Identify products A and B from the given 1H NMR data.
a. Treatment of CH2==CHCOCH3 with one equivalent of HCl forms compound A.A exhibits the following absorptions in its 1H NMR spectrum: 2.2 (singlet, 3 H), 3.05 (triplet, 2 H), and 3.6 (triplet, 2 H) ppm. What is the structure of A?
b. Treatment of acetone [(CH3)2C==O] with dilute aqueous base forms B. Compound B exhibits four singlets in its 1H NMR spectrum at 1.3 (6 H), 2.2 (3 H), 2.5 (2 H), and 3.8 (1 H) ppm. What is the structure of B?
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