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Concept explainers
(a)
Interpretation:
The fatty acids that are used to form the given triacylglycerol should be determined.
Concept Introduction:
Triacylglycerols are esters that are formed by reacting three molecules of fatty acids with one molecule of glycerol. If all the three fatty acids are identical it is called a simple triacylglycerol and if there are two or more different fatty acids, it is called a mixed triacylglycerol. Depending on whether the fatty acids involved are saturated or unsaturated, there are two types of triacylglycerols.
(b)
Interpretation:
Whether the triacylglycerol is expected to be a solid or a liquid at room temperature should be determined.
Concept Introduction:
Triacylglycerols are esters that are formed by reacting three molecules of fatty acids with one molecule of glycerol. If all the three fatty acids are identical it is called a simple triacylglycerol and if there are two or more different fatty acids, it is called a mixed triacylglycerol. Depending on whether the fatty acids involved are saturated or unsaturated, there are two types of triacylglycerols.
(c)
Interpretation:
Hydrophobic regions in the triacylglycerol should be labeled.
Concept Introduction:
Triacylglycerols are esters that are formed by reacting three molecules of fatty acids with one molecule of glycerol. If all the three fatty acids are identical it is called a simple triacylglycerol and if there are two or more different fatty acids, it is called a mixed triacylglycerol. Depending on whether the fatty acids involved are saturated or unsaturated, there are two types of triacylglycerols.
(d)
Interpretation:
Hydrophilic regions in the triacylglycerol should be labeled.
Concept Introduction:
Triacylglycerols are esters that are formed by reacting three molecules of fatty acids with one molecule of glycerol. If all the three fatty acids are identical it is called a simple triacylglycerol and if there are two or more different fatty acids, it is called a mixed triacylglycerol. Depending on whether the fatty acids involved are saturated or unsaturated, there are two types of triacylglycerols.
(e)
Interpretation:
Hydrolysis products that are formed when the triacylglycerol is treated with aqueous sulfuric acid should be determined.
Concept Introduction:
Triacylglycerols are esters that are formed by reacting three molecules of fatty acids with one molecule of glycerol. If all the three fatty acids are identical it is called a simple triacylglycerol and if there are two or more different fatty acids, it is called a mixed triacylglycerol. Depending on whether the fatty acids involved are saturated or unsaturated, there are two types of triacylglycerols.
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Chapter 19 Solutions
EBK GENERAL, ORGANIC, & BIOLOGICAL CHEM
- Q1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label each compound as chiral or achiral. OH HO CI Br H CI CI Br CI CI Xf x f g Br D OH Br Br H₂N R. IN Ill I -N S OMe D II H CO₂H 1/111 DuckDuckGarrow_forwardThese are synthesis questions. You need to show how the starting material can be converted into the product(s) shown. You may use any reactions we have learned. Show all the reagents you need. Show each molecule synthesized along the way and be sure to pay attention to the regiochemistry and stereochemistry preferences for each reaction. If a racemic molecule is made along the way, you need to draw both enantiomers and label the mixture as "racemic". All of the carbon atoms of the products must come from the starting material! ? H Harrow_forwardQ5: Draw every stereoisomer for 1-bromo-2-chloro-1,2-difluorocyclopentane. Clearly show stereochemistry by drawing the wedge-and-dashed bonds. Describe the relationship between each pair of the stereoisomers you have drawn.arrow_forward
- Classify each pair of molecules according to whether or not they can participate in hydrogen bonding with one another. Participate in hydrogen bonding CH3COCH3 and CH3COCH2CH3 H2O and (CH3CH2)2CO CH3COCH3 and CH₂ CHO Answer Bank Do not participate in hydrogen bonding CH3CH2OH and HCHO CH3COCH2CH3 and CH3OHarrow_forwardNonearrow_forwardQ4: Comparing (3S,4S)-3,4-dimethylhexane and (3R,4S)-3,4-dimethylhexane, which one is optically active? Briefly explain.arrow_forward
- Nonearrow_forwardNonearrow_forwardGiven the standard enthalpies of formation for the following substances, determine the reaction enthalpy for the following reaction. 4A (g) + 2B (g) → 2C (g) + 7D (g) AHrxn =?kJ Substance AH in kJ/mol A (g) - 20.42 B (g) + 32.18 C (g) - 72.51 D (g) - 17.87arrow_forward
- Determine ASran for Zn(s) + 2HCl(aq) = ZnCl2(aq) + H2(aq) given the following information: Standard Entropy Values of Various Substance Substance So (J/mol • K) 60.9 Zn(s) HCl(aq) 56.5 130.58 H2(g) Zn2+(aq) -106.5 55.10 CI (aq)arrow_forward3) Catalytic hydrogenation of the compound below produced the expected product. However, a byproduct with molecular formula C10H12O is also formed in small quantities. What is the by product?arrow_forwardWhat is the ΔHorxn of the reaction? NaOH(aq) + HCl(aq) → H2O(l) + NaCl(aq) ΔHorxn 1= ________ kJ/molarrow_forward
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
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