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 E10.1b
12020-03-01T15:34:35-08:00Julio Terra2fb22914f73f9e5a767bf7fb83987dca0e153e4a359921plain2020-03-01T15:34:37-08:00Julio Terra2fb22914f73f9e5a767bf7fb83987dca0e153e4aStrongest IMF in each set:
CH3CH2CH2CH2F, CH3CH2CH2CH2Cl, CH3CH2CH2CH2Br
CH3CH2CHO, CH3CH2COOH, CH3CH2CONH2 (COOH can dissociate to make ions in protic solvents, but amide has more H-bond donors, so depends on the solvent)