Zoe Alexander
Organic Chemistry teacher | Tutor for 8 years
I hold a degree in Organic Chemistry from Clemson University. With a passion for unlocking the mysteries of molecules, I bring expertise in the intricate world of organic compounds. Whether it's unraveling chemical reactions or demystifying complex structures, I thrive on helping students grasp the fundamentals of Organic Chemistry. My approachable style and commitment to student success make learning an enriching journey. Let's delve into the fascinating realm of molecules together and conquer any challenges along the way.
Questions
How can I draw 1,2,3,4,5,6-hexachlorocyclohexane with all the chloro groups in axial positions?
How do you perform a Williamson ether synthesis?
What does this reaction yield: #HC_2H_3O_2 + NaOH#?
Why do Grignard reactions need to be dry?
How can you determine whether a molecule is an enantiomer?
How could IR spectroscopy distinguish between #CH_3CH_2CH_2OH# and #CH_3CH_2OCH_3#?
The pure #beta# and #alpha# forms of D-glucose rotate the plane of polarized light to the right by 112° and 18.7° respectively (denoted as +112 and +18.7). Are these two forms of glucose enantiomers or diastereomers?
Why are epoxides important?
What is an organic compound found in most cells?
What are the steps to name aromatic hydrocarbons?
How can you distinguish between primary, secondary, and tertiary alcohols?
How many enantiomers does glucose have?
How would you draw all of the resonance structures for nitrate?
How is infrared spectroscopy used in forensic science?
How to prepare acetone from acid?
How would you convert an aldehyde to a ketone?
How do nuclei in the higher energy state return to the lower state?
What are the chiral centers in sucralose?
Why are alkyl iodides MORE reactive than alkyl fluorides?
How does pH relate to pKa?