![Bundle: General, Organic, and Biological Chemistry, 7th + OWLv2 Quick Prep for General Chemistry, 4 terms (24 months) Printed Access Card](https://www.bartleby.com/isbn_cover_images/9781305717534/9781305717534_largeCoverImage.gif)
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.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 25 Solutions
Bundle: General, Organic, and Biological Chemistry, 7th + OWLv2 Quick Prep for General Chemistry, 4 terms (24 months) Printed Access Card
- टे Predict the major products of this organic reaction. Be sure to use wedge and dash bonds when necessary, for example to distinguish between different major products. ☐ ☐ : ☐ + NaOH HO 2 Click and drag to start drawing a structure.arrow_forwardShown below are five NMR spectra for five different C6H10O2 compounds. For each spectrum, draw the structure of the compound, and assign the spectrum by labeling H's in your structure (or in a second drawing of the structure) with the chemical shifts of the corresponding signals (which can be estimated to nearest 0.1 ppm). IR information is also provided. As a reminder, a peak near 1700 cm-1 is consistent with the presence of a carbonyl (C=O), and a peak near 3300 cm-1 is consistent with the presence of an O–H. Extra information: For C6H10O2 , there must be either 2 double bonds, or 1 triple bond, or two rings to account for the unsaturation. There is no two rings for this problem. A strong band was observed in the IR at 1717 cm-1arrow_forwardPredict the major products of the organic reaction below. : ☐ + Х ك OH 1. NaH 2. CH₂Br Click and drag to start drawing a structure.arrow_forward
- NG NC 15Show all the steps you would use to synthesize the following products shown below using benzene and any organic reagent 4 carbons or less as your starting material in addition to any inorganic reagents that you have learned. NO 2 NC SO3H NO2 OHarrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forwardShow work...don't give Ai generated solutionarrow_forward
- 1 Please provide an efficient synthesis of the product below from the starting material. Use the starting material as the ONLY source of carbon atoms. Show the synthesis of each compound that would be used in the overall synthesis of the product. [This synthesis uses alkyne and alcohol chemistry.]arrow_forward10- 4000 20 20 30- %Reflectance 60 50- 09 60- 40- Date: Thu Feb 06 17:30:02 2025 (GMT-05:0(UnknownP Scans: 8 Resolution: 2.000 70 70 88 80 3500 3000 2500 90 100 00 Wavenumbers (cm-1) 2000 1500 2983.10 2359.13 1602.52 1584.22 1451.19 1391.87 1367.07 1314.37 1174.34 1070.13 1027.33 1714.16 1269.47 1000 1106.08 1001.14 937.02 873.60 850.20 780.22 686.91 674.38 643.09 617.98 02/06/25 16:38:20arrow_forwardd. Draw arrow-pushing mechanism for an enzymatic retro-aldol reaction of the following hexose. Use B: and/or HA as needed. OH OH سية HO OH OHarrow_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,
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305960060/9781305960060_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781285853918/9781285853918_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305081079/9781305081079_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781337399692/9781337399692_smallCoverImage.gif)