Fundamentals7 QsFundamentals
Unattempted Aromaticity and Huckel's Rule
Apply Huckel's rule: count pi electrons, spot antiaromatic and nonaromatic rings, and track which lone pairs join the pi system.
Fundamentals10 QsFundamentals
Unattempted 1H and 13C NMR Basics
Count signals with symmetry, apply the n+1 splitting rule, and place chemical shifts for the common proton environments.
Pro
Cumulative ExamsPro20 QsCumulative Exams
Orgo 2 Final Exam
A comprehensive 20-question final exam covering all of Orgo 2: aromaticity and EAS, alcohols, ethers, and epoxides, carbonyl and carboxylic-acid derivative chemistry, enolates, amines and organometallics, and spectroscopy. Plan for about 35 minutes.
Reactions4 QsReactions
Unattempted Epoxide Reactions · Pt 1
Work through regioselective epoxide openings driven by acids, heteroatom nucleophiles, hydrides, and organometallic reagents
Reactions5 QsReactions
Unattempted Epoxide Reactions · Pt 2
Work through regioselective epoxide openings driven by acids, heteroatom nucleophiles, hydrides, and organometallic reagents
Reactions7 QsReactions
Unattempted Aldehyde and Ketone Reactions · Pt 1
Practice core aldehyde and ketone chemistry—reductions, nucleophilic additions, condensations, and Wittig-type transformations
Reactions5 QsReactions
Unattempted Aldehyde and Ketone Reactions · Pt 2
Practice core aldehyde and ketone chemistry—reductions, nucleophilic additions, condensations, and Wittig-type transformations
Reactions4 QsReactions
Unattempted Dienes: Conjugate Addition and Diels-Alder
Kinetic 1,2- vs thermodynamic 1,4-addition to conjugated dienes, plus Diels-Alder products, the s-cis requirement, and stereospecificity.
Reactions5 QsReactions
Unattempted EAS: Products and Directing Effects
Draw electrophilic aromatic substitution products and predict regiochemistry with activating, deactivating, and ortho/para vs meta directors.
Reactions6 QsReactions
Unattempted Carboxylic Acids and Derivatives
Interconvert the acyl family: acid chlorides, anhydrides, esters, and amides, with the reactivity order and reduction outcomes.