Partial Question 4 2/6 What type of oxygen-based functional groups may be present in the molecule, based on the IR? Can the molecule contain a/an: aldehyde? No alcohol? No carboxylic acid? Yes ester? No ether? No ketone? No

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
**Question 4**

*What type of oxygen-based functional groups may be present in the molecule, based on the IR? Can the molecule contain a/an:*

- Aldehyde? No
- Alcohol? No
- Carboxylic acid? Yes
- Ester? No
- Ether? No
- Ketone? No

**Explanation:**

Infrared (IR) spectroscopy is a technique used to identify functional groups in molecules based on their vibrational transitions. In this instance, the analysis indicates the presence of a carboxylic acid group, as identified by its characteristic absorption patterns in the IR spectrum. Other functional groups such as aldehyde, alcohol, ester, ether, and ketone do not exhibit the expected IR absorption features, leading to a negative confirmation for their presence.
Transcribed Image Text:**Question 4** *What type of oxygen-based functional groups may be present in the molecule, based on the IR? Can the molecule contain a/an:* - Aldehyde? No - Alcohol? No - Carboxylic acid? Yes - Ester? No - Ether? No - Ketone? No **Explanation:** Infrared (IR) spectroscopy is a technique used to identify functional groups in molecules based on their vibrational transitions. In this instance, the analysis indicates the presence of a carboxylic acid group, as identified by its characteristic absorption patterns in the IR spectrum. Other functional groups such as aldehyde, alcohol, ester, ether, and ketone do not exhibit the expected IR absorption features, leading to a negative confirmation for their presence.
The image displays an infrared (IR) spectrum graph for a substance labeled "Unknown C NEAT." The x-axis represents the wavenumber in cm⁻¹ (ranging from 4000 to 450 cm⁻¹), which is inversely proportional to wavelength, while the y-axis shows the percent transmittance (%T), ranging from 45% to 102%.

Key absorption peaks are labeled with their corresponding wavenumbers:

- **2958.34 cm⁻¹** and **2873.37 cm⁻¹**: These peaks typically indicate C-H stretching vibrations.
- **1737.03 cm⁻¹**: This peak is often associated with C=O stretching, common in carbonyl groups.
- **1467.20 cm⁻¹** and **1436.10 cm⁻¹**: These peaks may correspond to bending vibrations of CH₂ groups.
- **1368.59 cm⁻¹** and **1256.23 cm⁻¹**: These are characteristic of C-H bending.
- **1194.38 cm⁻¹**, **1157.32 cm⁻¹**, and **1121.14 cm⁻¹**: These likely represent C-O stretching vibrations.
- **1011.55 cm⁻¹**, **1100.85 cm⁻¹**, and **881.86 cm⁻¹**: These can indicate out-of-plane bending for aromatic compounds or ring structures.
- **830.91 cm⁻¹**, **711.23 cm⁻¹**, and **592.08 cm⁻¹**: Peaks in this region often suggest C-H bending or wagging modes, especially in substituted rings.
- **553.75 cm⁻¹**: This may indicate skeletal vibrations of the molecular structure.

The graph is useful for identifying functional groups based on the IR absorption characteristics of the unknown compound.
Transcribed Image Text:The image displays an infrared (IR) spectrum graph for a substance labeled "Unknown C NEAT." The x-axis represents the wavenumber in cm⁻¹ (ranging from 4000 to 450 cm⁻¹), which is inversely proportional to wavelength, while the y-axis shows the percent transmittance (%T), ranging from 45% to 102%. Key absorption peaks are labeled with their corresponding wavenumbers: - **2958.34 cm⁻¹** and **2873.37 cm⁻¹**: These peaks typically indicate C-H stretching vibrations. - **1737.03 cm⁻¹**: This peak is often associated with C=O stretching, common in carbonyl groups. - **1467.20 cm⁻¹** and **1436.10 cm⁻¹**: These peaks may correspond to bending vibrations of CH₂ groups. - **1368.59 cm⁻¹** and **1256.23 cm⁻¹**: These are characteristic of C-H bending. - **1194.38 cm⁻¹**, **1157.32 cm⁻¹**, and **1121.14 cm⁻¹**: These likely represent C-O stretching vibrations. - **1011.55 cm⁻¹**, **1100.85 cm⁻¹**, and **881.86 cm⁻¹**: These can indicate out-of-plane bending for aromatic compounds or ring structures. - **830.91 cm⁻¹**, **711.23 cm⁻¹**, and **592.08 cm⁻¹**: Peaks in this region often suggest C-H bending or wagging modes, especially in substituted rings. - **553.75 cm⁻¹**: This may indicate skeletal vibrations of the molecular structure. The graph is useful for identifying functional groups based on the IR absorption characteristics of the unknown compound.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 3 steps

Blurred answer
Knowledge Booster
Mass Spectrometry
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