LOD NH 500 L000 4 D00 3000 2000 1500 HAVENUMB ERI 1l 50 4 D00 3000 2000 15 00 1000 5 DO HAVENUMB ERI -1 TPANSHETTRNC EI

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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Can someone please help me with this? I just need labeling the important peaks with the corresponding functional group and justify why its that

### Infrared Spectroscopy Analysis

#### Figure 1: Infrared Spectrum of an Aliphatic Amine

- **X-Axis (Wavenumber cm⁻¹):** The spectrum spans from about 4000 cm⁻¹ to 500 cm⁻¹.
- **Y-Axis (Transmittance %):** Indicates the transmittance of infrared light through the sample.
- **Prominent Peaks:**
  - Broad peak around 3300 cm⁻¹, typical for N-H stretching in amines.
  - Peaks near 2800-3000 cm⁻¹, characteristic of C-H stretching in alkanes.
  - Other peaks observed between 1500-1000 cm⁻¹, which may correspond to C-N stretching.

#### Figure 2: Infrared Spectrum of an Aromatic Ester

- **X-Axis (Wavenumber cm⁻¹):** Again, the spectrum ranges from 4000 cm⁻¹ to 500 cm⁻¹.
- **Y-Axis (Transmittance %):** Shows the transmittance of the sample.
- **Prominent Peaks:**
  - Peak near 1700 cm⁻¹, indicative of C=O stretching in esters.
  - Peaks around 3000 cm⁻¹, associated with aromatic C-H stretching.
  - Complex pattern of peaks between 1500-1000 cm⁻¹, related to C=C stretching and other vibrational modes of the aromatic ring and ester functional group.

#### Summary
Both spectra display the characteristic functional group absorptions that help in identifying substances based on their molecular vibrations. The first spectrum is indicative of an aliphatic amine, while the second one corresponds to an aromatic ester.
Transcribed Image Text:### Infrared Spectroscopy Analysis #### Figure 1: Infrared Spectrum of an Aliphatic Amine - **X-Axis (Wavenumber cm⁻¹):** The spectrum spans from about 4000 cm⁻¹ to 500 cm⁻¹. - **Y-Axis (Transmittance %):** Indicates the transmittance of infrared light through the sample. - **Prominent Peaks:** - Broad peak around 3300 cm⁻¹, typical for N-H stretching in amines. - Peaks near 2800-3000 cm⁻¹, characteristic of C-H stretching in alkanes. - Other peaks observed between 1500-1000 cm⁻¹, which may correspond to C-N stretching. #### Figure 2: Infrared Spectrum of an Aromatic Ester - **X-Axis (Wavenumber cm⁻¹):** Again, the spectrum ranges from 4000 cm⁻¹ to 500 cm⁻¹. - **Y-Axis (Transmittance %):** Shows the transmittance of the sample. - **Prominent Peaks:** - Peak near 1700 cm⁻¹, indicative of C=O stretching in esters. - Peaks around 3000 cm⁻¹, associated with aromatic C-H stretching. - Complex pattern of peaks between 1500-1000 cm⁻¹, related to C=C stretching and other vibrational modes of the aromatic ring and ester functional group. #### Summary Both spectra display the characteristic functional group absorptions that help in identifying substances based on their molecular vibrations. The first spectrum is indicative of an aliphatic amine, while the second one corresponds to an aromatic ester.
**Infrared Spectroscopy Analysis Assignment**

**Objective:** Assign the major peaks in each spectrum. 

**Instructions:**

1. **Match the following structures to the correct IR spectrum by drawing the structure on the spectrum.**
2. **Label all important peaks with the corresponding functional groups.**

**IMPORTANT:** Draw the corresponding matching structure in the boxed spectrum.

**Structures Provided:**

- **Structure 1:** Ether
- **Structure 2:** Phenol
- **Structure 3:** Ketone
- **Structure 4:** Ester
- **Structure 5:** Alcohol
- **Structure 6:** Amine

**IR Spectrum Analysis:**

- The x-axis represents the **wavenumber (\(cm^{-1}\))**, ranging from 4000 to 500.
- The y-axis represents the **transmittance percentage (%T)** from 0 to 100.

**Key Peaks:**

- **Around 3300 cm\(^{-1}\):** Possibly indicating N-H or O-H stretching.
- **Around 1700 cm\(^{-1}\):** Characteristic of C=O stretching in ketones or esters.
- **Below 1600 cm\(^{-1}\):** Multiple peaks possibly due to C=C, C-O, or other functional groups.

**Task:**

Identify and match the given structures with the IR spectrum by analyzing the presence of specific functional group peaks and draw the correct structure on the spectrum.

**Please justify your structure choice** by explaining which functional groups are responsible for the observed peaks.
Transcribed Image Text:**Infrared Spectroscopy Analysis Assignment** **Objective:** Assign the major peaks in each spectrum. **Instructions:** 1. **Match the following structures to the correct IR spectrum by drawing the structure on the spectrum.** 2. **Label all important peaks with the corresponding functional groups.** **IMPORTANT:** Draw the corresponding matching structure in the boxed spectrum. **Structures Provided:** - **Structure 1:** Ether - **Structure 2:** Phenol - **Structure 3:** Ketone - **Structure 4:** Ester - **Structure 5:** Alcohol - **Structure 6:** Amine **IR Spectrum Analysis:** - The x-axis represents the **wavenumber (\(cm^{-1}\))**, ranging from 4000 to 500. - The y-axis represents the **transmittance percentage (%T)** from 0 to 100. **Key Peaks:** - **Around 3300 cm\(^{-1}\):** Possibly indicating N-H or O-H stretching. - **Around 1700 cm\(^{-1}\):** Characteristic of C=O stretching in ketones or esters. - **Below 1600 cm\(^{-1}\):** Multiple peaks possibly due to C=C, C-O, or other functional groups. **Task:** Identify and match the given structures with the IR spectrum by analyzing the presence of specific functional group peaks and draw the correct structure on the spectrum. **Please justify your structure choice** by explaining which functional groups are responsible for the observed peaks.
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