Organic reactions — summary sheet
Every reaction at a glance, grouped by type and drawn out (starting material → reagents → product). Tap any name for the full arrow‑pushing mechanism. Made to print as a study chart.
Searchable guide →Addition to C=C / C≡C
25 reactionsSomething adds across a π bond — Markovnikov or anti‑Markovnikov, syn or anti.
Elimination
6 reactionsLose two groups to make a π bond (E1 via carbocation, E2 concerted, Zaitsev vs Hofmann).
Substitution
45 reactionsOne group replaces another — Sₙ1/Sₙ2 at carbon, acyl substitution, and more.
Radical
6 reactionsSingle‑electron chains: initiation, propagation, termination.
Oxidation
21 reactionsGain C–O/C–X bonds or raise oxidation state (alcohols → carbonyls → acids).
Reduction
27 reactionsAdd H or remove O — hydride reagents, dissolving metal, catalytic H₂.
Carbonyl & enolate
36 reactionsNucleophiles add to (or α to) the C=O — addition, acyl substitution, enolate chemistry.
Organometallic
19 reactionsC–metal reagents forge C–C bonds: Grignard, organolithium, cuprate, Pd coupling.
Aromatic
8 reactionsReactions of the benzene ring — electrophilic (EAS) and nucleophilic (SNAr) substitution.
Pericyclic
7 reactionsConcerted, cyclic‑transition‑state reactions (Diels–Alder, sigmatropic shifts).
200 reactions across 10 types · Every reaction links to its step‑by‑step mechanism · Prefer to search or filter? Use the reaction guide.