Addison Armstrong
Organic Chemistry teacher | Experienced educator in USA
Greetings! I am an Organic Chemistry specialist with a degree from Ferris State University. My passion lies in simplifying complex concepts and fostering a love for chemistry. With a commitment to student success, I leverage my academic background to provide clear and insightful explanations. Let's embark on a learning journey together, where every question is an opportunity for growth.
Questions
How to prepare pentabromobenzene from aniline?
Are SN1 reactions faster than SN2?
What are the steps to name aromatic hydrocarbons?
How do you classify Bronsted acids and bases?
What are the possible resonance structures of #CH_3-CH=CH-CH=O# and #CH_3-COO^-#? What is the order of stability of the contributing resonance structures?
What holds nonpolar covalent bonds together?
Why is SN2 stereospecific?
Why do non-polar solvents favour Sn2 reactions and why do polar solvents favour Sn1 reactions? Please simple ways. Thanks a lot
What are cycloalkanes used for?
Is the London dispersion force greater between molecules of hydrogen sulfide (H2S) or molecules of water (H2O)?
How do cis and trans isomers arise in cinnamaldehyde?
How do you draw a primary alcohol?
How can you isolate optical isomers?
How can I draw the structures of 4 isomers of amides for the formula #C_5H_11NO# ?
Is there a requirement for the stereochemistry of the starting material in E1 reactions? Why?
Why are imines brightly colored?
Is #H_2N# the amino functional group?
How does pKa affect equilibrium?
How do you determine pi bonds?
How are synthetic alkynes used for birth control?