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TYPICAL QUESTIONS
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Why does one molecule end up with a monster name while another has a short one?
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How do I remember which bond stretches show up around 1700 cm⁻¹ versus 3300 cm⁻¹?
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1,3-butadiene + HBr → 3-bromo-1-butene (1,2-addition) vs. 1-bromo-2-butene (1,4-addition). Which dominates?
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Why is (CH₃)₃C⁺ more stable than CH₃CH₂⁺?
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I forget why the hydrogen adds to the carbon with more hydrogens already.
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Why does nitrobenzene (C₆H₅NO₂) send a new group to the meta position instead of ortho/para?
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