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 8.1a
12020-08-28T07:27:02-07:00Julio Terra2fb22914f73f9e5a767bf7fb83987dca0e153e4a359922plain2020-08-28T07:27:19-07:00Julio Terra2fb22914f73f9e5a767bf7fb83987dca0e153e4aThe first and third structures are the same. The second and fourth and fifth structures are the same.
a. Convert the following Newman projections into bond-line drawings and indicate if any are duplicates (i.e. the same structure). SOLUTION
b. Convert the following bond-line drawings into Newman projections along the C2-C3 bond. Rotate your resulting projection to the lowest energy conformation. SOLUTION
If you made some mistakes or want to practice more, review the concepts that gave you trouble and work on this extra problem. If you're good, move to the problem below ;)
Problem 8.2: Fischer Projections
Label each of the following pairs of structures as enantiomers, diastereomers, or representations of the same compound (identical): SOLUTION
Convert the following bond-line drawings into Fischer projections with C1 at the top. SOLUTION
If you made some mistakes or want to practice more, review the concepts that gave you trouble and work on this extra problem. If you're good, move to the next lecture ;)
