3 attempts left Check my work Click the "draw structure" button to launch the drawing utility. The treatment of isoprene [CH,=C(CH3)CH=CH2] with one equivalent of mCPBA forms A as the -1 in major product. A gives a molecular ion at 84 in its mass spectrum, and peaks at 2850–3150 cm its IR spectrum. The 'H NMR spectrum of A is given below. What is the structure of A? H NMR of A ЗН 2 H 1H 2 H two doublets 8. 6. 4 2 1 ppm LO

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...
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Click the "draw structure" button to launch the drawing utility.
The treatment of isoprene [CH,=C(CH3)CH=CH2] with one equivalent of mCPBA forms A as the
ts
major product. A gives a molecular ion at 84 in its mass spectrum, and peaks at 2850–3150 cm in
its IR spectrum. The 'H NMR spectrum of A is given below. What is the structure of A?
еВook
1H NMR of A
3H
2 H
Print
1 H
2 H
eferences
two doublets
8
4
3
ppm
draw structure ..
-2-
中
Transcribed Image Text:12 3 attempts left Check my work Click the "draw structure" button to launch the drawing utility. The treatment of isoprene [CH,=C(CH3)CH=CH2] with one equivalent of mCPBA forms A as the ts major product. A gives a molecular ion at 84 in its mass spectrum, and peaks at 2850–3150 cm in its IR spectrum. The 'H NMR spectrum of A is given below. What is the structure of A? еВook 1H NMR of A 3H 2 H Print 1 H 2 H eferences two doublets 8 4 3 ppm draw structure .. -2- 中
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