Abstract
This article depicts the reactivity study of olefins towards nucleophilic and electrophilic reactions. The real-time NMR kinetic experiments showcased how the reactivity of the olefins varies with varying electron density over the olefinic bond. Additionally, the SC-XRD study reveals not only the electron density over olefin makes the difference in reactivity but the planar arrangement also has an impact and could nullify these substitution effects.