Questions from Organic Chemistry

Q: Starting with nitrobenzene and using any other reagents of your choice,

Starting with nitrobenzene and using any other reagents of your choice, outline a synthesis of para-chloroaniline.

Q: Identify all of the different β-hydroxyaldehydes that are formed when

Identify all of the different β-hydroxyaldehydes that are formed when a mixture of benzaldehyde and hexanal is treated with aqueous sodium hydroxide.

Q: Using acetic acid as your only source of carbon atoms, show

Using acetic acid as your only source of carbon atoms, show how you could make N-ethyl acetamide.

Q: Draw the major product that is expected when each of the following

Draw the major product that is expected when each of the following compounds is treated with excess methyl iodide followed by aqueous silver oxide and heat: a. Cyclohexylamine b. (R)-3-Methyl-2-buta...

Q: Phencyclidine (PCP) was originally developed as an anesthetic for animals

Phencyclidine (PCP) was originally developed as an anesthetic for animals, but it has since become an illegal street drug because it is a powerful hallucinogen. Treatment of PCP with excess methyl iod...

Q: Predict the major product obtained when each of the following amines is

Predict the major product obtained when each of the following amines is treated with a mixture of NaNO2 and HCl:

Q: Propose an efficient synthesis for each of the following transformations:

Propose an efficient synthesis for each of the following transformations:

Q: Identify the reactants you would use to prepare each of the following

Identify the reactants you would use to prepare each of the following azo dyes via an azo coupling reaction:

Q: As part of the effort to create new anti-cancer drugs

As part of the effort to create new anti-cancer drugs that selectively target cancer cells, scientists are developing light-activated compounds such as trans-PST-1, which can be prepared from compound...

Q: Pyridine undergoes electrophilic aromatic substitution at the C3 position. Justify this

Pyridine undergoes electrophilic aromatic substitution at the C3 position. Justify this regiochemical outcome by drawing resonance structures of the intermediate produced from attack at C2, at C3, and...