Chapter 20: Q81 (page 816)
Draw a stepwise mechanism for the following reaction of a Grignard reagent with a cyclic amide.
Chapter 20: Q81 (page 816)
Draw a stepwise mechanism for the following reaction of a Grignard reagent with a cyclic amide.
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Devise a synthesis of (E)-tetradec-11-enal, a sex pheromone of the spruce budworm, a pest that destroys fir and spruce forests, from acetylene, , and any needed organic compounds or inorganic reagents
Draw a stepwise mechanism for the following reaction.
Treatment of compound E (molecular formula ) with excess yieldscompound F (molecular formula ) after protonation with . E shows a strongabsorption in its IR spectrum at 1743. F shows a strong IR absorption at 3600โ3200.The NMR spectral data of E and F are given.
What are the structures of E and F?
Compound E signals at 1.2 (triplet, 3 H), 2.0 (singlet, 3 H), and 4.1 (quartet, 2 H) ppm
Compound F signals at 0.9 (triplet, 6 H), 1.1 (singlet, 3 H), 1.5 (quartet, 4 H), and 1.55(singlet, 1 H) ppm
Synthesize each compound from cyclohexanol using any other organic or inorganic compounds.
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