Indicate the missing products of the reaction. When filling in the product indicate only the major organic product(s). There may be more than one acceptable answer. If you believe no reaction would occur, write NR. Denote stereochemistry where appropriate.

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Q4: A reaction forms the ortho, meta, and
Q5: Which of these statements is not true
Q6: Which compound reacts slowest during nitration?
Q7: Which of these is a meta-directing group
Q8: Which compound would be the most reactive
Q10: Provide detailed, arrow-pushing mechanisms for the transformation.
Q11: The -NH2 group is an ortho/para-director. So,
Q12: Indicate whether the compound should undergo nitration
Q13: Indicate whether the compound should undergo nitration
Q14: Devise a two-step synthesis to form
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