Madison Anderson
Organic Chemistry teacher | Experienced educator in USA
I hold a degree in Organic Chemistry from Robert Morris University. My passion lies in unraveling the mysteries of chemical compounds and reactions. With a solid academic background and years of teaching experience, I specialize in simplifying complex concepts to foster deep understanding. Whether it's elucidating mechanisms or tackling synthesis problems, I'm dedicated to empowering students to excel in their studies. Let's embark on this journey of discovery together.
Questions
How do we determine #D# and #L# terms, and how do they relate to absolute configuration?
Why are halogens electrophiles?
How is infrared spectroscopy used?
Is acetone a protic or an aprotic polar solvent?
How can I draw for cis -1,2-diethylcyclohexane the two chair conformers and indicate which conformer is more stable?
Can cis and trans isomers exist for an alkane?
If a pure R isomer has a specific rotation of –142.0°, and a sample contains 77.0% of the R isomer and 23.0% of its enantiomer, what is the observed specific rotation of the mixture?
How many stereoisomers and chiral carbons are there on a 1,3,5-trimethyl cyclohexane molecule?
How did the Hooke’s law help IR in the position of absorption bands?
How do you start from benzene to synthesize this aldol condensation product?
Why is the homolytic cleavage of the breaking bond drawn with a 'fish-hook' arrow?
What are the structural isomers of C9H20?
Is benzene hexachloride is an aromatic compound ? How it is prepared ?
How many resonance structures are there for S2O2 and S2O3?
Please give the IUPAC name of benzyl ethyl ether?
How can alkenes be made from alkanes?
Will the major resonance structure always have fewer formal charges?
How does the mechanism for hydroborations with #R_2 BH# in alkene happen?
What is the nucleophile in Fischer Esterification?
How do dipole dipole forces arise?