Concept explainers
(a)
Interpretation:
Compounds from the
Concept introduction:
The
The splitting of signals predicts the number of hydrogens or protons attached to the adjacent carbon in a carbon chain of a compound. The single signal is split into multiple peaks called the multiplicity of the signal. Splitting of signals is done according to the
According to the
(b)
Interpretation:
Compounds from the
Concept introduction:
The
The splitting of signals predicts the number of hydrogens or protons attached to the adjacent carbon in a carbon chain of a compound. The single signal is split into multiple peaks called the multiplicity of the signal. Splitting of signals is done according to the
According to the
(c)
Interpretation:
Compounds from the
Concept introduction:
The
The splitting of signals predicts the number of hydrogens or protons attached to the adjacent carbon in a carbon chain of a compound. The single signal is split into multiple peaks called the multiplicity of the signal. Splitting of signals is done according to the
According to the
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Organic Chemistry
- Following are 1H-NMR spectra for compounds G, H, and I, each with the molecular formula C5H12O. Each is a liquid at room temperature, is slightly soluble in water, and reacts with sodium metal with the evolution of a gas. (a) Propose structural formulas of compounds G, H, and I. (b) Explain why there are four lines between 0.86 and 0.90 for compound G. (c) Explain why the 2H multiplets at 1.5 and 3.5 for compound H are so complex.arrow_forwardAscaridole is a natural product that has been used to treat intestinal worms. Explain why the two methyls on the isopropyl group in ascaridole appear in its 1H-NMR spectrum as four lines of equal intensity, with two sets of two each separated by 7 Hz.arrow_forwardWhat is the structure of an unknown compound with molecular formula C6H15N that gives the following 1H NMR absorptions: 0.9 (singlet, 1 H), 1.10 (triplet, 3 H), 1.15 (singlet, 9 H), and 2.6 (quartet, 2 H) ppm?arrow_forward
- 1) Propose the structures for the following 1H and 13C NMR spectrum. b) Molecular Formula: C8H8O3 1H-NMR, CDCl3 Solvent, Molecular Formula: C8H8O3 13C-NMR, CDCl3 Solvent, Molecular Formula: C8H8O3 in the picturesarrow_forwardHow many unique 13C NMR and 1H NMR signals exist in the spectrum for the compound: 1,3-dibromobenzene?arrow_forwardCompound X (molecular formula C10H120) was treated with NH2NH2, ¯OH to yield compound Y (molecular formula C10H14). Match the 1H NMR spectra of X and Y to the corresponding structures of X and Y. Compound NH2NH2 Compound 'H NMR of X 6 H OH Y 1 H 5H 8. 6. 4 ppm or H NMR of Y 6 H 2H 5H 1 H multiplet multiplet 8. 6. 4. 3. 1 nnm 2. 2. 3, O:arrow_forward
- Propose a structure consistent with each set of spectral data: a.C6H14O: IR peak at 3600−3200 cm−1; NMR (ppm): 0.8 (triplet, 6 H) 1.5 (quartet, 4 H) 1.0 (singlet, 3 H) 1.6 (singlet, 1 H) b.C6H14O: IR peak at 3000−2850 cm−1; NMR (ppm): 1.10 (doublet, relative area = 6) 3.60 (septet, relative area = 1)arrow_forward14. Compound B has molecular formula C9H12. It shows five signals in the 1H-NMR spectrum - a doublet of integral 6 at 1.22 ppm, a septet of integral 1 at 2.86 ppm, a singlet of integral 1 at 5.34 ppm, a doublet of integral 2 at 6.70 ppm, and a doublet of integral 2 at 7.03 ppm. The 13C-NMR spectrum of B shows six unique signals (23.9, 34.0, 115.7, 128.7, 148.9, and 157.4). Identify B and explain your reasoning.arrow_forward4. Deduce the structure of a compound with the molecular formular C8H10O that exhibits the following ¹H NMR and ¹³℃ NMR spectra. (6 pts) Proton NMR 22 7 Carbon NMR There are two. 160 unresolved lines at 130 ppm 140 120 5 Chemical Shift (ppm) 100 80 60 Chemical Shift (ppm) 40 3 20 2V 0arrow_forward
- Following are the 'H and 13C NMR spectra for each of three isomeric ketones with formula C7H14O. Determine a structure to each pair of spectra and assign each H and C. Carbon spectrum B Carbon spectrum C,H140 А C,H140 CDCI3 CDCI3 200 150 100 50 200 150 100 50 Proton spectrum C,H140 В Proton spectrum A C,H140 2.9 2.8 2.7 1.96 2.00 2.91 1.04 6.18 3.0 2.5 2.0 1.5 1.0 0.5 0.0 3.0 2.5 2.0 1.5 0.5 0.0 211.04 -44.79 –17.39 – 13.78 -218.40 -38.85 –18.55arrow_forwardHow many peaks would appear in 1H NMR and 13C NMR for the following structure (ignore splitting). 1H NMR: 13C NMR:arrow_forwardA compound has the molecular formula of C3HgO. It exhibits 4 peaks in its 1H NMR spectrum. These peaks are (in 8): 3.6 (2H, t). 2.3 (1H, broad), 1.6 (2H, sextet). 1.05 (3H. t). Which of the following compounds is consistent with this data? 0 0 OMe OH OH O H.C-O-CH. О OH Caarrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning