Maya Allen
Organic Chemistry teacher | Tutor for 6 years
I hold a degree in Organic Chemistry from the University of Nebraska Medical Center. My passion lies in unraveling the mysteries of molecules and their reactions. With a strong foundation in both theory and practical application, I thrive on helping students navigate the complexities of organic chemistry. Through personalized guidance and clear explanations, I aim to demystify challenging concepts and foster a deeper understanding of the subject. Whether you're grappling with mechanisms or synthesis, I'm here to support you on your journey to mastery. Let's embark on this academic adventure together!
Questions
How can I draw the structures of the two enantiomers of alanine?
Which is more stable, cis -1-ethyl-2-methylcyclohexane or trans -1-ethyl-2-methylcyclohexane?
Do E2 reactions change stereochemistry?
How do the stereoisomers of 2-bromo-3-hexene arise?
What would be the major product obtained from hydroboration–oxidation in 2-methyl-2-butene?
How do polar protic solvents stabilize the chloride and bromide ions?
How are alkyl groups electron donating?
If the enantiomeric excess of a mixture is 79%, what are the percent compositions of the major and minor enantiomer?
How does an electron dot structure represent a covalent bond?
How does an SN2 reaction affect stereochemistry?
How can you account for energy of different conformers of ethane?
If an atom has sp3d hybridization in a molecule. What is the maximum number of pi bonds that atom can form?
How can you learn organic chemistry nomenclature?
What will the hydrolysis of an amide in HCl will produce?
Why are some epoxides toxic?
Based on Saytzeff's rule, select the most stable alkene: 1-methylcyclohexene, 3-methylcyclohexene or 4-methylcyclohexene?
How do you find the pH?
What is the functional group of an aldehyde?
Why is osmium tetroxide very expensive and highly toxic?
How can cis and trans isomers be separated?