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

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 reactions would produce t-butylbenzene as the major product?

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

Provide the product for the following reaction sequence.

What is the product of the following sequence of reactions?

Which of the following chlorobenzenes produces a single isomer upon treatment with NaNH2?

What would be the product of the following reaction?

Identify the preferred site(s) of electrophilic attack on the following compound.

Identify the products of the hydrolysis of the following compound.