Linked from

The 9 pages that link to Deprotonation, each with the reason it gives.

• Electrophilic aromatic substitutionRelated: A base removes the proton from the attacked carbon, restoring the ring's π system.

• BasicityRelated: Choosing a base for deprotonation depends on the relative acidities of the reactants and products.

• Friedel–Crafts acylationRelated: Loss of a ring proton restores aromaticity after carbon–carbon bond formation.

• Sodium hydrideRelated: Sodium hydride commonly converts weak acids into reactive anions by removing a proton.

• ZwitterionRelated: Deprotonation can leave a negatively charged group alongside a positive one.

• Sodium amideRelated: This is the central step when sodium amide generates carbon nucleophiles.

• Potassium hydrideRelated: Potassium hydride can remove acidic hydrogen atoms from organic compounds.

• E1cB elimination reactionRelated: It is the first step and creates the carbon-centered anion.