A compound with the formula C7H14O has strong IR signals near 2900 and 1720 cm –1. The 1H NMR spectrum is tabulated below. Provide an unambiuous structural formula for the compound from the data provided.
1.07 ppm (6H doublet)
2.77 ppm (1H septet)
Frequently Asked Questions
What scientific concept do you need to know in order to solve this problem?
Our tutors have indicated that to solve this problem you will need to apply the Structure Determination without Mass Spect concept. You can view video lessons to learn Structure Determination without Mass Spect. Or if you need more Structure Determination without Mass Spect practice, you can also practice Structure Determination without Mass Spect practice problems.
What is the difficulty of this problem?
Our tutors rated the difficulty ofA compound with the formula C7H14O has strong IR signals nea...as high difficulty.
How long does this problem take to solve?
Our expert Organic tutor, Chris took 7 minutes and 21 seconds to solve this problem. You can follow their steps in the video explanation above.
What professor is this problem relevant for?
Based on our data, we think this problem is relevant for Professor Miller's class at UNH.