Stereochemistry of Bromobutane Enantiomers

Jun 29th, 2015
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Fairleigh Dickinson University
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Introduction; Abstract; Procedures; Results; Discussion; Review Question Answer Key

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Tam HoLab Partner: Urusha LamaNov 7, 13STRUCTURE & NOMENCLATUREI. AbstractSince there thousands of different organic compounds with distinctive structures, being able to acknowledge each compound three-dimensional structure and name is very essential. To systemize organic compound names, IUPAC system of nomenclature is used (devised in 1892). In today's lab, we used models to experiment with different ways a molecule can be put together.We build isomer models and come up with IUPAC names based upon the structures for each concise formula. The order is C5H12 , C4H9Cl for enantiomers structures and 2,3-dibromobutane for diastereomer structure.Based on the basic property of chiral center (having 4 different substituents), we experiment different way of building molecule models of the same molecular formula.For drawing the structure, I use an online application which can be accessed via http://www.emolecules.com/ II. Results and DiscussionFor C5H12, there are 3 chain isomers. However, one of the isomers also have its own enantiomers.n-pentane 2,2-dimethyl propane~~~~2-methylbutane(S)-2-methylbutane(R)-2-methylbutaneC4H9Cl1-chlorobutane2-chloro-2-methylpropane1-chloro-2-methylpropane(R)-2-chlorobutane(S)-2-chlorobutaneThese enantiomers are non-superimposable and each is mirror image to the other.2,3-dibromobutane(2R,3R)-2,3-dibromobutane(2S,3R)-2,3-dibromobutane(2R,3R)-2,3-dibromobutane(2S,3R)-2,3-dibromobutane 2,3-dibromobutane

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