What functional group had one peak that did not show up in the table of wavenumbers under the spectrum? What is the bond (including both atoms and bond order) and expected approximate wavenumber of this peak?

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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### Transcription and Analysis of Spectroscopy Data

#### Title: Infrared Spectroscopy Analysis of 2-Octenoic Acid

**Chemical Structure:**
The chemical structure displayed is for 2-Octenoic acid. It contains a chain of carbon atoms with the following composition:
- Chemical formula: \( C_8H_{14}O_2 \)
- Skeletal representation: 
  \[
  \text{CH}_3 \text{--(CH}_2\text{)$_4$---CH=CH--COOH}
  \]

**Graph Overview:**
- **Type of Graph:** Infrared (IR) Spectroscopy
- **Axis Details:**
  - **Horizontal Axis (x-axis):** Represents Wavenumber (\(\text{cm}^{-1}\)), ranging from approximately 700 to 4000 \(\text{cm}^{-1}\).
  - **Vertical Axis (y-axis):** Represents Transmittance (%), varying from 0% to 100%.

**Spectral Peaks and Explanation:**
Several peaks are observable across the spectrum representing specific bond vibrations:

1. **High Wavenumber Region (above 3000 cm\(^{-1}\)):**
   - **Broad Peak:** Suggests the presence of O-H stretching, typical in carboxylic acids.

2. **Mid-Wavenumber Region (2000 to 1500 cm\(^{-1}\)):**
   - **Sharp Peak around 1700 cm\(^{-1}\):** Indicates C=O stretching, characteristic of carboxylic acids.

3. **Low Wavenumber Region (below 1500 cm\(^{-1}\)):**
   - Multiple smaller peaks represent various C-H and C-O bond bending and stretching vibrations.

**Data Table:**
- Contains numerical values, presumably absorption or transmittance at specific wavenumbers. These help in quantitatively analyzing specific bond absorption characteristics, although these values are not explicitly readable in the image provided.

#### Practical Implications:
Understanding this spectrum is crucial for identifying functional groups within the compound and verifying its molecular structure as 2-Octenoic Acid. This analysis is integral to fields like organic chemistry and pharmaceuticals where molecular identification is pivotal.
Transcribed Image Text:### Transcription and Analysis of Spectroscopy Data #### Title: Infrared Spectroscopy Analysis of 2-Octenoic Acid **Chemical Structure:** The chemical structure displayed is for 2-Octenoic acid. It contains a chain of carbon atoms with the following composition: - Chemical formula: \( C_8H_{14}O_2 \) - Skeletal representation: \[ \text{CH}_3 \text{--(CH}_2\text{)$_4$---CH=CH--COOH} \] **Graph Overview:** - **Type of Graph:** Infrared (IR) Spectroscopy - **Axis Details:** - **Horizontal Axis (x-axis):** Represents Wavenumber (\(\text{cm}^{-1}\)), ranging from approximately 700 to 4000 \(\text{cm}^{-1}\). - **Vertical Axis (y-axis):** Represents Transmittance (%), varying from 0% to 100%. **Spectral Peaks and Explanation:** Several peaks are observable across the spectrum representing specific bond vibrations: 1. **High Wavenumber Region (above 3000 cm\(^{-1}\)):** - **Broad Peak:** Suggests the presence of O-H stretching, typical in carboxylic acids. 2. **Mid-Wavenumber Region (2000 to 1500 cm\(^{-1}\)):** - **Sharp Peak around 1700 cm\(^{-1}\):** Indicates C=O stretching, characteristic of carboxylic acids. 3. **Low Wavenumber Region (below 1500 cm\(^{-1}\)):** - Multiple smaller peaks represent various C-H and C-O bond bending and stretching vibrations. **Data Table:** - Contains numerical values, presumably absorption or transmittance at specific wavenumbers. These help in quantitatively analyzing specific bond absorption characteristics, although these values are not explicitly readable in the image provided. #### Practical Implications: Understanding this spectrum is crucial for identifying functional groups within the compound and verifying its molecular structure as 2-Octenoic Acid. This analysis is integral to fields like organic chemistry and pharmaceuticals where molecular identification is pivotal.
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