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
Why do #SP^2# hybrid orbitals form?
Is boron trihydride (#"BH"_3#) a base?
How do alkenes react with bromine water?
Why are cycloalkanes used as fuels?
What shape is a molecule of methane? Symmetrical or asymmetrical?
How would you calculate the formal charge of CO2?
What are dipoles in chemistry?
What is the electrophilic aromatic substitution mechanism?
What is the bond angle in cumulene (C4H4), of the C=C=C bond and the H-C-H bonds?
How it is possible to rank radical stability?
Do halogens appear in the IR spectrum? For example, bromine attached to a benzene molecule, where would the bromine appear on the IR spectra?
What alkene would you start with if you wanted to synthesize ethylcyclopentane?
A molecular formula is #C_4H_8O_2#. It has a degree of unsaturation of 1. Also it has an #OH# group, #CH_3# (sp3) group, and #C=O# group. What functional groups can be present?
Can anyone help out in solving these 4 questions under Question 4?
Is 3,4-diethylhexane a meso compound?
How many chiral carbons does 2,4-dimethyl pentane have?
What functional groups are present in the antibiotic penicillin?
Why are alkynes less reactive than alkenes in electrophilic addition reactions?
What is the difference between constitutional isomers and stereoisomers?
Why is the borane–THF complex used for hydroboration?