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Question- Imagine a meta-xylene with -NO2 and -NH2 groups attached as substiuents to its benzene ring (in place of an H atom for each group). If the -NO2 group is directly between the meta-xylene methyl groups and the -NH2 group is para to the -NO2 group, significantly different B/L basicity is observed for the -NH2 group than if the -NH2 grup is directly between the meta-xylene methyl groups and the -NO2 group is para to the -NH2 group. Explain with lewis structure analysis and resonace effects. Note: consider steric effects
Separate your answers with a comma. Show the process and each step.
Show all the steps in the mechanism for the following reaction, When benzene is mixed with deuterated sulfuric acid, deuterium is slowly incorporated onto the ring. Show the mechanism for this reaction and explain how this relates the sulfonation of ..
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