Reactivity of C=C C—C Electrons in pi bond are loosely held Electrophiles are attracted to the pi electrons. · Carbocation intermediate forms. Nucleophile adds to the carbocation. · Net result is addition to the double bond
Tautomerism in C=O and C=NR Systems C=O Enolization with Metal Amide Bases C=O Enolization: Kinetic Acidities Mild Methods for Enolate Generation Enolate Structure: A Survey of X-ray Structures