Madison Anderson
Organic Chemistry teacher | Experienced educator in USA
I hold a degree in Organic Chemistry from Robert Morris University. My passion lies in unraveling the mysteries of chemical compounds and reactions. With a solid academic background and years of teaching experience, I specialize in simplifying complex concepts to foster deep understanding. Whether it's elucidating mechanisms or tackling synthesis problems, I'm dedicated to empowering students to excel in their studies. Let's embark on this journey of discovery together.
Questions
How do Lewis acids and bases differ from Bronsted/Lowry acids and bases?
How do the structures of cyclohexane and benzene differ?
How are dipoles induced?
How can you distinguish between primary, secondary, and tertiary alcohols?
How does a spectrophotometer work?
Why does the rate of the E1 reaction depend only on the substrate?
How does the mass spectrometer work?
When do you use the Boltzmann Distribution in NMR?
Do enantiomers always change the color of light?
Is a Diels Alder reaction exothermic?
How it is aromatic ?
What is "breaking the Pi bond" in alkenes?
What is structure of the cis and trans isomers of the compound piperonal?
Is cyclohexane and isopropyl alcohol (2-propanal) miscible?
What do aromatic compounds contain?
How does bromine water show if something is an alkane or alkene?
Is #H_2N# the amino functional group?
How do you name #"H"_3"C"{"C"("CH"_3)_2}_2("CH"_2)_2"CH"_3# and #"H"_3"C""CH"_2("CH""CH"_2"CH"_3)("CH"_2)_2"CH"("CH"_3)_2#?
When should you use the #cis//trans# as opposed to #"(Z)-"//"(E)-"# isomer naming scheme and vice versa?
What is an example of an amino acid without a chiral carbon?