Provide the reagents necessary to carry out the following conversion. 

Which one of the following substituents will direct the incoming group to the meta position during electrophilic aromatic substitution?

What is the correct IUPAC name for the following compound?  

What is (are) the product(s) of the following reaction?   

Which of the following oxidants would work for the following reaction?

Which of the following is the kinetic rate equation for the addition-elimination mechanism of nucleophilic aromatic substitution?

Which structure is consistent with this 1H NMR spectrum?

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.

Why are strongly acidic conditions not used in the formation of enamines and imines?

Which of the following is the reactive intermediate formed in the electrophilic nitration of nitrobenzene with HNO3 and H2SO4?