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
SOLUTION E11.2b
12020-03-01T16:41:00-08:00Julio Terra2fb22914f73f9e5a767bf7fb83987dca0e153e4a359921plain2020-03-01T16:41:01-08:00Julio Terra2fb22914f73f9e5a767bf7fb83987dca0e153e4aThe major product (methyl ether) comes from the most stable carbocation intermediate adding the most abundant nucleophile (methanol, MeOH) rather than the chloride.
