A compound A of molecular formula C4H8 shows 3 signals in its proton decoupled l3C NMR...

Question

Question

A compound A of molecular formula C4H8 shows 3 signals in its proton decoupled l3C NMR

spectrum and 2 signals in its IH NMR spectrum. Draw a plausible structure for compound A

Please explain very clearly thank you!!

science chemistry

Answer 1

Answer #1

Answer 2

Similar Homework Help Questions

Propose a reasonable structure based on the molecular formula, the 1H NMR, and the proton–decoupled 13C...

Propose a reasonable structure based on the molecular formula, the 1H NMR, and the proton–decoupled 13C NMR data below. The unknown compound has a molecular formula of C7H16O and * = CH2 by DEPT. Propose a reasonable structure based on the molecular formula, the 'H NMR, and the proton-decoupled 13C NMR data below. The unknown compound has a molecular formula of C7H160 and * = CH2 by DEPT. 'H NMR 3H 8H 13C NMR 2H (CH3)4 Si 26 VIH them...
Propose a reasonable structure based on the molecular formula, the 'H NMR, and the proton-decoupled *C...

Propose a reasonable structure based on the molecular formula, the 'H NMR, and the proton-decoupled *C NMR data below. The unknown compound has a molecular formula of C7H160 and * = CH2 by DEPT. 'H NMR 3H 8H HC NMR 2H (CH3), Si 3.5 0.0 40 3.0 2.5 2.0 1.5 1.0 0.5 300-MHZ 'H NMR spectrum ppm (8) "C NMR spectrum ppm (5)
Propose a reasonable structure based on the molecular formula, the^1H NMR, and the proton-decoupled^13C NMR data...

Propose a reasonable structure based on the molecular formula, the^1H NMR, and the proton-decoupled^13C NMR data below. The unknown compound has a molecular formula of C_7H_16O_2.

Compound B (C8H12O2) shows a strong carbonyl absorption in its IR spectrum. The broadband proton-decoupled 13C...

Compound B (C8H12O2) shows a strong carbonyl absorption in its IR spectrum. The broadband proton-decoupled 13C NMR spectrum of B has only three signals, at δ 19 (CH3), 71 (C), and 216 (C). Propose a structure for B.
2. (10 points) The proton NMR spectrum of a compound with a formula CsH100 is shown....

2. (10 points) The proton NMR spectrum of a compound with a formula CsH100 is shown. The decoupled carbon-13 and DEPT results are show in the table. The infrared spectrum shows a broad peak at about 3340cm and a medium peak about 1650 cm. Draw a structure for this compound and explain the data. Decoupled "CNMR, DEPT- DEPT-90 ppm 135 22.2 positive no peak 40.9 negative no peak 60.2 negative no peak 112.5 negative no peak 142.3 no peak no...
Draw the structure that corresponds to the following information: Molecular formula: C4H8O Proton-decoupled 13C NMR: (delta)...

Draw the structure that corresponds to the following information: Molecular formula: C4H8O Proton-decoupled 13C NMR: (delta) 26.5, (delta) 68.4.

3. From the NMR spectrum below, determine the structure of the compound. The molecular formula is...

3. From the NMR spectrum below, determine the structure of the compound. The molecular formula is C4H7BrO2 . There are no 1H NMR signals outside of the region shown. 3. (5 points) From the NMR spectrum below, determine the structure of the compound. The molecular formula is C4H-BrO2. There are no 'H NMR signals outside of the region shown.
Draw the structure that corresponds to the following molecular formula and proton decoupled 13C NMR-DEPT spectral...

Draw the structure that corresponds to the following molecular formula and proton decoupled 13C NMR-DEPT spectral data set (attached protons in parentheses): Molecular Formula: C4H6O Spectral data: ? 27.2 (3H), ? 127.8 (2H), ? 136.4 (1H), ? 197.7 (zero H).
The broadband proton-decoupled 13C NMR spectrum of a hexyl chloride exhibits six signals. Which of these...

The broadband proton-decoupled 13C NMR spectrum of a hexyl chloride exhibits six signals. Which of these structures could be the correct one for the compound? The broadband proton-decoupled 13c NMR spectrum of a hexyl chloride exhibits six signals. Which of these structures could be the correct one for the compound? Note diastereotopic groups are possible CH3 CH3CCH2CH2CI CH3 CH3 CHACHCHCH2CH3 CH3 CH3CCHCH3 CI CH3CH2CCH20% CH3 O CH3 CH3 CH3C-CHCH3

Draw the structure of a compound of molecular formula C4H8O that has a signal in its...

Draw the structure of a compound of molecular formula C4H8O that has a signal in its 13C NMR spectrum at >= 160 ppm. Then draw the structure of an isomer with no rings of molecular formula C4H8O that has all of its NMR signals at ^13C NMR signals at < 160 ppm. Structure that has a signal >= 160 ppm: draw structure Structure with no rings that has all signals < 160 ppm: draw structure