Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card
Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card
9th Edition
ISBN: 9781305780170
Author: John E. McMurry
Publisher: Cengage Learning
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Chapter 29.SE, Problem 56AP
Interpretation Introduction

Interpretation:

A hydride from NADPH adds to C3 of the crotonyl group from the Re face, and protonation on C2 occurs on the Si face. To explain the reduction a syn addition or an anti addition.

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From Table 1.1 indicates, among other things, the melting points of various fatty acids. Analyze the trend that the melting points of saturated fatty acids follow, from n-dodecanoic (CH3-(CH2) 10-COOH) to n-tetracosanoic (CH3-(CH2)22-COOH), and answer both next questions. Briefly justify your answers. i) What value would you expect the melting point of triacontanoic acid (CH3-(CH2) 28-COOH) to have? Choose one of the following options:a) More than 200 ° Cb) About 94 ° Cc) Less than 86 ° Cd) Exactly 86.1 ° C ii) What value would you expect the melting point of octanoic acid (CH3-(CH2) 6-COOH) to have? Choose one of the following options:a) 43.5 ° Cb) -20 ° Cc) About 20 ° C
What is the melting point order of the following fatty acids (lowest to highest), the ratio in parenthesis is single bonds to double bonds. Lauric (12:0), Palmitic (16:0), Palmitoleic (16:1), and Oleic (18:1).
Compute the RER derived from the oxidation of palmitic acid. CH3(CH2)14COOH + 23O2 → 16CO2 + 16H2O

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Bundle: Organic Chemistry, Loose-leaf Version, 9th + LMS Integrated for OWLv2, 4 terms (24 months) Printed Access Card

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