CHEM1100 Study Guide - Final Guide: Tetrahedral Carbonyl Addition Compound, Hydrolysis, Iodine

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30 Jul 2018
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Bond breaking: homolytically: each atom of bond gets one electron; forms 2 radicals (odd electron species, half-headed arrow, heterolytically: atom of bond with higher electronegativity gets two electrons; forms 2 even electron species, full-headed arrow. Bond forming: homogenic: 2 radicals (odd electron species) donate one electron each to form a bond, heterogenic: two electrons donated from one species to another to form a bond. Electrostatic potential map: blue = electron poor (electrophile, red = electron rich (nucleophile) Reaction 1 - acid-base equilibria; the relative strengths of acids and bases. Electrophile (lewis acid: (cid:862)ele(cid:272)tro(cid:374) lo(cid:448)i(cid:374)g(cid:863, electron deficient, positive reaction site, positively polarized, electron-poor atom, can form a bond by accepting a pair of electrons from a nucleophile, specific to organic chemistry. Involve bond breaking and formation at carbon: acid-base reactions involve making bonds to hydrogen, direction of arrow is from nucleophile to electrophile, wherever there is four bonds around nitrogen it is a cation.

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