Homework Help is Here – Start Your Trial Now!
Science
Chemistry
100 80 60 40 20 0.0 Naphthalene, 2-butoxy- El mass spectrum, top peaks displayed

100 80 60 40 20 0.0 Naphthalene, 2-butoxy- El mass spectrum, top peaks displayed

Chemistry
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...
See similar textbooks
icon
Related questions
Question

Identify the peaks for compound of 2-Naphthyl-Butylether. 

**Mass Spectrum Analysis: Naphthalene, 2-butoxy-** This graph represents the Electron Ionization (EI) mass spectrum of naphthalene, 2-butoxy-, highlighting the most significant peaks. The horizontal axis represents the mass-to-charge ratio (m/z), ranging from 100 to 220, while the vertical axis indicates the abundance of ions, with a maximum value of 100. **Peak Analysis:** 1. **Peak at m/z ~110**: - This peak has a low relative abundance indicating a minor fragment. 2. **Peak at m/z ~140**: - This is the most prominent peak with an abundance of 100, suggesting the presence of a major fragment or the molecular ion. 3. **Peak at m/z ~200**: - Another noticeable peak with moderate abundance, indicating the presence of a significant fragment. Understanding these peaks helps in identifying the structural components and molecular weight of the compound being analyzed. The most intense peak often represents the base peak, which can be crucial for determining compound identity in mass spectrometry.
Transcribed Image Text:**Mass Spectrum Analysis: Naphthalene, 2-butoxy-** This graph represents the Electron Ionization (EI) mass spectrum of naphthalene, 2-butoxy-, highlighting the most significant peaks. The horizontal axis represents the mass-to-charge ratio (m/z), ranging from 100 to 220, while the vertical axis indicates the abundance of ions, with a maximum value of 100. **Peak Analysis:** 1. **Peak at m/z ~110**: - This peak has a low relative abundance indicating a minor fragment. 2. **Peak at m/z ~140**: - This is the most prominent peak with an abundance of 100, suggesting the presence of a major fragment or the molecular ion. 3. **Peak at m/z ~200**: - Another noticeable peak with moderate abundance, indicating the presence of a significant fragment. Understanding these peaks helps in identifying the structural components and molecular weight of the compound being analyzed. The most intense peak often represents the base peak, which can be crucial for determining compound identity in mass spectrometry.
This image depicts the chemical structure of 2-butoxynaphthalene. ### Description: - **Naphthalene Core**: The structure features two fused benzene rings, forming the naphthalene core. This is the aromatic hydrocarbon base of the compound. - **Butoxy Group**: Attached to the naphthalene core is a butoxy group. This group is composed of a butyl chain (four carbon atoms in length) connected via an ether linkage (an oxygen atom). ### Chemical Bonds: - **Carbon-Carbon (C-C) Bonds**: Present within the benzene rings and the butyl chain. - **Carbon-Oxygen (C-O) Bond**: This ether bond connects the naphthalene to the butyl chain. ### Orientation: - The butoxy group is at the 2-position of the naphthalene ring, meaning it is attached to the second carbon atom relative to a reference point on the naphthalene. This structure is often used in educational settings to demonstrate aromatic compounds and ethers in organic chemistry.
Transcribed Image Text:This image depicts the chemical structure of 2-butoxynaphthalene. ### Description: - **Naphthalene Core**: The structure features two fused benzene rings, forming the naphthalene core. This is the aromatic hydrocarbon base of the compound. - **Butoxy Group**: Attached to the naphthalene core is a butoxy group. This group is composed of a butyl chain (four carbon atoms in length) connected via an ether linkage (an oxygen atom). ### Chemical Bonds: - **Carbon-Carbon (C-C) Bonds**: Present within the benzene rings and the butyl chain. - **Carbon-Oxygen (C-O) Bond**: This ether bond connects the naphthalene to the butyl chain. ### Orientation: - The butoxy group is at the 2-position of the naphthalene ring, meaning it is attached to the second carbon atom relative to a reference point on the naphthalene. This structure is often used in educational settings to demonstrate aromatic compounds and ethers in organic chemistry.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 3 steps with 1 images

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
NMR Spectroscopy of Organic Molecules
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.
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
SEE MORE TEXTBOOKS