Concept explainers
(a)
Interpretation:
The following intermediate compound generated in the first or second cycle of the lipogenesis pathway is produced by (1) a dehydration reaction, (2) a hydrogenation reaction, or (3) a condensation reaction 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 different reactions that are involved in the cyclic process are:
In hydrogenation reaction, a hydrogen molecule (H2) is added to an organic substance; in hydration reaction, a water molecule (H2O) is added to an unsaturated substrate; in the condensation reaction, two molecules combine to form a single product.
The first turn of the cyclic process produces four-carbon acyl group and the further turns add two carbon unit to the four-carbon acyl group. Therefore, the first turn has four carbon units and the second turn has six carbon unit in their intermediate compound.
(b)
Interpretation:
The following intermediate compound generated in the first or second cycle of the lipogenesis pathway is produced by (1) a dehydration reaction, (2) a hydrogenation reaction, or (3) a condensation reaction 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 different reactions that are involved in the cyclic process are:
In hydrogenation reaction, a hydrogen molecule (H2) is added to an organic substance; in hydration reaction, a water molecule (H2O) is added to an unsaturated substrate; in the condensation reaction, two molecules combine to form a single product.
The first turn of the cyclic process produces four-carbon acyl group and the further turns add two carbon unit to the four-carbon acyl group. Therefore, the first turn has four carbon units and the second turn has six carbon unit in their intermediate compound.
(c)
Interpretation:
The following intermediate compound generated in the first or second cycle of the lipogenesis pathway is produced by (1) a dehydration reaction, (2) a hydrogenation reaction, or (3) a condensation reaction 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 different reactions that are involved in the cyclic process are:
In hydrogenation reaction, a hydrogen molecule (H2) is added to an organic substance; in hydration reaction, a water molecule (H2O) is added to an unsaturated substrate; in the condensation reaction, two molecules combine to form a single product.
The first turn of the cyclic process produces four-carbon acyl group and the further turns add two carbon unit to the four-carbon acyl group. Therefore, the first turn has four carbon units and the second turn has six carbon unit in their intermediate compound.
(d)
Interpretation:
The following intermediate compound generated in the first or second cycle of the lipogenesis pathway is produced by (1) a dehydration reaction, (2) a hydrogenation reaction, or (3) a condensation reaction 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 different reactions that are involved in the cyclic process are:
In hydrogenation reaction, a hydrogen molecule (H2) is added to an organic substance; in hydration reaction, a water molecule (H2O) is added to an unsaturated substrate; in the condensation reaction, two molecules combine to form a single product.
The first turn of the cyclic process produces four-carbon acyl group and the further turns add two carbon unit to the four-carbon acyl group. Therefore, the first turn has four carbon units and the second turn has six carbon unit in their intermediate compound.

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Chapter 14 Solutions
EBK ORGANIC AND BIOLOGICAL CHEMISTRY
- Draw the most stable cations formed in the mass spectrometer by a deavage of the following compound Draw the most stable cations formed in the mass spectrometer by a cleavage of the following compound онarrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting anand product sytucutrs, draw the curved electron-pusing arrows for the following reaction or mechanistic steps. Be sure to account for all bond-breaking and bind-making stepsarrow_forwardDraw the major elimination and substitution products formed in this reavtion. Use a dash or wedge bond to indicatr the stereochemistry of substituents on assymetric centers, wheere applicable. Ignore any inorganic byproducts.arrow_forward
- Draw the two possible products produced in this E2 elimination. Ignore any inorganic byproductsarrow_forwardDraw the major products of this SN1 reaction. Ignore any inorganic byproducts.arrow_forwardDraw the major elimination and substitution products formed in this reaction. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, wehre applicable. Ignore and inorganic byproducts.arrow_forward
- Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Drawing Arrows THE Problem 33 of 35 N. C:0 Na + Submit Drag To Pan +arrow_forwardDraw the product of the E2 reaction shown below. Include the correct stereochemistry. Ignore and inorganic byproducts.arrow_forwardDraw the major producrs of this SN1 reaction. Ignore any inorganic byproducts. Use a dash or wedge bond to indicate the sereochemistry of substituents on asymmetric centers where appllicable.arrow_forward
- 5) Oxaloacetic Acid is an important intermediate in the biosynthesis of citric acid. Synthesize oxaloacetic acid using a mixed Claisen Condensation reaction with two different esters and a sodium ethoxide base. Give your answer as a scheme Hint 1: Your final acid product is producing using a decarboxylation reaction. Hint 2: Look up the structure of oxalic acid. HO all OH oxaloacetic acidarrow_forward20. The Brusselator. This hypothetical system was first proposed by a group work- ing in Brussels [see Prigogine and Lefever (1968)] in connection with spatially nonuniform chemical patterns. Because certain steps involve trimolecular reac tions, it is not a model of any real chemical system but rather a prototype that has been studied extensively. The reaction steps are A-X. B+X-Y+D. 2X+ Y-3X, X-E. 305 It is assumed that concentrations of A, B, D, and E are kept artificially con stant so that only X and Y vary with time. (a) Show that if all rate constants are chosen appropriately, the equations de scribing a Brusselator are: dt A-(B+ 1)x + x²y, dy =Bx-x²y. diarrow_forwardProblem 3. Provide a mechanism for the following transformation: H₂SO A Me. Me Me Me Mearrow_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,



