Concept explainers
(a)
Interpretation:
Electron transport chain occurs within mitochondria of a cell or in a cell’s cytosol has to be indicated.
Concept introduction:
Electron transfer chain is defined as a series of biochemical reactions in which the electrons and hydrogen ions obtained from NADH and FADH2 react with molecular oxygen to produce water. NADH and FADH2 are oxidized through
(b)
Interpretation:
Lipogenesis occurs within mitochondria of a cell or in a cell’s cytosol has to be indicated.
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. This process is the reverse of the degradation of fatty acid.
(c)
Interpretation:
Glycerol
Concept introduction:
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)
Interpretation:
Gluconeogenesis occurs within mitochondria of a cell or in a cell’s cytosol has to be indicated.
Concept introduction:
Gluconeogenesis is an eleven-step pathway in which glucose is produced from non-carbohydrate substances. The net overall equation for gluconeogenesis is as follows:

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Chapter 14 Solutions
EBK ORGANIC AND BIOLOGICAL CHEMISTRY
- Synthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Indicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forward
- Indicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forward
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- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning




