Chapter 20: Q60 (page 812)
Propose at least three methods to convert
Short Answer
Method 1
Method 2
Method 3
Chapter 20: Q60 (page 812)
Propose at least three methods to convert
Method 1
Method 2
Method 3
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Get started for freeDraw the products formed when A or B is treated with each reagent. In some cases,no reaction occurs.
Explain why the carbon of an ,-unsaturated carbonyl compound absorbs farther downfield in the NMR spectrum than the a carbon, even though the carbon is closer to the electron-withdrawing carbonyl group. For example, the carbon of mesityl oxide absorbs at 150.5 ppm, while the carbon absorbs at 122.5 ppm.
Treatment of compound C (molecular formula ) with , followed by H2O, affords compound D (molecular formula ). Compound D has a strong peak in its IR spectrum at 3600โ3200 . The NMR spectral data of C and D are given. What are the structures of C and D?Compound C signals at 1.3 (singlet, 6 H) and 2.4 (singlet, 2 H) ppm Compound D signals at 1.2 (singlet, 6 H), 1.6 (singlet, 1 H), 2.7 (singlet, 2 H), and 7.2 (multiplet, 5 H) ppm
Devise a synthesis of the given alcohol from benzene, organic alcohols having four or fewer carbons, and any needed inorganic reagents.
Draw the product formed when the -unsaturated ketone A is treated with each reagent.
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