Which of the following structures is consistent with the IR spectra shown below? % Transmittance 80 60 40 20 3500 3000 2500 2000 Wavenumbers (cm-1) 1500 1000 500

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...
icon
Related questions
Question
**Title: Interpretation of IR Spectra**

**Introduction:**
In infrared (IR) spectroscopy, a spectrum is used to identify the chemical structures of compounds based on their interaction with IR light. The spectrum depicts the percentage transmittance (% Transmittance) on the vertical axis against the wavenumbers (cm⁻¹) on the horizontal axis.

**Graph Description:**
- **X-Axis (Wavenumbers):** Ranges from 4000 to 500 cm⁻¹. Wavenumbers are a measure of frequency, and different functional groups absorb IR light at characteristic frequencies.
- **Y-Axis (% Transmittance):** Ranges from 0% to 100%. The higher the transmittance, the less light is absorbed at that wavelength.

**Main Observations:**
- **Broad peaks** around 3300 cm⁻¹, indicating N-H or O-H stretching vibrations, common in amines or alcohols.
- **Sharp peaks** near 1700 cm⁻¹, typically representative of C=O stretching vibrations, indicating the presence of a carbonyl group.
- **Multiple peaks** in the fingerprint region (1500-500 cm⁻¹) can correspond to complex bending and stretching modes of the molecule's structure.

**Conclusion:**
To identify the structure consistent with the IR spectrum, examine key absorption peaks, especially those indicating functional groups, and compare them with known reference spectra. This analysis helps in determining the molecular fingerprints of the compound being studied.
Transcribed Image Text:**Title: Interpretation of IR Spectra** **Introduction:** In infrared (IR) spectroscopy, a spectrum is used to identify the chemical structures of compounds based on their interaction with IR light. The spectrum depicts the percentage transmittance (% Transmittance) on the vertical axis against the wavenumbers (cm⁻¹) on the horizontal axis. **Graph Description:** - **X-Axis (Wavenumbers):** Ranges from 4000 to 500 cm⁻¹. Wavenumbers are a measure of frequency, and different functional groups absorb IR light at characteristic frequencies. - **Y-Axis (% Transmittance):** Ranges from 0% to 100%. The higher the transmittance, the less light is absorbed at that wavelength. **Main Observations:** - **Broad peaks** around 3300 cm⁻¹, indicating N-H or O-H stretching vibrations, common in amines or alcohols. - **Sharp peaks** near 1700 cm⁻¹, typically representative of C=O stretching vibrations, indicating the presence of a carbonyl group. - **Multiple peaks** in the fingerprint region (1500-500 cm⁻¹) can correspond to complex bending and stretching modes of the molecule's structure. **Conclusion:** To identify the structure consistent with the IR spectrum, examine key absorption peaks, especially those indicating functional groups, and compare them with known reference spectra. This analysis helps in determining the molecular fingerprints of the compound being studied.
Certainly! Below are transcriptions and detailed descriptions of the chemical structures depicted in the image:

1. **Cyclohexanone:**
   - The structure shows a six-membered carbon ring (cyclohexane) with a ketone functional group (C=O) attached to it. The ketone is located at one of the corners of the carbon ring.

2. **Phenol:**
   - This molecule consists of a six-membered aromatic benzene ring with an -OH (hydroxyl group) attached. The benzene ring is depicted with alternating double bonds, indicating aromaticity.

3. **Isobutyronitrile:**
   - The structure illustrates a three-carbon chain with a nitrile group (C≡N) attached to the second carbon. The carbon atoms are connected in a branch-like structure, resembling an isobutyl group.

4. **Acetophenone:**
   - This molecule has a benzene ring attached to a carbonyl group (C=O) which is further attached to a methyl group (CH₃). The carbonyl and methyl groups together form an acetyl group linked to the benzene.

5. **Pentanal:**
   - The structure represents a straight five-carbon chain with an aldehyde group (C=O with an H atom) at the end. The aldehyde functionality is indicated by the carbonyl group connected to a terminal hydrogen atom.

Each structure represents various functional groups and types of chemical bonding, serving as fundamental examples for understanding organic chemistry on an educational platform.
Transcribed Image Text:Certainly! Below are transcriptions and detailed descriptions of the chemical structures depicted in the image: 1. **Cyclohexanone:** - The structure shows a six-membered carbon ring (cyclohexane) with a ketone functional group (C=O) attached to it. The ketone is located at one of the corners of the carbon ring. 2. **Phenol:** - This molecule consists of a six-membered aromatic benzene ring with an -OH (hydroxyl group) attached. The benzene ring is depicted with alternating double bonds, indicating aromaticity. 3. **Isobutyronitrile:** - The structure illustrates a three-carbon chain with a nitrile group (C≡N) attached to the second carbon. The carbon atoms are connected in a branch-like structure, resembling an isobutyl group. 4. **Acetophenone:** - This molecule has a benzene ring attached to a carbonyl group (C=O) which is further attached to a methyl group (CH₃). The carbonyl and methyl groups together form an acetyl group linked to the benzene. 5. **Pentanal:** - The structure represents a straight five-carbon chain with an aldehyde group (C=O with an H atom) at the end. The aldehyde functionality is indicated by the carbonyl group connected to a terminal hydrogen atom. Each structure represents various functional groups and types of chemical bonding, serving as fundamental examples for understanding organic chemistry on an educational platform.
Expert Solution
steps

Step by step

Solved in 3 steps with 7 images

Blurred answer
Knowledge Booster
Nuclear Magnetic Resonance
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY