Alkyl Halides
- Alkyl Halide Reactions: Carboxylic Acid formation using Alkyl Halides, Mg, and CO2
- Alkyl Halide Reactions: Alkene formation using Bulky Bases (E2 Hofmann Product)
- Alkyl Halide Reactions: Alkene formation using Strong Bases (E2 Zaitsev Product)
- Alkyl Halide Reactions: Gabriel Synthesis (Potassium Phthalimide → Primary Amine)
- Alkyl Halide Reactions: Ester Formation using Carboxylate Ions
- Alkyl Halide Reactions: SN2 Substitution Reactions
- Alkyl Halide Reactions: Generic SN2 (NaOCH3 / NaOEt / NaOH / NaSH / NaSR)
- Alkyl Halide Reactions: Generic SN1 Solvolysis
- Alkyl Halide Reactions: E1 Elimination via Hot Solvolysis
- Alkyl Halide Reactions: Monosodium Acetylide Alkynylation
- Alkyl Halide Reactions: Grignard Formation with Magnesium (RMgX)
- Corey–House (Gilman) Coupling — R₂CuLi with Alkyl Halides
- Alkyl Halide Reactions: Dihalide → Alkyne using excess NaNH₂, then H₂O