Concept explainers
Interpretation:
The mechanism for the synthesis of fatty
Concept Introduction:
Glycolysis: It is pathway which describes conversion of one molecule of glucose into two molecules of pyruvate. The series involves 10 reactions.
Fatty acid conversion to fatty
Want to see the full answer?
Check out a sample textbook solutionChapter 24 Solutions
Organic Chemistry (8th Edition)
- In the biosynthesis of aromatic amino acids, erythrose-4-phosphate undergoes electrophilic addition to phosphoenolpyruvate (PEP). Draw the products of this step, paying particular attention to regiochemistry. ОН OPOH ОН ? Enzyme Erythrose 4-phosphate Phosphoenolpyruvate (PEP)arrow_forwardIf an enzyme-catalyzed reaction has a high rate at low pH and low rate at higher pH, this implies that a group on either the enzyme or the substrate must be for an efficient reaction. leaving group oxidoreductase coenzymes O protonated deprotonated The compound that consists of deoxyribose linked by an N-glycosidic bond to N-9 of guanine is: adenylate deoxyguanosine guanosine nucleotide guanylatearrow_forwardIdentify the organic functional group and reaction type for the following reaction. The reactant is a(n) - carboxylic acid hexose - Aldohexose - aldotetrose -deoxyhexose -carboxylic acid tetrose - ketohexose The product is a(n) - carboxylic acid tetrose - aldotetrose -alcohol hexose -aldohexose -carboxylic acid hexose - alcohol tetrose The reaction type is - hemiacetal formation -hydrolysis -oxidation( Benedict’s) -acetal formation -reduction( hydrogenation) - mutarotationarrow_forward
- Imidazoleglycerol‑phosphate dehydratase is an enzyme in the histine biosynthesis pathway. It catalyzes the E1 dehydration of D‑erthyro‑imidazole‑glycerol phosphate to imidazole acetol‑phosphate. This is a rare example of a biological E1 reaction, as most biological elimination reactions occur through E1cB instead. In this reaction, D‑erthyro‑imidazole‑glycerol phosphate is first protonated to form a good leaving group. Then, the leaving group is ejected to form the resonance‑stabilized carbocation shown. Draw curved arrows forming the most stable resonance structure to explain why this reaction goes through an E1 mechanism. Draw curved arrows to form the most stable resonance structure.arrow_forwardPredict the product(s) obtained when each of the following compounds is treated with a mixture of nitric acid and sulfuric acid. Select all that apply. 18.41d * Your answer is incorrect.arrow_forwardThe vitamin Niacin is used to form nicotinamide adenosine dinucleotide, which readily shuttles between its oxidized (NAD+) and reduced (NADH) forms. The latter serves as a cellular equivalent to NaBH4. The essential portions of the structures are shown below. Outline a mechanism for the cellular conversion of pyruvate to lactate. (Note: like NaBH4, NADH cannot reduce carboxylic acid carbonyls).arrow_forward
- The hydrolysis of an ester can be sped up by both acidic and basic conditions. Aminolysis of an ester can be sped up by acidic conditions, but not by basic conditions. Explain why.arrow_forwardName the enzyme that will catalyze the following reaction of ethanol oxidation to acetaldehyde (ethanal). CH3-CH₂-OH + NAD* → CH3-CHO + NADH + H* O alcohol dehydrogenase alcohol hydrolase alcohol isomerase O alcohol transferasearrow_forwardNonearrow_forward
- 5. Oxidation and Reduction Reactions - Product Prediction of the following reactions. OH OEt NADP+ NADPH Draw the organic productsarrow_forwardAcetolactate synthase transfers the acyl group of pyruvate to alpha-ketobutyrate. This is the first step in the biosynthesis of the amino acid isoleucine. Propose a mechanism for this reaction.arrow_forwardThe same E1–E2–E3 multienzyme structure found in the pyruvate dehydrogenase and the a-ketoglutarate dehydrogenase complexes is also used in the branched-chain a-ketoacid dehydrogenase complex, which participates in the catabolism of branched-chain amino acids. Draw the reaction product when the following substrate is acted on by the branched-chain a-keto acid dehydrogenase complex.arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,