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 many stereoisomers of a heptulose are possible? How many are D and how many are L sugars? How many names will be needed for all the isomers?
What is the representation of #"4-methylpent-2-yne"#?
How does electronegativity affect the polarity of the bond between two atoms?
How can I convert the bond line view of L-idose to a Fischer projection?
What are the function groups of aspirin?
How do you determine sp sp2 and sp3 orbitals?
How do you calculate the formal charge of #Cl# in #ClO^-# and #ClO_3^-#?
How did Lewis create his acids and bases model?
Are nonpolar covalent bonds uncommon?
What are the theory, conditions, and examples of electrophilic aromatic substitution?
What product will we get from the reaction (i) C6H5CHO + CH3CH2OH (reagent HCl)→ (ii) CH3CH2C(Cl)2CHO + H20 (reagent H+) → ?
Why do haloalkanes undergo nucleophilic substitution?
What is the major difference between a cyclic hemiacetal and a cyclic acetal?
How does one nucleus affect other nuclei in NMR?
What is the condensed structural formula for 2, 2-dimethylbutane?
What are structural isomers? Give me an example
What is adenosyl methionine tosylate disulfate?
How can I calculate formal charge?
How does an NMR spectrometer work?
When is Markovnikov’s rule valid?