Give suitable structures for compounds A and B.
Compound A (C7H14O) burned with a yellow, nonsooty flame and did not decolorize a bromine–methylene chloride solution. It did give a positive 2,4-dinitrophenylhydrazine test, but a negative Tollens test. Treatment of the compound with lithium aluminum hydride followed by neutralization with acid, produced compound B, which gave a positive Lucas test in about 5 min. Compound B also gave a positive ceric nitrate test. The 1 H NMR spectrum for compound A gave the following data: 1.02 ppm 9H, singlet
2.11 ppm 3H, singlet
2.31 ppm 2H, singlet
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