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Organic ChemistryMain MenuLecture 1: Introduction to Molecular OrbitalsLecture 10: Intermolecular Forces and Intro to ReactivityLecture 11: Alkenes as Nucleophiles ILectures 12 and 13: Alkenes II & IIILecture 14: Benzenes as Nucleophiles ILecture 15 objectives and skillsLecture 2: Molecular Orbitals in Organic StructuresLecture 3: Molecular Orbitals and ResonanceLecture 4: Molecular Orbitals and AromaticityLecture 5: Nomenclature and IR SpectroscopyLecture 6: Stereochemistry ILecture 7: Stereochemistry IILecture 8: Newman and Fisher ProjectionsLecture 9: Conformations and Cyclohexane RingsJulio Terra2fb22914f73f9e5a767bf7fb83987dca0e153e4a
12020-04-11T13:38:45-07:00SOLUTION E21.1b1plain2020-04-11T13:38:45-07:00The second reaction is faster. The substrate is the same, but the leaving group is not. When alcohols are put in acidic solutions, the OH can be protonated to make a better leaving group (R-OH2+ vs R-OH). In both E1 and E2 reactions, the type of leaving group affects the activation energy. The first reaction is faster. The substrates, leaving group, and nucleophile are the same, but the solvent is different. Protic solvents better solubilize the carbocation and leaving group, improving both species’ stability. In E1 reactions, the stability of the carbocation affects the activation energy.
