Which of the Given Molecules Can Exhibit Tautomerism? An In-Depth Analysis
The straightforward solution is that molecules which possess labile (acidic) protons adjacent to a functional group capable of stabilizing a new double bond can exhibit tautomerism. In most common cases, this means that compounds featuring carbonyl groups (–CO–) with an adjacent CH or CH₂ group are likely candidates for keto-enol tautomerism. Other types, such as…