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Chemistry / Organic Chemistry 7 / Chapter 15 / Problem 74P

Organic Chemistry | 7th Edition | ISBN: 9781269406772 | Authors: Paula Yurkanis Bruice

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When compound A (C5H12O) is treated with HBr, it forms

Chapter 15, Problem 74P

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Problem 74P

When compound A (C5H12O) is treated with HBr, it forms compound B (C5H11Br). The 1H NMR spectrum of compound A has one singlet (1), two doublets (3, 6), and two multiplets (both 1). (The relative areas of the signals are indicated in parentheses.) The 1H NMR spectrum of compound B has a singlet (6), a triplet (3), and a quartet (2). Identify compounds A and B.

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QUESTION:

Problem 74P

When compound A (C5H12O) is treated with HBr, it forms compound B (C5H11Br). The 1H NMR spectrum of compound A has one singlet (1), two doublets (3, 6), and two multiplets (both 1). (The relative areas of the signals are indicated in parentheses.) The 1H NMR spectrum of compound B has a singlet (6), a triplet (3), and a quartet (2). Identify compounds A and B.

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