Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card
5th Edition
ISBN: 9781260170405
Author: SMITH
Publisher: MCG
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Chapter 31, Problem 31.21P
Interpretation Introduction
Interpretation: The possible constitutional isomers of as triacylglycerol formed from one mole of each palmitic acid, oleic and linoleic acid are to be drawn and the stereogenic centers are to be located in each constitutional isomer.
Concept introduction: Triacylglycerols are a type of lipids. They are composed of three fatty acids and glycerol. Simple triacylglycerol contains three same fatty acids while mixed triacylglycerol contains two or more different fatty acids. They are also known as triglycerides.
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Stearidonic acid (C18H28O2) is an unsaturated fatty acid obtained fromoils isolated from hemp and blackcurrant
a.) What fatty acid is formed when stearidonic acid is hydrogenated withexcess H2 and a Pd catalyst?b.) What fatty acids are formed when stearidonic acid is hydrogenatedwith one equivalent of H2 and a Pd catalyst?c.) Draw the structure of a possible product formed when stearidonic acidis hydrogenated with one equivalent of H2 and a Pd catalyst, and onedouble bond is isomerized to a trans isomer.d.) How do the melting points of the following fatty acids compare:stearidonic acid; one of the products formed in part (b); the productdrawn in part (c)?
A simple triacylglycerol is one that:
a) Upon hydrolysis produces glycerol and three different fatty acids.
b) Upon hydrolysis produces glycerol and at least two different fatty acids.
c) Upon saponification gives glycerol and three fatty acid salts.
d) Upon saponification gives three esters.
e) Upon hydrolysis produces glycerol and three mol of a fatty acid.
Triacylglycerides obtained from animal fats and plant oils are typically used in the production of biodiesel. Explain the advantage of using a triacylglyceride as the starting material for biodiesel synthesis over the waxy esters found in Jojoba oil.
Chapter 31 Solutions
Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card
Ch. 31 - Problem 31.1
One component of jojoba oil is a wax...Ch. 31 - Problem 31.2
How would you expect the melting...Ch. 31 - Problem 31.3
Draw the products formed when...Ch. 31 - Problem 31.4
The main fatty acid component of the...Ch. 31 - Prob. 31.5PCh. 31 - Problem 31.6
Draw the structure of a lecithin...Ch. 31 - Prob. 31.7PCh. 31 - Problem 31.8
Why are phospholipids, but not...Ch. 31 - Problem 31.9
Explain why regularly ingesting a...Ch. 31 - Problem 31.10
Locate the isoprene units in each...
Ch. 31 - Problem 31.11
Locate the isoprene units in...Ch. 31 - Problem 31.12
Write a stepwise mechanism for the...Ch. 31 - Prob. 31.13PCh. 31 - Prob. 31.14PCh. 31 - Prob. 31.15PCh. 31 - Prob. 31.16PCh. 31 - 31.17 Locate the isoprene units in each...Ch. 31 - Prob. 31.18PCh. 31 - Prob. 31.19PCh. 31 - Prob. 31.20PCh. 31 - Prob. 31.21PCh. 31 - 31.22 What is the structure of an optically...Ch. 31 - Prob. 31.23PCh. 31 - 31.24 Draw the structure of the following...Ch. 31 - Prob. 31.25PCh. 31 - Locate the isoprene units in each compound. a. e....Ch. 31 - 31.27 Classify each terpene and terpenoid in...Ch. 31 - 31.38 Draw the products formed when cholesterol is...Ch. 31 - 31.29 An isoprene unit can be thought of as having...Ch. 31 - 31.30 Draw a stepwise mechanism for the conversion...Ch. 31 - Prob. 31.31PCh. 31 - Prob. 31.32PCh. 31 - Draw three-dimensional structures f or each...Ch. 31 - Prob. 31.34PCh. 31 - Prob. 31.35PCh. 31 - Prob. 31.36PCh. 31 - Prob. 31.37PCh. 31 - 31.38 Draw the products formed when cholesterol is...Ch. 31 - 31.39 Draw a stepwise mechanism for the following...Ch. 31 - 31.40 Draw a stepwise mechanism for the following...Ch. 31 - Prob. 31.41P
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Draw condensed structural formulas for all products obtained from the complete hydrolysis of the following triacylglycerol under acidic conditions.arrow_forwardConsider the compound Hesperetin which belongs to the flavanone class of flavonoids. Hesperetin, in the form of its glycoside hesperidin, is the predominant flavonoid in lemons and oranges. Label any polar bonds in the structure using a crossed arrow to show the direction of polarity. For the carbon atoms highlighted blue give the shape and the expected bond angle based on VSEPR. CH CH Sospe CH CH H₂C. CH3 HO Consider the mologul CH OH C11 CH OHarrow_forwardTrue/ False Lipids are non-polar compounds and are soluble in water Steroids and Prostaglandins are classes of compounds which are not saponifiable Triglycerides are simple lipids and are made up of long chain fatty acids esterified with the trihydroxy groups of glycerol. Waxes are esters of long chain fatty acids with long chain alcohols. Sphingomyelins are a class of saponifiable complex lipids and are made up of sphingosine phosphate and amino alcohols.arrow_forward
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- which molecule is not a natirally occuring fatty acid?arrow_forward25. Which of the following statements regarding the physical properties of triacylglycerol is FALSE? -In general, the melting point of a triacylglycerol increases as the degree of unsaturation increases. -In general, the melting point of a triacylglycerol decreases as the degree of unsaturation increases. -In general, the melting point of a triacylglycerol increases as the number of carbons in the hydrocarbon chain increases. -In general, triacylglycerol with saturated fatty acids are solids are room temperature.arrow_forwardTRANS-fatty acid chains are relatively linear and can pack relatively easily with neighboring fatty acid chains, while CIS-fatty acid chains are relatively crooked and do not pack very easily with neighboring fatty acid chains. True Falsearrow_forward
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