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 may I read NMR splitting?
How can I draw the following aldehydes and ketones: hexanal, heptan-3-one, 3-methyloctanal?
In reference to carbocations, what do we mean by stability? Are not all carbocations high energy species?
How does pKa relate to acidity?
What are sp2 hybrid orbitals?
How many carbon atoms would be in the simplest chiral alkane?
Why ethers only undergo cleavage with strong acids and not with weaker acids?
How do you count pi bonds?
Which is a more stable conjugated compound: the cis form or the trans form and why?
If both double bond and triple bond exist while naming a compound according to IUPAC system, to whom should i give importance first ?
What is the halogenation of alkenes?
What is the pKa of #CH_3COOH# and #H_3PO_4#?
What are the functional groups in lorazepam?
How do dipole-dipole forces cause molecules to be attracted to one another?
Which of the following is not an electrophile? How is this determined?
Why do aromatic rings absorb light?
How do you name unsymmetrical anhydrides?
Does #SF_4# have geometrical isomers?
What is an ambident nucleophile?
What is the Lewis Dot Diagram for #NF_3#?