Ella Allen
Organic Chemistry teacher | Verified Expert
I hold a graduate degree in Organic Chemistry from Stetson University. With a passion for unraveling the intricacies of molecules, I thrive on simplifying complex concepts in chemistry. My journey in academia has equipped me to tackle diverse questions across subjects. Whether it's elucidating molecular structures or demystifying chemical reactions, I'm here to guide you. Let's navigate the world of science together, unraveling its wonders one question at a time. Join me in exploring the fascinating realms of knowledge, where every query sparks a new discovery.
Questions
How do you form #"ROMgI"# from #"RMgI"# reacting with ketones?
What is chloride's charge?
Why is aldehyde hydrogen not acidic?
Why is benzene resistant to addition reactions?
What is the difference between tautomerization and resonance?
How can the formation of sigma and pi bonds be explained?
A compound with 3 chiral centers will have how many stereoisomers?
Why is H2O a polar bond?
How do you draw cycloalkanes?
How are aldehydes and ketones alike?
Are alkyl groups polar or non-polar?
Why do we add #"HCl"# in a Grignard reaction workup?
What is an example of a ketone?
Is phenol more acidic than menthol?
How is ammonia represented by an electron dot diagram?
What is alkyl chloride?
Why is diethyl ether used to extract an organic product from water at the end of a reaction?
All possible stereoisomers for 3,3-dimethylpentane and 2-bromo-4-methylpentane?
Which of the following solvents are appropriate for NMR spectroscopy? Why?
Why does methanol (an alcohol) make methyl orange (an indicator) turn yellow?