Concept explainers
(a)
Interpretation:
The structure of optically inactive compound A with the molecular formula
Concept introduction:
Many nuclei and electrons have spin. Due to this, a spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an
(b)
Interpretation:
The structure of isomer of compound A that has a different melting point and almost identical NMR spectra as that of A is to be stated.
Concept introduction:
Many nuclei and electrons have spin. Due to this, a spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.
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Organic Chemistry
- Determine the correct structure of the compound, which shows following 13C NMR DEPT-135 data is 13C NMR DEPT-135: negative peaks at δ30.2, 31.9, 61.8, 114.7 ppm; positive peak at 130.4 ppm.arrow_forwardWhen compound A (C5H12O) is treated with HBr, it forms compound B (C5H11Br). The 1 H NMR spectrum of compound A has a 1H singlet, a 3H doublet, a 6H doublet, and two 1H multiplets. The 1 H NMR spectrum of compound B has a 6H singlet, a 3H triplet, and a 2H quartet. Identify compounds A and B.arrow_forwardIdentify the structures of isomers A and B (molecular formula C8H9Br).arrow_forward
- Compounds A and B are isomers having the molecular formula C4H8O3. Identify A and B on the basis of their 1H NMR spectra.Compound A: δ 1.3 (3H, triplet); 3.6 (2H, quartet); 4.1 (2H, singlet); 11.1 (1H, broad singlet)Compound B: δ 2.6 (2H, triplet); 3.4 (3H, singlet); 3.7 (2H triplet); 11.3 (1H, broad singlet)arrow_forwardA compound has a formula of C19H16- Five signals appear in its 1°C NMR spectrum-one at 57 ppm and the remaining four between 126 and 144 ppm. In its 'H NMR spectrum, an unresolved multiplet (15 H) appears between 6.9 and 7.44 ppm and a singlet (1 H) appears at 5.5 ppm. What is the structure of this compound?arrow_forwardNonearrow_forward
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- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning