Appalachian State University
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Dernières notes et résumés Appalachian State University
explains how to determine acidity and defines acidity in 2 ways. diagrams how to assess stability of an acid's conjugate base.
Explains IUPAC nomenclature of alkanes, including how to name their substituents. Shows common conformations of ethane, propane, butane and cyclohexane along with their Newman projections and energy diagrams.
Shows 12 different mechanisms of reactions with alkenes, including how they are made. defines terms and provides reactants for each reaction.
Shows 12 different mechanisms of reactions with alkynes, including how alkynes are made. defines terms and provides reactants for each reaction.
includes some review of general chemistry topics and introduces what will be covered in organic. includes functional groups, a reaction masterlist, and several important key terms and concepts.
explains how chemical mechanisms work and shows diagrams with mechanism arrows drawn. Explains and diagrams 4 key mechanisms and defines key terms needed to understand mechanisms.
covers isomerism, goes into detail about how to identify stereoisomers of a compound. defines several key terms and has examples drawn out and explained. explains how chirality works and shows several examples
Notes taken on substitution and elimination reactions. Includes mechanisms, definitions, and reaction schemes for each type of reaction. Covers SN1, SN2, E1 and E2 reactions.
Part 2 of Chapter 7 of Organic Chemistry 1 at App State (CHE2201) taught by Dr. Moeller. This chapter is very long so it is split into two parts. The second part of this chapter covers elimination, Zaitsev's rule, hyperconjugation, regioselectivity, cis & trans alkenes, Newman projections, and rearrangements. Some images/definitions are not entirely my own; credit for any work that is not mine goes to its rightful owners.
Part 1 of Chapter 7 of Organic Chemistry 1 at App State (CHE2201) taught by Dr. Moeller. This chapter is very long so it is split into two parts. The first part of this chapter covers alkyl halide nomenclature, nucleophiles, substitution reactions (SN1 and SN2), reaction rates, leaving groups, solvents, and solvolysis. Some images/definitions are not entirely my own; credit for any work that is not mine goes to its rightful owners.