In this ¹H NMR spectrum the blue floating peaks are enlargements of the peaks to their right. 10.0 9.0 8.0 wwwwwwwww 44 7.0 4.3 30 20 100 Hz 6.0 4.2 ppm 5.0 4.0 Hull 1.75 1.70 1.6 3.0 2.0 1.0 0.0 Which compound is most likely to have given rise to this spectrum?

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
icon
Concept explainers
Question
-COH (acid)
&H (aldehyde)
Ar-H (aromatic)
(C=C-H, vinylic
OH (alcohol or phenol)
X-C-H (X= halogen or oxygen)
Ar-C-H (benzylic)
CH
10.0
(C-C-C-H, allylic
H on saturated C, base position
9.0
8.0
44
7.0
4.3
30 20 10 0
6.0
In this ¹H NMR spectrum the blue floating peaks are enlargements of the peaks to their right.
4.2
ppm
Hz
5.0
1
4.0
10-13
9-10
3.0
6-8.5
4.6-5.7)
1-5
3-4.5
2-2.7
2-2.7
1.6-1.9)
.8-1.6
l
1.75 1.70 1.65
2.0
1.0
0.0
Which compound is most likely to have given rise to this spectrum?
Transcribed Image Text:-COH (acid) &H (aldehyde) Ar-H (aromatic) (C=C-H, vinylic OH (alcohol or phenol) X-C-H (X= halogen or oxygen) Ar-C-H (benzylic) CH 10.0 (C-C-C-H, allylic H on saturated C, base position 9.0 8.0 44 7.0 4.3 30 20 10 0 6.0 In this ¹H NMR spectrum the blue floating peaks are enlargements of the peaks to their right. 4.2 ppm Hz 5.0 1 4.0 10-13 9-10 3.0 6-8.5 4.6-5.7) 1-5 3-4.5 2-2.7 2-2.7 1.6-1.9) .8-1.6 l 1.75 1.70 1.65 2.0 1.0 0.0 Which compound is most likely to have given rise to this spectrum?
Expert Solution
Step 1

Way of approach to solve the given question: The knowledge of chemical shift and splitting of peaks in nmr is necessary to solve the given question.

Chemical shift: The difference between resonance frequency of a observed proton and the standard trimethylsilane(TMS) is known as chemical shift.

The chemical shift increases with increasing electronegativity of adjacent groups or increases with the presence of adjacent electron withdrawing groups.

i.e. The chemical shift of observed proton directly proportional to the electronegativity and electron withdrawing nature of adjacent groups.

Splitting of nmr peaks:

The splitting of peaks follow (n+1) rule. here, n= the no. of adjacent protons.

Adjacent protons (n+1) rule splitting of signal
0 0+1=1 singlet
1 1+1=2 doublet
2 2+1=3 triplet
3 3+1=4 quarte
4 4+1=5 quintet
5 5+1=6 sextet
6 6+1=7 septet
steps

Step by step

Solved in 2 steps with 1 images

Blurred answer
Knowledge Booster
IR 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.
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