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- Treatment of 2-methylpropanenitrile [(CH3)2CHCN] withCH3CH2CH2MgBr, followed by aqueous acid, affords compound V, whichhas molecular formula C7H14O. V has a strong absorption in its IRspectrum at 1713 cm−1, and gives the following 1H NMR data: 0.91(triplet, 3 H), 1.09 (doublet, 6 H), 1.6 (multiplet, 2 H), 2.43 (triplet, 2 H), and2.60 (septet, 1 H) ppm. What is the structure of V?Distinguish between them through H-NMR ? Fe Fe 3Chemistry what is it the reang of 1HNMR and 13C NMR spectra for this compound?
- Shown below are carbon NMR spectra for various isomers of C5H11Br. Assign structures for the compound that would produce each spectrum.Analyze the 1H AND 13C NMR spectrum of C8H9NO given below and draw the structure of the compound.Predict the masses and the structures of the most abundant fragments observed in the mass spectra of the followingcompounds. cyclohexyl isopropyl ether [cyclohexyl¬O¬CH(CH3)2]
- Choose the data that best matches this partial structure; the hydrogens represented by the data are in bold: H H H Od, 2H, 4.0 ppm Os, 2H, 7.1 ppm Od, 2H, 6.8 ppm Ot, 2H, 6.9 ppm HFollowing is a 1H-NMR spectrum of 2-butanol. Explain why the CH2 protons appear as a complex multiplet rather than as a simple quintet.3-Chlorocyclopropene, on treatment with AgBF4, gives a precipitate of AgCl and a stable solution of a product that shows a single 1H NMR absorption at 11.04 δ. What is a likely structure for the products, and what is its relation to HĂ¼ckel’s rule?