Teaching GuideTerm Faculty of Science |
Mestrado en Investigación Química e Química Industrial |
Subjects |
Síntese estereoselectiva |
Learning aims |
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Identifying Data | 2015/16 | |||||||||||||
Subject | Síntese estereoselectiva | Code | 610509012 | |||||||||||
Study programme |
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Descriptors | Cycle | Period | Year | Type | Credits | |||||||||
Official Master's Degree | 1st four-month period |
First | Optativa | 3 | ||||||||||
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Learning outcomes | Study programme competences / results | ||
• Use of the terms and definitions of chemical reactivity, and the proper description of stereoselective reactions | AC1 |
BC10 |
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• Ability to use and communicate, both in written and oral forms, the basic concepts of dynamic stereochemistry in Organic Chemistry | BC2 BC4 BC10 |
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• Be familiar with the tridimensional representation of molecules, building the capacity to estimate their possible conformations. | BC1 BC2 BC3 BC7 BC10 |
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• Capacity to visualise molecular structures using models generated by quantum mechanical computations. | AC2 AC4 AC7 |
BC1 BC2 BC3 BC7 BC11 |
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• Understand the relationship between the tridimensional structure of the organic compounds and their reactivity | BC1 BC2 BC10 |
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• Understand the structural properties and the reactivity of the prostereogenic centers in those processes that generate new stereogenic elements. | AC1 |
BC1 |
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• Rationally explain the outcome of a chemical reaction in terms of the Stereochemistry | BC1 BC4 BC7 |
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• To know the main classes of reactions that generate stereocenters, and understand their mechanisms. | AC1 |
BC1 BC3 BC4 BC10 |
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• Understand the stereoelectronic effects and their role in chemical reactivity | AC1 |
BC1 BC4 BC5 |
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• Understand the value of the analysis of transition structures in chemical reactions, and be able to visualise those generated by quantum mechanical computations | AC2 AC4 AC7 |
BC1 BC2 BC3 BC7 BC11 |
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• Understand how the chirality of enantiopure compounds can be transmited to other chiral non-racemic products through chemical transformations | AC1 AC8 |
BC1 BC2 BC5 BC10 |
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• Quantity the relative ration of diastereoisomers and enantiomers using phisical and chemical methods. | AC1 |
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• Predict the outcome of a chemical reaction that generates novel stereocenters | AC1 |
BC1 |
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• Propose synthetic sequences for the preparation of chiral non-racemic molecules. | AC1 |
BC4 BC5 BC11 |
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• Acquire and utilize the existing literature on synthetic processes in which stereocenters are generated. | BC7 BC10 |
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