Ava Andrews
Organic Chemistry teacher | Experienced educator in USA
I'm an Organic Chemistry graduate from Montana State University Billings. With a passion for science and a knack for breaking down complex concepts, I'm here to help unravel the mysteries of chemistry. Whether it's understanding reaction mechanisms or tackling synthesis problems, I'm dedicated to guiding students toward mastery. Let's embark on this educational journey together, where every question is an opportunity to deepen our understanding of the molecular world.
Questions
How many sigma and pi bonds are in benzene?
How do you read IR spectra?
How does sulfuric acid catalyze the preparation of esters?
2-bromo-3-methylbutane , 2-chlorobutane , 1-chloro-2,2-dimethylpropane. Name the haloalkanes which can be prepared in high yield by monohalogenation of an alkane?
How are molecular orbitals determined?
How can I draw 1,2,3,4,5,6-hexachlorocyclohexane with all the chloro groups in axial positions?
How are functional groups important?
What is the difference between the physical properties of enantiomers and diastereomers?
Which molecules are achiral and chiral?
What is an ambident nucleophile?
How do geometric isomers occur?
What is the expected outcome from the electrophilic substitution of chlorobenzene with HNO3/H2SO4 and heat?
What is allylic halogenation?
How many valence electrons are used to make sigma and pi bonds in the #C_3H_6# molecule? How many valence electrons remain in nonbonding pairs in the molecule?
Could someone please explain (ii)* to me?
What is the mechanism for the hydroxymercuration-demercuration of n-butyne?
Can diastereomers be separated?
How can I convert d-talose bond line view to Fischer projection?
Is this numbering on the organic compound which has both alkene and alkyne is correct?
How do you prioritize the groups on chiral centers?