
Concept explainers
(a)
Interpretation:
HMG-CoA is encountered in the process (1) glycerol
Concept introduction:
Lipogenesis is the process employed for the synthesis of fatty acid. The starting precursor for the synthesis is acetyl CoA. The enzyme employed for the process is fatty acid synthase. It is a multienzyme complex that ties the reaction responsible for the synthesis of fatty acid. The fatty acid is synthesized in two parts. In the first part, there is citrate-malate shuttle system and in the second part, there is a cyclic process to synthesize saturated fatty acid.
The fatty acids are broken down to provide energy. The breakdown of fatty acids is a three parts process. In the first part, the fatty acid is activated. In the second part, the transportation of fatty acid into the mitochondrial matrix is facilitated by a shuttle mechanism. In the third part, the fatty acid is readily oxidized, cycling through a series of four reactions. In these series of reactions, acyl CoA is degraded to acetyl CoA. This pathway is termed as β-oxidation pathway.
Ketogenesis is a metabolic process by which
Triacylglycerol mobilization is an ongoing process in which triacylglycerols that are stored in the adipose tissue are hydrolyzed. Fatty acids and glycerol are the products of triacylglycerol mobilization. The products are released into the bloodstream.
After entering the bloodstream, the glycerol travels to the kidneys or liver. The first stage of glycerol metabolism occurs in the liver or kidney where it is converted to
(a)

Answer to Problem 14.104EP
HMG-CoA is encountered in ketogenesis.
Explanation of Solution
HMG-CoA is produced in step 2 in ketogenesis.
Step 2 is a condensation reaction. In step 2, acetoacetyl CoA reacts with acetyl CoA and water to produce 3-hydroxyl-3-methylglutaryl (HMG-CoA) and CoA-SH. The reaction for step 2 is:
(b)
Interpretation:
NADPH is encountered in the process (1) glycerol metabolism to dihydroxyacetone phosphate, (2) β-oxidation pathway, (3) ketogenesis, and (4) lipogenesis has to be identified.
Concept introduction:
Lipogenesis is the process employed for the synthesis of fatty acid. The starting precursor for the synthesis is acetyl CoA. The enzyme employed for the process is fatty acid synthase. It is a multienzyme complex that ties the reaction responsible for the synthesis of fatty acid. The fatty acid is synthesized in two parts. In the first part, there is citrate-malate shuttle system and in the second part, there is a cyclic process to synthesize saturated fatty acid.
The fatty acids are broken down to provide energy. The breakdown of fatty acids is a three parts process. In the first part, the fatty acid is activated. In the second part, the transportation of fatty acid into the mitochondrial matrix is facilitated by a shuttle mechanism. In the third part, the fatty acid is readily oxidized, cycling through a series of four reactions. In these series of reactions, acyl CoA is degraded to acetyl CoA. This pathway is termed as β-oxidation pathway.
Ketogenesis is a metabolic process by which ketone bodies are produced by the breakdown of fatty acids and ketogenic amino acids. This metabolic process supplies our organs with needed energy under certain circumstances such as starvation. Fatty acid molecules degrade into acetyl CoA which are utilized as reactants in the process of ketogenesis. These molecules of acetyl CoA undergo the process of condensation twice, followed by chain cleavage and hydrogenation to produce ketone bodies.
Triacylglycerol mobilization is an ongoing process in which triacylglycerols that are stored in the adipose tissue are hydrolyzed. Fatty acids and glycerol are the products of triacylglycerol mobilization. The products are released into the bloodstream.
After entering the bloodstream, the glycerol travels to the kidneys or liver. The first stage of glycerol metabolism occurs in the liver or kidney where it is converted to
(b)

Answer to Problem 14.104EP
NADPH is encountered in lipogenesis.
Explanation of Solution
NADPH acts as the reducing agent in step 2 and 4 of the cyclic process of lipogenesis. NADPH gets oxidized to form NADP+.
Step 2 involves the hydrogenation of acetoacetyl ACP to synthesis β-hydroxybutyrylwith the help of reducing agent NADPH. The reaction of this step is:
Step 4 again involves hydrogenation reaction. In this step, crotonyl ACP is converted to butyryl ACP with the help of reducing agent NADPH. The reaction of this step is:
(c)
Interpretation:
Malonyl ACP is encountered in the process (1) glycerol metabolism to dihydroxyacetone phosphate, (2) β-oxidation pathway, (3) ketogenesis, and (4) lipogenesis has to be identified.
Concept introduction:
Lipogenesis is the process employed for the synthesis of fatty acid. The starting precursor for the synthesis is acetyl CoA. The enzyme employed for the process is fatty acid synthase. It is a multienzyme complex that ties the reaction responsible for the synthesis of fatty acid. The fatty acid is synthesized in two parts. In the first part, there is citrate-malate shuttle system and in the second part, there is a cyclic process to synthesize saturated fatty acid.
The fatty acids are broken down to provide energy. The breakdown of fatty acids is a three parts process. In the first part, the fatty acid is activated. In the second part, the transportation of fatty acid into the mitochondrial matrix is facilitated by a shuttle mechanism. In the third part, the fatty acid is readily oxidized, cycling through a series of four reactions. In these series of reactions, acyl CoA is degraded to acetyl CoA. This pathway is termed as β-oxidation pathway.
Ketogenesis is a metabolic process by which ketone bodies are produced by the breakdown of fatty acids and ketogenic amino acids. This metabolic process supplies our organs with needed energy under certain circumstances such as starvation. Fatty acid molecules degrade into acetyl CoA which are utilized as reactants in the process of ketogenesis. These molecules of acetyl CoA undergo the process of condensation twice, followed by chain cleavage and hydrogenation to produce ketone bodies.
Triacylglycerol mobilization is an ongoing process in which triacylglycerols that are stored in the adipose tissue are hydrolyzed. Fatty acids and glycerol are the products of triacylglycerol mobilization. The products are released into the bloodstream.
After entering the bloodstream, the glycerol travels to the kidneys or liver. The first stage of glycerol metabolism occurs in the liver or kidney where it is converted to
(c)

Answer to Problem 14.104EP
Malonyl ACP is encountered in lipogenesis.
Explanation of Solution
Malonyl ACP is the reactant in step 1 in the cyclic process in lipogenesis.
The first step involves the condensation reaction between acetyl ACP and malonyl ACP. The product formed in the first reaction is acetoacetyl ACP. The reaction of step 1 is:
(d)
Interpretation:
Acetoacetyl CoA is encountered in the process (1) glycerol metabolism to dihydroxyacetone phosphate, (2) β-oxidation pathway, (3) ketogenesis, and (4) lipogenesis has to be identified.
Concept introduction:
Lipogenesis is the process employed for the synthesis of fatty acid. The starting precursor for the synthesis is acetyl CoA. The enzyme employed for the process is fatty acid synthase. It is a multienzyme complex that ties the reaction responsible for the synthesis of fatty acid. The fatty acid is synthesized in two parts. In the first part, there is citrate-malate shuttle system and in the second part, there is a cyclic process to synthesize saturated fatty acid.
The fatty acids are broken down to provide energy. The breakdown of fatty acids is a three parts process. In the first part, the fatty acid is activated. In the second part, the transportation of fatty acid into the mitochondrial matrix is facilitated by a shuttle mechanism. In the third part, the fatty acid is readily oxidized, cycling through a series of four reactions. In these series of reactions, acyl CoA is degraded to acetyl CoA. This pathway is termed as β-oxidation pathway.
Ketogenesis is a metabolic process by which ketone bodies are produced by the breakdown of fatty acids and ketogenic amino acids. This metabolic process supplies our organs with needed energy under certain circumstances such as starvation. Fatty acid molecules degrade into acetyl CoA which are utilized as reactants in the process of ketogenesis. These molecules of acetyl CoA undergo the process of condensation twice, followed by chain cleavage and hydrogenation to produce ketone bodies.
Triacylglycerol mobilization is an ongoing process in which triacylglycerols that are stored in the adipose tissue are hydrolyzed. Fatty acids and glycerol are the products of triacylglycerol mobilization. The products are released into the bloodstream.
After entering the bloodstream, the glycerol travels to the kidneys or liver. The first stage of glycerol metabolism occurs in the liver or kidney where it is converted to
(d)

Answer to Problem 14.104EP
Acetoacetyl CoA is encountered in ketogenesis.
Explanation of Solution
Step 2 is a condensation reaction. In step 2, acetoacetyl CoA reacts with acetyl CoA and water to produce 3-hydroxyl-3-methylglutaryl (HMG-CoA) and CoA-SH. The reaction for step 2 is:
Want to see more full solutions like this?
Chapter 14 Solutions
Organic And Biological Chemistry
- 151.2 254.8 85.9 199.6 241.4 87.6 242.5 186.4 155.8 257.1 242.9 253.3 256.0 216.6 108.7 239.0 149.7 236.4 152.1 222.7 148.7 278.2 268.7 234.4 262.7 283.2 143.6 QUESTION: Using this group of data on salt reduced tomato sauce concentration readings answer the following questions: 1. 95% Cl Confidence Interval (mmol/L) 2. [Na+] (mg/100 mL) 3. 95% Na+ Confidence Interval (mg/100 mL)arrow_forwardResults Search Results Best Free Coursehero Unloc xb Success Confirmation of Q x O Google Pas alekscgi/x/lsl.exe/1o_u-IgNslkr 7j8P3jH-IQs_pBanHhvlTCeeBZbufu BYTI0Hz7m7D3ZcHYUt80XL-5alyVpwDXM TEZayFYCavJ17dZtpxbFD0Qggd1J O States of Matter Using a phase diagram to find a phase transition temperature or pressure Gabr 3/5 he pressure above a pure sample of solid Substance X at 101. °C is lowered. At what pressure will the sample sublime? Use the phase diagram of X below to nd your answer. pressure (atm) 24- 12 solid liquid gas 200 400 temperature (K) 600 ote: your answer must be within 0.15 atm of the exact answer to be graded correct. atm Thanation Check © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center I Q Search L³ ملةarrow_forward301.7 348.9 193.7 308.6 339.5 160.6 337.7 464.7 223.5 370.5 326.6 327.5 336.1 317.9 203.8 329.8 221.9 331.7 211.7 309.6 223.4 353.7 334.6 305.6 340.0 304.3 244.7 QUESTION: Using this group of data on regular tomato sauce concentration readings answer the following questions: 1. 95% Cl Confidence Interval (mmol/L) 2. [Na+] (mg/100 mL) 3. 95% Na+ Confidence Interval (mg/100 mL)arrow_forward
- Search Results Search Results Best Free Coursehero Unlo x b Success Confirmation of Q aleks.com/alekscgi/x/sl.exe/10_u-lgNslkr7j8P3jH-IQs_pBan HhvlTCeeBZbufu BYTIOHz7m7D3ZcHYUt80XL-5alyVpwDXM TEZayFYCav States of Matter Using a phase diagram to find a phase transition temperature or pressure Use the phase diagram of Substance X below to find the temperature at which X turns to a gas, if the pressure above the solid is 3.7 atm. pressure (atm) 0. 32- 16 solid liquid gas 200 temperature (K) Note: your answer must be within 20 °C of the exact answer to be graded correct. Дос Xarrow_forwardConsider the reaction below to answer the following questions: Acetoacetic ester can be prepared by the Claisen self-condensation reaction of ethyl acetate. 1. NaOEt, EtOH H&C OCH CH3 2 H30 H3C CH2 OCH2CH3 A. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and draw all intermediate structures. B. Ethyl acetate can be prepared from ethanol as the only organic starting material. Show all reagents and structures for all intermediates in this preparation. C. Give the structures of the ester precursors for the following Claisen condensation product and formulate the reaction. OEtarrow_forwardUse the phase diagram of Substance X below to find the temperature at which X turns to a gas, if the pressure above the solid is 3.7 atm. pressure (atm) 32 16 solid liquid gas 0 0 200 temperature (K) Note: your answer must be within 20 °C of the exact answer to be graded correct. Шос ☑ كarrow_forward
- Starting from bromoethane, how could you prepare the following compounds: a. Ethanol. b. Acetaldehyde f. Acetone. e. 2-Propanol i. Acetoacetic ester. d. 2-Bromoacetic acid. c. Acetic acid g. Acetamide. j. Ethylmalonate k. Gama ketoacid. h. Ethyl magnesium bromide.arrow_forward- The pressure above a pure sample of solid Substance X at 60. °C is raised. At what pressure will the sample melt? Use the phase diagram of X below to find your answer. pressure (atm) 02 0.4 solid Hliquid gas 0 0 200 400 600 temperature (K) Note: your answer must be within 0.025 atm of the exact answer to be graded correct. ☐ atmarrow_forward15. What is the order of decreasing reactivity towards nucleophilic acyl substitution for the carboxylic acid derivatives? (most reactive first) 0 O H3C COC CH3 H₂C C N(CH3)2 H3C C OCH3 A. a. I, 11, 111, b. I, III, IV, II C. II, IV, III, I ° (CH3)2CH C OCH3 IV d. II, I, III, IV B. R COCR 0 0 0 13= RC NH2 RC OR RC CI === IV a. I, III, II, IV b. II, III, I, IV C. III, II, I, IV d. IV, I, III, IIarrow_forward
- Draw the formula of the product obtained by reacting D-Tallose with bromine water.arrow_forwardChoose the best reagent(s) for carrying out the following conversions from the list below. Place the letter corresponding to the best choice in the blank to the left of the conversion. a. KMnO4, H3O+ b. Tollens' Reagent [oxidizing reagent] C. NaBH4, ethanol d. 1. BH3 2. H3O+ e. 1. CH3MgBr, ether 2. H3O+ f. CrO3, H2SO4, H₂O g. 1. Mg, ether 2. CO2 3. H3O+ h. 1. NaCN 2. H2SO4, H2, heat i. O3, then Zn and HOAC j. CH₂I A. B. C. CH CH=CHCH2COOH Br CEN CH COOH + HOOCCH COOH COOH 010 CH3arrow_forwardDraw the structures for each of the intermediates in the boxes provided for the synthesis below. OCH3 Fe HO HNO (CHOO pynding H₂504 LHNO2 NACH-I Fa H₂O HCL HNO 180arrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningGeneral, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning



