Easton Jones
Organic Chemistry teacher | Experienced educator in USA
I hold a degree in Organic Chemistry from Pennsylvania College of Technology. With a passion for unraveling the complexities of organic compounds, I offer expertise in guiding students through the intricacies of this field. My approach emphasizes clarity, practical applications, and fostering a deep understanding of chemical principles. From fundamental concepts to advanced topics, I strive to empower students to excel in their academic endeavors. Let's embark on a journey of discovery and mastery together.
Questions
Why is infrared spectroscopy used in organic chemistry?
How does electronegativity change from top to bottom?
How do you name alkenes and alkynes?
How do you name cycloalkanes with double bonds?
How is the total number of electrons represented in a Lewis structure determined?
What are the products when glycine, β-alanine, γ-aminobutyric acid are heated?
What is the structure of the molecule named phenylacetylene?
Why is the epoxidation of cholesterol stereoselective?
Which molecules are achiral and chiral?
How do London dispersion forces affect boiling point?
What bonding feature allows you to differentiate among an alkane, alkene, alkyne, and an aromatic?
What is the Lewis Dot Structure for Phosphorus trichloride?
Why do diabetics have the fruity smell of ketones on their breath?
How many enantiomers does glucose have?
What is the reason for these compounds to undergo Sn1 or Sn2 or both mechanisms?
Is the London dispersion force greater between molecules of hydrogen sulfide (H2S) or molecules of water (H2O)?
How would you draw the hydrogenation reaction 2-methyl-2-butene and name the product?
Why does the carbonyl oxygen get protonated instead of the ether oxygen in the acid-catalyzed hydrolysis of amyl acetate?
Is #H_2N# the amino functional group?
How can I draw the cis-1-bromo-3-methylcyclohexane chair conformation?