Provide an acceptable IUPAC name for the following molecule
![](/old/images/nomenclature.gif)
Provide an acceptable systematic IUPAC name for
![](/old/images/nomenclature2.gif)
Provide an acceptable systematic IUPAC name for the following molecule
![](/old/images/nomenclature3.gif)
Provide an acceptable systematic IUPAC name for
![](/old/images/nomenclature4.gif)
Provide an acceptable systematic IUPAC name for the following molecule
![](/old/images/nomenclature7.gif)
Provide an acceptable systematic IUPAC name for
![](/old/images/nomenclature8.gif)
Draw the resonance structure(s) for
![](/old/images/resonance.gif)
Draw the resonance structure(s) for
![](/old/images/resonance-structures.gif)
Draw all possible resonance structures for the following molecule
![](/old/images/resonance5.gif)
Draw the resonance structure(s) for
![](/old/images/resonancestructures2.gif)
Draw all possible resonance structures for the following molecule
![](/old/images/resonancestructures3.gif)
Draw the resonance structure(s) for
![](/old/images/resonancestructures4.gif)
Draw the resonance structure(s) for
![](/old/images/resonancestructures6.gif)
Draw all possible resonance structures for the following molecule
![](/old/images/resonancestructures8.gif)
Which hydrogen is more acidic?
![](/old/images/acidbase2.gif)
Draw the chair conformation of the cyclohexane molecule with all axial and equatorial positions shown
Assign priorities for the substituents attached to the stereocenter labeled red.
![](/old/images/stereochemistry.gif)
Is the stereocenter labeled red in the S or R configuration?
![](/old/images/stereochemistry-practice.gif)
Is the stereocenter in the S or R configuration?
![](/old/images/r-configuration.gif)
Draw a bond line drawing of S-3-bromohexane that actively shows the stereocenter.