![General, Organic, and Biological Chemistry: Structures of Life (5th Edition)](https://www.bartleby.com/isbn_cover_images/9780321967466/9780321967466_largeCoverImage.gif)
Concept explainers
(a)
To determine: The line–angle structural formula for the activated form of lauric acid.
![Check Mark](/static/check-mark.png)
Answer to Problem 24.71UTC
Solution: The line–angle structural formula for the activated form of lauric acid is:
Explanation of Solution
Lauric acid is a saturated fatty acid. It can be activated by Coenzyme A catalysed by Acyl CoA synthetase.
Thus, the activated form of Lauric acid is:
(b)
To determine: The α- and β-carbon atoms in the acyl molecule of lauric acid.
![Check Mark](/static/check-mark.png)
Answer to Problem 24.71UTC
Solution: The α- and β-carbon atoms in the acyl molecule of lauric acid is:
Explanation of Solution
The carbon attached to the carbonyl carbon is considered as α-carbon and the carbon next to α-carbon is called as β-carbon.
Thus the α- and β-carbon atoms in the acyl molecule of lauric acid can be represented as
(c)
To determine: The number of cycles of β- oxidation needed for complete β-oxidation of lauric acid.
![Check Mark](/static/check-mark.png)
Answer to Problem 24.71UTC
Solution: The number of cycles of β- oxidation needed for complete β-oxidation of lauric acid is five ().
Explanation of Solution
The acetyl group of the acetyl CoA is formed by two carbons and in the last round two acetyl CoA is produced. Accordingly the number of cycles of β-oxidation has been calculated.
No. of cycles of β-oxidation are needed for the complete oxidation of fatty acid = (n/2)-1 where n = No. of carbon atoms present in fatty acid.
As here no. of carbon atoms in the given fatty acid = 12
So, by putting n = 12
We get, No. of cycles of β-oxidation are needed for the complete oxidation of fatty acid = (12/2) -1 = 5
Thus, five () cycles of β-oxidation are needed for the complete oxidation of lauric acid.
(d)
To determine: The number of acetyl CoA units produced from the complete β-oxidation of lauric acid.
![Check Mark](/static/check-mark.png)
Answer to Problem 24.71UTC
Solution: The number of acetyl CoA units produced from the complete β-oxidation of lauric acid is six ().
Explanation of Solution
The acetyl group of the acetyl CoA is formed by two carbons. Accordingly the number of acetyl CoA produced has been calculated.
No. of acetyl CoA are produced from the complete oxidation of fatty acid = (n/2)
where n = No. of carbon atoms present in fatty acid.
As here no. of carbon atoms in the given fatty acid = 12
So, by putting n=12
We get, No. of acetyl CoA are produced from the complete oxidation of fatty acid = (12/2) = 6
Thus, from complete oxidation of lauric acid six(6) acetyl CoA are produced.
(e)
To determine: The total ATP yield from the complete β-oxidation of lauric acid.
![Check Mark](/static/check-mark.png)
Answer to Problem 24.71UTC
Solution: The total ATP yield from the complete β-oxidation of lauric acid is .
Explanation of Solution
From the complete β-oxidation of lauric acid, total six(6) acetyl CoA, 5 NADH and 6 FADH2 has been produced. Each Acetyl CoA yields 10 ATP, each NADH yields 2.5 ATP and each FADH2 yields 1.5 ATP. Accordingly, ATP yield has been calculated.
Lauric Acid is a C12 fatty acid. And for the activation of lauric acid 2 ATP is required.
Activation | -2 ATP | |
Acetyl CoA | 6x10ATP/Acetyl CoA | 60ATP |
NADH.H | 5x2.5 ATP/NADH | 12.5 ATP |
FADH2 | 5x1.5 ATP/ FADH2 | 7.5 ATP |
Total | 78 ATP |
Thus, 78 ATP yields from the complete oxidation of lauric acid.
Therefore, the line-angle structural formula for the activated form, α- and β-carbon atoms in the acyl molecule, number of cycles of β- oxidation, number of acetyl CoA units produced and the total ATP yield from the complete β- oxidation of lauric acid has been discussed.
Want to see more full solutions like this?
Chapter 24 Solutions
General, Organic, and Biological Chemistry: Structures of Life (5th Edition)
- Nonearrow_forwardTransmitance 3. Which one of the following compounds corresponds to this IR spectrum? Point out the absorption band(s) that helped you decide. OH H3C OH H₂C CH3 H3C CH3 H3C INFRARED SPECTRUM 0.8- 0.6 0.4- 0.2 3000 2000 1000 Wavenumber (cm-1) 4. Consider this compound: H3C On the structure above, label the different types of H's as A, B, C, etc. In table form, list the labeled signals, and for each one state the number of hydrogens, their shifts, and the splitting you would observe for these hydrogens in the ¹H NMR spectrum. Label # of hydrogens splitting Shift (2)arrow_forwardNonearrow_forward
- Draw the Lewis structure of C2H4Oarrow_forwarda) 5. Circle all acidic (and anticoplanar to the Leaving group) protons in the following molecules, Solve these elimination reactions, and identify the major and minor products where appropriate: 20 points + NaOCH3 Br (2 productarrow_forwardNonearrow_forward
- Dr. Mendel asked his BIOL 260 class what their height was and what their parent's heights were. He plotted that data in the graph below to determine if height was a heritable trait. A. Is height a heritable trait? If yes, what is the heritability value? (2 pts) B. If the phenotypic variation is 30, what is the variation due to additive alleles? (2 pts) Offspring Height (Inches) 75 67.5 60 52.5 y = 0.9264x + 4.8519 55 60 65 MidParent Height (Inches) 70 75 12pt v V Paragraph B IUA > AT2 v Varrow_forwardExperiment: Each team will be provided with 5g of a mixture of acetanilide and salicylic acid. You will divide it into three 1.5 g portions in separate 125 mL Erlenmeyer flasks savıng some for melting point analysis. Dissolve the mixture in each flask in ~60mL of DI water by heating to boiling on a hotplate. Take the flasks off the hotplate once you have a clear solution and let them stand on the bench top for 5 mins and then allow them to cool as described below. Sample A-Let the first sample cool slowly to room temperature by letting it stand on your lab bench, with occasional stirring to promote crystallization. Sample B-Cool the second sample 1n a tap-water bath to 10-15 °C Sample C-Cool the third sample in an ice-bath to 0-2 °C Results: weight after recrystalization and melting point temp. A=0.624g,102-115° B=0.765g, 80-105° C=1.135g, 77-108 What is the percent yield of A,B, and C.arrow_forwardRel. Intensity Q 1. Which one of the following is true of the compound whose mass spectrum is shown here? Explain how you decided. 100 a) It contains chlorine. b) It contains bromine. c) It contains neither chlorine nor bromine. 80- 60- 40- 20- 0.0 0.0 TT 40 80 120 160 m/z 2. Using the Table of IR Absorptions how could you distinguish between these two compounds in the IR? What absorbance would one compound have that the other compound does not? HO CIarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)