Question

Draw the structure of the compound C3H6Cl2 from its proton (1H) NMR spectrum below. First-order spin-spin...

Draw the structure of the compound C3H6Cl2 from its proton (1H) NMR spectrum below. First-order spin-spin splitting rules and equal coupling constants can be assumed. (Detailed analysis of any non-first order portions of the spectrum will not be required.) Integral ratios to the nearest whole number are (left to right) 1:2:3

Homework Answers

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
The proton NMR spectrum for a compound with the formula C7H12O2 is shown below along with...
The proton NMR spectrum for a compound with the formula C7H12O2 is shown below along with carbon-13 spectral data in tabular form. (It may be necessary to expand (zoom) some of the 1H signals to view spin-spin splitting details.) The infrared spectrum exhibits a strong band at 1743 cm-1 and a medium intensity band at 1236 cm-1. Draw a structure for this compound. Normal Carbon DEPT-135 DEPT-90 Proton Shift Relative Area 18.0 Positive No peak 1.71 3.1 21.0 Positive No...
The proton NMR spectrum for a compound with the formula C6H12O2 is shown below along with...
The proton NMR spectrum for a compound with the formula C6H12O2 is shown below along with carbon-13 spectral data in tabular form. (It may be necessary to expand (zoom) some of the 1H signals to view spin-spin splitting details.) This compound exhibits strong infrared absorption at 1738 and 1245 cm-1. 13C NMR Data Normal Carbon DEPT-135 DEPT-90 Proton Shift Relative Area 19.1 Positive No peak 0.93 6.0 20.9 Positive No peak 1.92 0.9 27.7 Positive Positive 2.06 3.0 70.6 Negative...
When reading a proton NMR spectrum, what information regarding molecular structure can be determined from: 1)...
When reading a proton NMR spectrum, what information regarding molecular structure can be determined from: 1) the chemical shift, 2) the area under each peak (the integration value), and 3) spin-spin splitting (the n + 1 rule)?
A compound, C14H12, shows IR peaks at 700, 740,and 890 cm-1. Its 1H NMR spectrum has...
A compound, C14H12, shows IR peaks at 700, 740,and 890 cm-1. Its 1H NMR spectrum has peaks at delta 7.3 (10 H, broad singlet) and 5.4 (2 H, singlet). Draw its structure in the window below.
A compound, C9H12, shows an IR peak at 750 cm-1. Its 1H NMR spectrum has peaks...
A compound, C9H12, shows an IR peak at 750 cm-1. Its 1H NMR spectrum has peaks at delta 7.1 (4 H, broad singlet), 2.6 (2 H, quartet, J=8 Hz), 2.3 (3 H, singlet), and 1.2 (3 H, triplet, J=8 Hz). Draw its structure in the window below.
A compound, C10H14, shows an IR peak at 745 cm-1. Its 1H NMR spectrum has peaks...
A compound, C10H14, shows an IR peak at 745 cm-1. Its 1H NMR spectrum has peaks at delta 7.18 (4 H, broad singlet), 2.70 (4 H, quartet, J=7 Hz), and 1.20 (6 H, triplet, J=7 Hz). Draw its structure in the window below. You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. In cases where there is more than one answer, just draw one.
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT