Homework Help is Here – Start Your Trial Now!
Science
Chemistry
C10H14 5H 2H ulunluululumbuun 1.4 i2 2H 2H Í PPM

C10H14 5H 2H ulunluululumbuun 1.4 i2 2H 2H Í PPM

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

please help detail the mass spectrum

### Spectroscopy Assignment #### NMR Spectroscopy Analysis of C₁₀H₁₄ and C₅H₁₂O The image presents two Nuclear Magnetic Resonance (NMR) spectra for two different organic compounds, denoted as C₁₀H₁₄ and C₅H₁₂O. #### Compound 1: C₁₀H₁₄ - **Chemical Shifts and Integrations:** - 7.0 - 6.5 ppm: A large peak with an integration of 5H, likely representing aromatic hydrogens. - 2.1 - 1.4 ppm: Several peaks with integrations annotated with "t", "2H", indicating splitting patterns and hydrogen counts. - 1.0 ppm: A triplet (t) with an integration of 3H, typically indicative of a terminal methyl group (-CH₃). - **Inset:** - An enlarged view of the 5.6 - 1.2 ppm region provides a closer look at the splitting patterns, revealing more detailed information about the hydrogen environments in this range. #### Compound 2: C₅H₁₂O - **Chemical Shifts and Integrations:** - 3.3 ppm: A singlet (1H) likely corresponding to a proton adjacent to an oxygen atom (e.g., -OH). - 1.7 - 1.5 ppm: Multiple peaks with integrations of 2H and 3H, suggesting multiple hydrogen environments, possibly adjacent to alkyl groups. - 0.9 ppm: A large peak with an integration of 6H, indicating the presence of two equivalent methyl groups. #### Graphs and Diagrams: - The upper graph displays the NMR spectrum for C₁₀H₁₄, featuring a range from 0 to 7.8 ppm. Peaks are annotated with hydrogen counts and splitting patterns. - The lower graph shows the NMR spectrum for C₅H₁₂O, also annotated with chemical shifts and integrals, ranging from 0 to 3.3 ppm. Peaks are labeled with the number of hydrogen atoms they represent. Both spectra offer insight into the molecular structure of the respective compounds, highlighting the variety of hydrogen environments and the splitting patterns due to neighboring hydrogen atoms. ### Conclusion
Transcribed Image Text:### Spectroscopy Assignment #### NMR Spectroscopy Analysis of C₁₀H₁₄ and C₅H₁₂O The image presents two Nuclear Magnetic Resonance (NMR) spectra for two different organic compounds, denoted as C₁₀H₁₄ and C₅H₁₂O. #### Compound 1: C₁₀H₁₄ - **Chemical Shifts and Integrations:** - 7.0 - 6.5 ppm: A large peak with an integration of 5H, likely representing aromatic hydrogens. - 2.1 - 1.4 ppm: Several peaks with integrations annotated with "t", "2H", indicating splitting patterns and hydrogen counts. - 1.0 ppm: A triplet (t) with an integration of 3H, typically indicative of a terminal methyl group (-CH₃). - **Inset:** - An enlarged view of the 5.6 - 1.2 ppm region provides a closer look at the splitting patterns, revealing more detailed information about the hydrogen environments in this range. #### Compound 2: C₅H₁₂O - **Chemical Shifts and Integrations:** - 3.3 ppm: A singlet (1H) likely corresponding to a proton adjacent to an oxygen atom (e.g., -OH). - 1.7 - 1.5 ppm: Multiple peaks with integrations of 2H and 3H, suggesting multiple hydrogen environments, possibly adjacent to alkyl groups. - 0.9 ppm: A large peak with an integration of 6H, indicating the presence of two equivalent methyl groups. #### Graphs and Diagrams: - The upper graph displays the NMR spectrum for C₁₀H₁₄, featuring a range from 0 to 7.8 ppm. Peaks are annotated with hydrogen counts and splitting patterns. - The lower graph shows the NMR spectrum for C₅H₁₂O, also annotated with chemical shifts and integrals, ranging from 0 to 3.3 ppm. Peaks are labeled with the number of hydrogen atoms they represent. Both spectra offer insight into the molecular structure of the respective compounds, highlighting the variety of hydrogen environments and the splitting patterns due to neighboring hydrogen atoms. ### Conclusion
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 1 images

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
Atoms
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