Find all the IR Peak Assignment and NMR Peak Assignment **Molecular Formula: C₄H₁₀O**### Graph Details#### Infrared (IR) Spectroscopy Graph:- **Y-axis**: % Transmittance- **X-axis**: Wavenumbers (cm⁻¹)Key Peaks:- Around **3500 cm⁻¹**: Broad dip indicating O-H stretching, common in alcohols.- Around **2900 cm⁻¹**: Indicating C-H stretching.- Around **1050 cm⁻¹**: Possibly indicating C-O stretching.The spectrum shows significant peaks that are characteristic of alcohol functional groups and hydrocarbon chains.#### Nuclear Magnetic Resonance (NMR) Spectrum:- **X-axis**: Chemical Shift (in ppm)- Detailed peaks are present from around **0.9 ppm** to **3.7 ppm**.- Notable Signals: - Multiple peaks around **1.0 ppm** indicate the presence of methyl groups. - Peaks around **3.5 ppm** suggest the presence of protons attached to oxygen (likely an alcohol group).This NMR spectrum corresponds to a molecule with hydrogens in different environments, characteristic of C₄H₁₀O. The peaks provide insight into the molecular structure, including the alkyl and hydroxyl groups.

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* TRANSMITTANCE Mol. fimula eo 60 4.0 4000 3.5 CH100 3339 3503 3000 Capillary film batuen salt plates 2 9.0 2500 HAVENUMBERS 2.5 2023 1471 137 1500 Page 1 of 1 W Page 1 of 1 1023 Copyright 1992 830.9 1.0 PPM

* TRANSMITTANCE Mol. fimula eo 60 4.0 4000 3.5 CH100 3339 3503 3000 Capillary film batuen salt plates 2 9.0 2500 HAVENUMBERS 2.5 2023 1471 137 1500 Page 1 of 1 W Page 1 of 1 1023 Copyright 1992 830.9 1.0 PPM

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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Question

Find all the IR Peak Assignment and NMR Peak Assignment

**Molecular Formula: C₄H₁₀O**

### Graph Details

#### Infrared (IR) Spectroscopy Graph:

- **Y-axis**: % Transmittance
- **X-axis**: Wavenumbers (cm⁻¹)

Key Peaks:
- Around **3500 cm⁻¹**: Broad dip indicating O-H stretching, common in alcohols.
- Around **2900 cm⁻¹**: Indicating C-H stretching.
- Around **1050 cm⁻¹**: Possibly indicating C-O stretching.

The spectrum shows significant peaks that are characteristic of alcohol functional groups and hydrocarbon chains.

#### Nuclear Magnetic Resonance (NMR) Spectrum:

- **X-axis**: Chemical Shift (in ppm)
- Detailed peaks are present from around **0.9 ppm** to **3.7 ppm**.
- Notable Signals:
- Multiple peaks around **1.0 ppm** indicate the presence of methyl groups.
- Peaks around **3.5 ppm** suggest the presence of protons attached to oxygen (likely an alcohol group).

This NMR spectrum corresponds to a molecule with hydrogens in different environments, characteristic of C₄H₁₀O. The peaks provide insight into the molecular structure, including the alkyl and hydroxyl groups.

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