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
What are examples of geometric isomers?
How many constitutional isomers are possible for C4H9Br?
What are the resonance structures for #SO_2#?
Why must grignard reactions be anhydrous?
Why is a noncarbocation intermediate necessary for an antimarkovnikov halogenation to happen?
What are possible sources of error in an esterification lab?
How does sodium chloride differ from sodium and chlorine?
What is the esterification reaction equation of benzyl alcohol and acetic acid?
What does single covalent bond mean?
How are sigma bonds counted?
Does Anti-Markovnikov behaviour extend only to additions to alkenes?
Which atoms does a hydroxyl functional group contain?
How can I draw the molecular formula for an unsaturated alkyl chloride #C_5H_9Cl# with optical activity and E, Z – isomerism?
What is the trend in electronegativity with increasing atomic number?
How can electronegativity be used to determine bond polarity?
How can I calculate equivalent hydrogens?
What is the principle of flame emission spectroscopy?
How many asymmetric centers and stereoisomers does 1-Bromo-2-methylcyclopentane have?
How would you explain the electrophilic aromatic substitution with a diagram of a reaction mechanism?
How would you define electronegativity and explain how it influences the formation of chemical bonds?