Provide detailed, arrow-pushing mechanisms for the transformation. Show all reactive intermediates. (It is not necessary to show every resonance structure for appropriate intermediates.)
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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
Q9: Indicate the missing products of the reaction.
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
Q15: Draw the major organic product for the
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