Concept explainers
Interpretation:
The structure of compound of given molecular formula C7H12O2 to be predicted using 13CNMR spectra.
Concept introduction:
The 13CNMR spectrum gives information on the different electronic environments of carbon. As like 1HNMR, the number of signals generated in 13CNMR are predicted by performing symmetry operations (rotation or reflection symmetry). Only chemical shift values are reported in the spectrum but not the multiplicity and integration values because the coupling between two neighboring 13C-13 C nuclei are weakly involved due to the low abundance of 13C isotopes of carbon atom.
To Identify:
The structure of given molecular formula C7H12O2.
Broadband-decoupled 13CNMR spectrum:
The spectra provide information regarding the total number of carbon environments.
DEPT (Distortionless enhancement by polarization transfer):
a) DEPT-90: The spectrum exhibits signal only from CH group and no signals from CH3, CH2, CH and quaternary carbon (carbon with no protons).
b) DEPT-135: The spectrum exhibits CH3 groups and CH groups as positive signals (pointing up); CH2 groups appear as negative signals (pointing down) and quaternary carbon does not appear.
The signals appear in each type of spectrum:
Want to see the full answer?
Check out a sample textbook solutionChapter 13 Solutions
Bundle: Organic Chemistry, 9th, Loose-Leaf + OWLv2, 4 terms (24 months) Printed Access Card
- Bunsenite (NiO) crystallizes like common salt (NaCl), with a lattice parameter a = 4.177 Å. A sample of this mineral that has Schottky defects that are not supposed to decrease the volume of the material has a density of 6.67 g/cm3. What percentage of NiO molecules is missing? (Data: atomic weight of Ni: 58.7; atomic weight of O: 16).arrow_forwardA sample of aluminum (face-centered cubic - FCC) has a density of 2.695 mg/m3 and a lattice parameter of 4.04958 Å. Calculate the fraction of vacancies in the structure. (Atomic weight of aluminum: 26.981).arrow_forwardPlease correct answer and don't used hand raitingarrow_forward
- Please correct answer and don't used hand raitingarrow_forwardPlease correct answer and don't used hand raitingarrow_forwardWhich of the following species is a valid resonance structure of A? Use curved arrows to show how A is converted to any valid resonance structure. When a compound is not a valid resonance structurc of A, explain why not. Provide steps and tips on what to look for to understand how to solve and apply to other problems.arrow_forward
- N IZ Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. Molecule 1 Molecule 2 HN Molecule 3 Х HN www. Molecule 4 Molecule 5 Molecule 6 none of the above NH NH Garrow_forwardShow work with explanation. don't give Ai generated solutionarrow_forwardFollow the curved arrows to draw a second resonance structure for each species. Explain and steps for individual understanding.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning