Chapter 14: Q14-65P (page 676)
The 1H NMR spectrum of 2-propane-1-ol is shown here. Indicate the protons in the molecule that are responsible for each of the signals in the spectrum.

Short Answer
.
/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none}
Learning Materials
Features
Discover
Chapter 14: Q14-65P (page 676)
The 1H NMR spectrum of 2-propane-1-ol is shown here. Indicate the protons in the molecule that are responsible for each of the signals in the spectrum.

.
All the tools & learning materials you need for study success - in one app.
Get started for free
How would integration distinguish the 1 H NMR spectra of the following compounds?

Describe the 1H NMR spectrum you would expect for each of the following compounds, indicating the relative positions of the signals:



Identify each of the following compounds from its molecular formula and its 13C NMR spectrum:
a.C4H10O

b.C6H12O

Identify the compound with molecular formula C7H14O that gives the following proton-coupled 13C NMR spectrum:

The 1 H NMR spectra of two carboxylic acids with molecular formula C3H5O2Cl are shown below. Identify the carboxylic acids. (The 鈥渙ffset鈥 notation means that the farthest-left signal has been moved to the right by the indicated amount to fit on the spectrum; thus, the signal at 9.8 ppm offset by 2.4 ppm has an actual chemical shift of 9.8 + 2.4 = 12.2 ppm.)

What do you think about this solution?
We value your feedback to improve our textbook solutions.