CHEM 140A Chapter 2: Textbook Notes

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2. 2 ke(cid:455)s to u(cid:272)(cid:272)ess: usi(cid:374)g cu(cid:396)(cid:448)ed (cid:862)ele(cid:272)t(cid:396)o(cid:374)-pushi(cid:374)g(cid:863) a(cid:396)(cid:396)o(cid:449)s to des(cid:272)(cid:396)i(cid:271)e che(cid:373)i(cid:272)al rea(cid:272)tio(cid:374)s. Dissociation of polar covalent bond: general case: electrons move to more electronegative atom, arrow starts at bond and points toward the electronegative atom. Reactions involving double/triple bonds: additions: general case: an atom with a lone pair adds to the partial positive atom of a polarized multiple bond. Acid is proton donor, base is proton acceptor (bronsted lowry) Acid and base strengths measured by equilibrium constants: kw = 10-14 m2. Electrophiles and nucleophiles are similar to acids and bases: all nucleophiles are lewis bases. Contains at least one unshared pair of electrons: all electrophiles are lewis acids, nucleophilic substitution: substitution of a nucleophile for another atom or group in the starting organic molecule. General reaction of haloalkanes (organic compounds possessing carbon-halogen bonds) Functional groups/functionalities: characteristic properties that control reactivity of the molecule as a whole: carbon frame provides structure, while functional groups impart reactivity.

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