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This course is a continuation of CHEM103 [1]: Organic Chemistry I. As you progress through the units below, you will continue to learn the different chemical reactions characteristic of each family of organic compounds. We will focus on four most important classes of reactions: electrophilic substitution at aromatic rings, nucleophilic addition at carbonyl compounds, hydrolysis of carboxylic acids, and carbon-carbon bond formation using enolates. The enolate portion of this course will cover the reactivity of functional groups. We will also look at synthetic strategies for making simple, small organic molecules, using the knowledge of organic chemistry accumulated thus far. At the end of this course, you will possess the tools you need to plan the synthesis of fairly complicated molecules, like those used in pharmaceutics. From the perspective of a synthetic organic chemist, the two most challenging aspects of synthesizing drug molecules are the incorporation of "molecular rings" (rings of 5, 6,… Categories:
Life Sciences
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AlternativesIf you know any alternatives, please let us know. PrerequisitesIf you can suggest any prerequisite, please let us know. Certification Exams-- there are no exams to get certification after this course --If your company does certification for those who completed this course then register your company as certification vendor and add your exams to the Exams Directory. | ||
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