Ellie Adams
Organic Chemistry teacher | Experienced educator in USA
I hold a degree in Organic Chemistry from Columbia College. My passion lies in unraveling the intricacies of molecular structures and chemical reactions. With a solid academic background and hands-on laboratory experience, I thrive on elucidating complex concepts in organic chemistry. As your tutor, I am dedicated to fostering a deep understanding and appreciation for the subject. Through personalized instruction and engaging discussions, I aim to empower students to excel in their studies and pursue their scientific aspirations. Let's embark on a journey of discovery and mastery together.
Questions
What are the functional groups in vitamin C?
PI3Br2 is a nonpolar molecule, how would you determine the bond angle of I-P-I bond , Br-P-Br bond and I-P-Br bond angles?
How do we compare the acidities of #Et_3SiOH# and #"methanol"#?
What are diatomic molecule examples?
What chemical starts off the chain reaction in the initiation step of an anti-markovnikov radical addition?
What is the #pi# -bond effect?
Why is a Grignard reagent a strong base?
How does pKa change with pH?
How does organic chemistry relate to nursing?
Which is a better electrophile: aldehydes, ketones, or carboxylic acids?
Which alkanes are solid at room temperature?
What are alkenes and alkynes used for?
What are the reactions for amines and amides?
How can I convert 3S,4R-dibromoheptane to a Fisher projection?
Do dipole-dipole interactions influence the evaporation of liquids and condensation of gases?
Why is an alkyl group is denoted by #"R"#?
Which diastereomer of 1-bromo-4-t-butylcyclohexane, the cis or the trans, undergoes elimination more rapidly when treated with sodium ethoxide?
Why is secondary carbocation more stable?
Why does #HCl#l have dipole dipole forces of attraction?
Which elimination reactions, E1 or E2, depend on the concentration of the substrate?