Provide an acceptable bond-line structure for 2,2,3,3,-tetramethylbutane
Provide an acceptable systematic IUPAC name for the following molecule
![](/old/images/nomen7.gif)
Provide an acceptable bond-line structure for Trans-1-isopropyl-2-methylcyclopropane
Provide an acceptable systematic IUPAC name for
![](/old/images/nomenclature-practice-problems.gif)
Provide an acceptable IUPAC name for
![](/old/images/organic-chemistry-naming.gif)
Provide an acceptable systematic IUPAC name for the following molecule
![](/old/images/nomenclature-quiz.gif)
Provide an acceptable bond-line structure for 4-ethyl-3,5-dimethylnonane
Provide an acceptable systematic IUPAC name for the following molecule
![](/old/images/nomenclature5.gif)
Provide an acceptable systematic IUPAC name for
![](/old/images/nomenclature6.gif)
Draw the resonance structure(s) for
![](/old/images/resonance2.gif)
Draw the resonance structure(s) for
![](/old/images/resonance3.gif)
For the following molecule, draw the resonance structure(s)
![](/old/images/resonance-structure1.gif)
Draw all possible resonance structures for the following molecule
![](/old/images/resonance6.gif)
Draw all possible resonance structures for the following molecule
![](/old/images/resonancestructure1.gif)
Draw the resonance structure(s) for
![](/old/images/resonancestructure2.gif)
Draw the resonance structure(s) for
![](/old/images/resonancestructure4.gif)
Draw the resonance structure(s) for
![](/old/images/resonancestructures7.gif)
Which proton is more acidic?
![](/old/images/acidbase.gif)
Rank the following molecules from weakest to strongest acid
A. CF3CH2OH
B.
![](/old/images/conjugate-acid.gif)
Draw the most stable chair conformation of methylcyclohexane