Chemistry and Biochemistry
 

Organic Chemistry 2

Organic Chemistry 2
Emphasis on organic reactions, reaction mechanisms, synthesis, and spectroscopy building on the foundation of Chem 351, including carbonyl chemistry, and chemistry of aromatic compounds, organic acids and bases, polymers, and biomolecules.
CHEM
352
 Hours3.0 Credit, 3.0 Lecture, 1.0 Lab
 PrerequisitesCHEM 351; or CHEM 351M
 NotePrimarily for majors in chemical engineering and the biological sciences.
 TaughtFall, Winter, Spring, Summer
 ProgramsContaining CHEM 352
Course Outcomes: 

Predict Structure and Reactivity

Predict structure and reactivity of aldehydes, ketones, carboxylic acids, esters, anhydrides, amides, b-ketocarbonyl containing compounds, amines, and phenols.

Curved Arrow Mechanisms

Recognize and provide curved arrow mechanisms for the following types of organic reactions: electrophilic & nucleophilic aromatic substitution, nucleophilic carbonyl addition, nucleophilic acyl substitution, carbonyl condensation, [4 2] cycloaddition, and substitution ato a carbonyl.

Recognize and Predict Reactivity

Recognize and predict the reactivity of the following reactive species and/or reactive intermediates: Grignard reagents, Wittig reagents, organolithiums, diorganocuprates, enols, enolates, aryl diazonium ions, and benzynes.

Recognize and Predict Structure/Reactivity

Recognize and predict the structure and reactivity of the following classes of biologically important organic molecules: carbohydrates, amino acids, proteins, and lipids.