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

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
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**Understanding NMR Multiplicity**

Consider the multiplicity of the \( ^1\text{H} \) NMR peak shown below. 

**Objective:**  
Identify how many hydrogens are on the neighboring carbon(s).

**Diagram Explanation:**

The diagram displays a proton NMR peak divided into multiple smaller peaks. This particular peak is split into several distinct lines, suggesting a specific splitting pattern associated with neighboring hydrogen atoms. 

**Interactive Component:**

On the right side, there is a numerical keypad under the title "Hydrogens," with numbers 1-9, a decimal point, and a button for modifying values. This interactive element appears to allow the input of the number of hydrogens present on adjacent carbons, helping to apply the n+1 rule for NMR splitting.

To deduce the number of neighboring hydrogens, count the individual peaks in the multiplet, subtract one, and use this value to predict the adjacent hydrogen count based on splitting patterns.
Transcribed Image Text:**Understanding NMR Multiplicity** Consider the multiplicity of the \( ^1\text{H} \) NMR peak shown below. **Objective:** Identify how many hydrogens are on the neighboring carbon(s). **Diagram Explanation:** The diagram displays a proton NMR peak divided into multiple smaller peaks. This particular peak is split into several distinct lines, suggesting a specific splitting pattern associated with neighboring hydrogen atoms. **Interactive Component:** On the right side, there is a numerical keypad under the title "Hydrogens," with numbers 1-9, a decimal point, and a button for modifying values. This interactive element appears to allow the input of the number of hydrogens present on adjacent carbons, helping to apply the n+1 rule for NMR splitting. To deduce the number of neighboring hydrogens, count the individual peaks in the multiplet, subtract one, and use this value to predict the adjacent hydrogen count based on splitting patterns.
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