The compound shown below is the cyclic hemiacetal of

Which of the following is the reactive intermediate in the nucleophilic substitution of 4-bromo-1-nitrobenzene with sodium hydroxide?

Identify the correct IUPAC name of the compound below.

Identify how you could synthesize an enamine.

Which of the following reactions would produce t-butylbenzene as the major product?

Bonus question Provide a stepwise synthesis for the following.      he answer should be entered as in the following example: (this is an example!) 1. NaNH2   2. CH3CH2Br   3. H2, Lindlar’s Cat.    4. BH3, THF   5. H2O2, NaOH                          (Keep five spaces between each step) All chemicals and reagents  structures should be correct and with the proper sequence. No partial credit.

Which of the following substituents is a moderate activator and an o/p director in electrophilic aromatic substitution reactions?

Provide the product for the following reaction sequence.

Which of the following is the first step in the general mechanism for electrophilic aromatic substitution reactions?

What is the product of the following sequence of reactions?