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Maya Allen
Organic Chemistry teacher | Tutor for 6 years
I hold a degree in Organic Chemistry from the University of Nebraska Medical Center. My passion lies in unraveling the mysteries of molecules and their reactions. With a strong foundation in both theory and practical application, I thrive on helping students navigate the complexities of organic chemistry. Through personalized guidance and clear explanations, I aim to demystify challenging concepts and foster a deeper understanding of the subject. Whether you're grappling with mechanisms or synthesis, I'm here to support you on your journey to mastery. Let's embark on this academic adventure together!
Questions
What isomeric Lewis structure of #CN_2H_2# has no formally charged atoms?
What are the sigma and pi bonds in cumulene?
When is it better to draw Sawhorse projections in comparison with other projections?
How do acid base reactions differ from redox reactions?
How do we draw #cis-1-"chloro"-"2"-"pentene"#?
What are epoxides used for?
Are there any methods to help with memorizing the formulas of organic functional groups (ex. alcohol, aldehyde, ketone, carboxylic acid, ester, amine, & amide)?
Why must the crude alkyl halide product be dried carefully with anhydrous #CaCl_2# before distillation?
How can I read in the NMR spectrum when increasing chemical shift?
Why are acetyl chloride or acetic anhydride used instead of acetic acid in preparing esters of acetic acid?
How does organic chemistry differ from inorganic chemistry?
How are alkyl halides reduced?
Which type of spectroscopy is more powerful?
What is the product of adding an amine (#RNH_2#) to #HCl#? What about #ArOH+NaHCO_3+NaOH#?
How many resonance structures does the O3 molecule have?
How do optical isomers compare physically and chemically?
Amines are organic compounds that contain what?
How do you depict chirality in molecules?
How many sigma bonds are in benzene?
How would you make a ketone from the aldehyde: cyclohexanecarbaldehyde?