### Constructing a Simulated ¹H NMR Spectrum for 2-Chloropropane**Objective:** Create a simulated ¹H NMR spectrum for 2-chloropropane by assigning appropriate splitting patterns and integration values to the chemical shift baseline.**Instructions:**- Drag and drop the correct splitting patterns into the boxes on the chemical shift baseline.- Add integration values above each signal.- Splitting patterns and integrations may be reused as necessary.- Note: Peak heights do not indicate integration values.**Molecule:**- The structure depicted is 2-chloropropane.**Chemical Shift Baseline:**- The x-axis is labeled with values from 7 ppm to 0 ppm.**Answer Bank:**- Options for splitting patterns and integration values: - 1H - 4H - 5H - 6H - 2H - 3H**Graph Explanation:**- Two main boxes are indicated along the chemical shift baseline.- These boxes represent areas where you should place the splitting patterns from the answer bank.**Integration and Splitting Patterns:**- Match the splitting patterns and integration values to correctly simulate the NMR spectrum for 2-chloropropane. Consider the chemical environment and symmetry of hydrogen atoms in the molecule to determine the appropriate selections.This exercise helps illustrate the principles of NMR spectroscopy, focusing on splitting patterns and the integration of signals based on the surrounding hydrogen atoms.

Answered: Image /qna-images/answer/d08a643a-a6b2-4358-907f-823ef54e6a5e.jpg

Construct a simulated 'H NMR spectrum for 2-chloropropane. Drag and drop the appropriate splitting patterns into the boxes on the chemical shift baseline, and add integration values above each signal. Splitting patterns and integrations may be used more than once. Peak heights do not represent integration values. 7 CI 6 1H 5 4 Answer Bank DAD 4H 3 5H 2 6H 1 2H 0 ppm 3H

Construct a simulated 'H NMR spectrum for 2-chloropropane. Drag and drop the appropriate splitting patterns into the boxes on the chemical shift baseline, and add integration values above each signal. Splitting patterns and integrations may be used more than once. Peak heights do not represent integration values. 7 CI 6 1H 5 4 Answer Bank DAD 4H 3 5H 2 6H 1 2H 0 ppm 3H

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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Mass Spectrometry

This process is an instrumental method in which a sample is changed to fast moving positive ions by electron bombardment. The charged particles vary due to their different mass to charge ratio and are estimated with the help of this difference. It is also called mass spectroscopy.

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### Constructing a Simulated ¹H NMR Spectrum for 2-Chloropropane

**Objective:**
Create a simulated ¹H NMR spectrum for 2-chloropropane by assigning appropriate splitting patterns and integration values to the chemical shift baseline.

**Instructions:**
- Drag and drop the correct splitting patterns into the boxes on the chemical shift baseline.
- Add integration values above each signal.
- Splitting patterns and integrations may be reused as necessary.
- Note: Peak heights do not indicate integration values.

**Molecule:**
- The structure depicted is 2-chloropropane.

**Chemical Shift Baseline:**
- The x-axis is labeled with values from 7 ppm to 0 ppm.

**Answer Bank:**
- Options for splitting patterns and integration values:
- 1H
- 4H
- 5H
- 6H
- 2H
- 3H

**Graph Explanation:**
- Two main boxes are indicated along the chemical shift baseline.
- These boxes represent areas where you should place the splitting patterns from the answer bank.

**Integration and Splitting Patterns:**
- Match the splitting patterns and integration values to correctly simulate the NMR spectrum for 2-chloropropane. Consider the chemical environment and symmetry of hydrogen atoms in the molecule to determine the appropriate selections.

This exercise helps illustrate the principles of NMR spectroscopy, focusing on splitting patterns and the integration of signals based on the surrounding hydrogen atoms.

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