CHE 2202 (CHE2202)
Appalachian State University
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Organic Chem 2 study pack
Notes from organic chemistry 2. Covers reactions of several functional group families, including oxygen containing groups and aromatic compounds. Nomenclature is included for each group as well.
Class notes
Aromatic substitution reactions
Mainly discusses electrophilic aromatic substitution but mentions nucleophilic reactions as well. Explains and defines activators and deactivators in terms of reactivity. Talks about sulfonation, nitration, Friedel Crafts alkylation and acylation, and halogenation reactions of aromatic compounds.
Class notes
Spectroscopy
Explains uses of mass spectrometry, NMR, and IR spectroscopy. Explains features of each method’s data, and how to read the spectra to determine structure of a molecule.
Class notes
Conjugated pi systems and pericyclic reactions
Discusses how conjugation works, and how it affects stability and reactivity of a molecule. Includes information about nomenclature, and shows how pericyclic reactions work, including their mechanisms. The diels alder reaction is focused on.
Class notes
Ethers and epoxides
Discusses nomenclature, preparation and reactions of ether and epoxide compounds.
Summary
Carboxylic acids and derivatives
Carboxylic acids and derivatives
Class notes
Carboxylic acids and derivatives
Discusses nomenclature, reactions and mechanisms of carboxylic acids and their derivatives. This includes nitriles, amides, acyl halides, esters and anhydrides. Goes over preparation and reaction of all derivatives, as well as their relative reactivity.
Class notes
aromatic compounds and benzene derivatives
goes over nomenclature of aromatic compounds and benzene derivatives, including common names. Also includes synthesis and reactions of aromatics. Defines aromaticity as well.
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aldehydes and ketones (carbonyl compounds)
goes over nomenclature of carbonyl compounds, including aldehydes and ketones. Also goes over synthesis and reactions of these compounds.
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Alcohols
Goes over nomenclature, reactions and mechanisms of alcohols.