The MS and 13C NMR spectra for two constitutional isomers are shown. They have 4 degrees of unsaturation. Determine the molecular structures of the two constitutional isomers. ISOMER AISOMER B100-10080-80-60-60-40 -40-MT. 14020-20-75100125255075100125m/zm/zm? pautas total2 peaks3 peales tolad2001801601401201008060402020018016014012010080604020CDS-00-007ppmCos-00-e86pmRelative IntensityRelative Intensity

Answered: Image /qna-images/answer/cccefef5-2a40-4c42-a473-54eea4869e50.jpg

Answered: दो संवैधानिक समावयवों के लिए MS और 13C…

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

Related questions

Concept explainers

Question

The MS and 13C NMR spectra for two constitutional isomers are shown. They have 4 degrees of unsaturation. Determine the molecular structures of the two constitutional isomers.

ISOMER A
ISOMER B
100-
100
80-
80-
60-
60-
40 -
40-
MT. 140
20-
20-
75
100
125
25
50
75
100
125
m/z
m/z
m? pautas total
2 peaks
3 peales tolad
200
180
160
140
120
100
80
60
40
20
200
180
160
140
120
100
80
60
40
20
CDS-00-007
ppm
Cos-00-e86
pm
Relative Intensity
Relative Intensity

Expert Solution

Step by step

Solved in 2 steps with 2 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

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