Question: Ia. Compound A is more reactive than compound B in an electrophilic aromatic substitution at ortho position. Using resonance structures and text, explain this order

Ia. Compound A is more reactive than compound B in an

electrophilic aromatic substitution at ortho position. Using resonance structures and text, explain

Ia. Compound A is more reactive than compound B in an electrophilic aromatic substitution at ortho position. Using resonance structures and text, explain this order of reactivity. VIIIb. Compound C will favor nitration at the meta position over the ortho position. Explain why using resonance structures and text. HNO3/H2SO4 minor product

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