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
Is it easy recognize a meso compound?
How would you draw an alkane that has more than 3 but less than 10 carbon atoms and only primary hydrogens?
How can I draw the following esters: ethyl butanoate, pentyl propanoate, propyl 3-ethylhexanoate?
Why are London dispersion forces related to boiling point?
What is the process that forms large organic molecules?
How do you number cycloalkanes?
How can you tell e and z isomers apart?
How many sigma and pi bonds are there in #C_2(CN)_4#?
What functional groups are present in salicylic acid?
What is the difference between a dipole and an induced-dipole?
How do acid-base reactions differ from oxidation-reduction (or redox) reactions?
Why is bromine an electrophile?
Do E1 reactions require a strong base, like E2 reactions?
What is difference between hydrogenation and hydrogenolysis?
What is the general formula of an alkane?
How can I convert the bond line view of L-idose to a Fischer projection?
What is anisotropy in nmr?
What are the general reactions of the heterocyclic compounds?
How can electronegativity be measured?
Why do we need anhydrous ether to form a grignard reagent?