, and isomerizing the intricate to produce cholesterol dibromide, dibromocholestanone, 5-cholesten-3-one and 4-cholesten-3-one. Recrystallization and FT-IR spectrum compend were the main techniques use to purify and confirm personal identity and probity of the deepens, respectively. Functional host characterization by FT-IR spectra analysis of the 5-cholesten-3-one and 4-cholesten-3-one standards resembled the literature spectra of the pure compounds. The 5 cholesten-3-one and 4-cholesten-3-one experiment spectra produced absorbance peaks from 3000-2800cm-1 mark of their cytosine systema skeletale and hydrocarbon tail. The 5-cholesten-3-one sample spectra also feature mainpeaks at 1718cm-1 and 1468cm-1, indicative of the compounds un fuse ketone and olefine bond, respectively. The 4-cholesten-3-one sample spectra produced absorbance peaks at 1677cm-1 and 1466cm-1, characteristic of the compounds joined ketone and alkene bond, respectively.
The minor front of the hydroxyl functional chemical group was noted in the 5-cholesten-3-one sample spectra, and of conjugated and unconjugated ketone groups in the 5-cholesten-3-one and 4-cholesten-3-one sample spectra, respectively. The recovery of 5-cholesten-3-one from cholesterol was 18.9%. This deliver was significantly affected by the loss of product imputable to a spill during the debromination process. The recovery of 4-cholesten-3-one from 5-cholesten-3-one was 82.7%. The FT-IR spectra obtained for the sample compounds confirmed that the reactions apply passim the synthesis of 4-cholesten-3-one were successful. | Introduction The purpose of this...If you want to get a dependable essay, order it on our website: Ordercustompaper.com
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