### Analyzing the Multiplicity of a ¹H NMR Peak#### Instructions:Consider the multiplicity of the ¹H NMR peak shown below. Identify how many hydrogens are on the neighboring carbon(s).#### NMR Spectrum Overview:- **Graph Description**: The NMR spectrum displays a triplet, which indicates a peak with three distinct lines of nearly equal height. This suggests splitting due to hydrogen atoms on adjacent carbon atoms.#### Numerical Input Interface:- **Hydrogens Calculator**: - Number pad available with digits from 1 to 9. - Includes buttons for decimal point (`.`) and plus/minus (`+/-`). - This feature enables students to input the number of hydrogens on neighboring carbon atoms based on the observed multiplicity.#### Explanation:The presented triplet implies that there are two neighboring hydrogen atoms (n+1 rule of NMR spectroscopy, where n is the number of hydrogens on adjacent carbons). This is a typical splitting pattern observed in proton NMR spectroscopy when interacting hydrogens are present on adjacent carbons.

Multiplicity of a peak corresponding to a hydrogen in 1H NMR spectroscopy is used to determine how…

Answered: Consider the multiplicity of the 1¹H…

Consider the multiplicity of the 1¹H NMR peak shown below. Identify how many hydrogens are on the neighboring carbon(s). 1 4 7 +/- 2 5 8 . Hydrogens 3 6

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Concept explainers

NMR Spectroscopy

NMR stands for Nuclear Magnetic Resonance in which the study of different molecules is done based on the interaction of radiofrequency electromagnetic radiations with the nuclei of molecules placed in a strong magnetic field. A precise study of spectra of visible light and all bands of electromagnetic radiation is called spectroscopy.

Question

### Analyzing the Multiplicity of a ¹H NMR Peak

#### Instructions:
Consider the multiplicity of the ¹H NMR peak shown below. Identify how many hydrogens are on the neighboring carbon(s).

#### NMR Spectrum Overview:
- **Graph Description**: The NMR spectrum displays a triplet, which indicates a peak with three distinct lines of nearly equal height. This suggests splitting due to hydrogen atoms on adjacent carbon atoms.

#### Numerical Input Interface:
- **Hydrogens Calculator**:
- Number pad available with digits from 1 to 9.
- Includes buttons for decimal point (`.`) and plus/minus (`+/-`).
- This feature enables students to input the number of hydrogens on neighboring carbon atoms based on the observed multiplicity.

#### Explanation:
The presented triplet implies that there are two neighboring hydrogen atoms (n+1 rule of NMR spectroscopy, where n is the number of hydrogens on adjacent carbons). This is a typical splitting pattern observed in proton NMR spectroscopy when interacting hydrogens are present on adjacent carbons.

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