Organic Chemistry (6th Edition)
Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
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Chapter 12C, Problem 68P

Reaction of aldehyde D with amino alcohol E in the presence of NaH forms F (molecular formula C 11 H 15 NO 2 ). F absorbs at 1730 cm 1 in its IR spectrum. F also shows eight lines in its 13 C NMR spectrum, and gives the following 1 H NMR spectrum: 2 .32 ( sin glet 6 H ) , 3 .05 ( triplet, 2 H ) , 4 .20 ( triplet, 2 H ) , 6 .97 ( doublet, 2 H ) , 7.82 ( doublet, 2 H ) and 9 .97 ( singlet, 1 H ) ppm . Propose a structure for F. We will learn about this reaction in Chapter 18.

Chapter 12C, Problem 68P, Reaction of aldehyde D with amino alcohol E in the presence of NaH forms F molecular formula

D E

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Reaction of aldehyde D with amino alcohol E in the presence of NaH forms F (molecular formula C11H15NO2). F absorbs at 1730 cm−1 in its IR spectrum. F also shows eight lines in its 13C NMR spectrum, and gives the following 1H NMR spectrum: 2.32 (singlet, 6 H), 3.05 (triplet, 2 H), 4.20 (triplet, 2 H), 6.97 (doublet, 2 H), 7.82 (doublet, 2 H), and 9.97 (singlet, 1 H) ppm. Propose a structure for F. We will learn about this reaction in Chapter 18.
Reaction of p-cresol with two equivalents of 2-methylprop-1-ene affords BHT, a preservative with molecular formula C15H24O. BHT gives the following 1H NMR spectral data: 1.4 (singlet, 18 H), 2.27 (singlet, 3 H), 5.0 (singlet, 1 H), and 7.0 (singlet, 2 H) ppm. What is the structure of BHT? Draw a stepwise mechanism illustrating how it is formed.
When heated with an acidic solution of sodium dichromate, compound A forms benzoic acid. Identify compound A from its 1H NMR spectrum. Note: The ppm values for the multiplet shown in the inset ranges from 2.8-3.0 ppm and not 1.1-1.3 ppm as shown.

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Organic Chemistry (6th Edition)

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