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

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

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter18: Ethers And Epoxides; Thiols And Sulfides

Section18.SE: Something Extra

Problem 54AP: Anethole, C10H12O, a major constituent of the oil of anise, has the 1H NMR spectrum shown. On...

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