


Nolan Allen
Organic Chemistry teacher | Verified Expert
With a focus on Organic Chemistry, my passion lies in unraveling the complexities of molecules and their reactions. A graduate of Fairfield University, I bring a depth of knowledge and a knack for simplifying intricate concepts. Whether it's elucidating mechanisms or demystifying structures, I thrive on fostering understanding in my students. Let's embark on a journey through the fascinating world of organic chemistry together.
Questions
What is the common name of the solution of acetic acid and water?
How do you write out the mechanism for the reaction of #"C"_5"H"_11"OH"# with hot sulfuric acid to determine which option gives the greatest number of isomeric alkenes?
Is 3-methyloctane an alkane, alkene, or an alcohol?
What is adenosyl methionine tosylate disulfate?
Which of the following is not chiral: DCH2CH2CH2Cl, CH3CHDCH2Cl, CH3CHClCH2D, or CH3CH2CHDCl?
Can anyone help name these organic compounds and draw them out as well?
Why is the Lewis structure of ozone important?
What are examples of primary alcohols?
1bromopropane to 2bromopropane complete the reaction? Thanks
Which is more stable #cl-# or chlorine free redical ?
How do Grignard reagents react with alcohols?
When the aromatic hydrocarbon naphthalene reacts with nitric and sulfuric acids, two compounds containing one nitro group are formed. What are the structures of these two compounds?
Which alkenes will result in a meso-form when the alkenes below reacts with molecular bromide (#Br_2#) cold/dark?
Can H2O act as a lewis acid, lewis base, or both?
How can I interpret complicated NMR spectra?
If a pure R isomer has a specific rotation of –142.0°, and a sample contains 77.0% of the R isomer and 23.0% of its enantiomer, what is the observed specific rotation of the mixture?
How do you calculate the pH of a buffer solution?
How can halides be tested for?
Why do aromatic compounds give off a smoky flame?
What type of solvent favours SN1 mechanism?