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

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