
Concept explainers
(a)
Interpretation: To identify whether citrulline is encountered in the (1) urea cycle, (2) heme degradation process, or (3) oxidative deamination reaction.
Concept introduction: A urea cycle is a cyclic biochemical pathway that involves the production of urea using ammonium ions and aspartate molecules as nitrogen sources. The desired product of the urea cycle is urea.
Heme potion of hemoglobin undergoes a stepwise degradation to biliverdin, to bilirubin, and then to bile pigments that are excreted from the body.
A biochemical reaction in which an
(b)
Interpretation: To identify whether glutamate is encountered in the (1) urea cycle, (2) heme degradation process, or (3) oxidative deamination reaction.
Concept introduction: A urea cycle is a cyclic biochemical pathway that involves the production of urea using ammonium ions and aspartate molecules as nitrogen sources. The desired product of the urea cycle is urea.
Heme potion of hemoglobin undergoes a stepwise degradation to biliverdin, to bilirubin, and then to bile pigments that are excreted from the body.
A biochemical reaction in which an
(c)
Interpretation: To identify whether bilirubin is encountered in the (1) urea cycle, (2) heme degradation process, or (3) oxidative deamination reaction.
Concept introduction: A urea cycle is a cyclic biochemical pathway that involves the production of urea using ammonium ions and aspartate molecules as nitrogen sources. The desired product of the urea cycle is urea.
Heme potion of hemoglobin undergoes a stepwise degradation to biliverdin, to bilirubin, and then to bile pigments that are excreted from the body.
A biochemical reaction in which an
(d)
Interpretation: To identify whether ammonium ion is encountered in the (1) urea cycle, (2) heme degradation process, or (3) oxidative deamination reaction.
Concept introduction: A urea cycle is a cyclic biochemical pathway that involves the production of urea using ammonium ions and aspartate molecules as nitrogen sources. The desired product of the urea cycle is urea.
Heme potion of hemoglobin undergoes a stepwise degradation to biliverdin, to bilirubin, and then to bile pigments that are excreted from the body.
A biochemical reaction in which an

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Chapter 26 Solutions
General, Organic, and Biological Chemistry Seventh Edition
- 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 CH3ONA, CH3OH heat : Br:O Na → H H Br Na + H H H H H :0: .H + Undo Reset Done Q CH3 Drag To Pan +arrow_forwardWhat is the reaction mechanism for this?arrow_forward20.19 Predict the structure of the major 1,2-addition product formed by reaction of one mole of Cl₂ with 3-methylenecyclohexene. Also predict the structure of the 1,4-addition product formed under these conditions. 20.20 Which of the two molecules shown do you expect to be the major product formed by 1,2-addition of HCI to cyclopentadiene? Explain. Cyclopentadiene + HC 3-Chlorocyclopentene (racemic) or 4-Chlorocyclopentene (racemic)arrow_forward
- 20.35 Propose structural formulas for compounds A and B and specify the configuration of compound B. EtO₂C 250°C C14H2004 CO₂Et 1. Oso, then NaHSO3 2. HIO4 C14H2006 A Barrow_forward20.21 Predict the major product formed by 1,4-addition of HCI to cyclopentadiene. 20.22 Draw structural formulas for the two constitutional isomers with the molecular for- mula C₂H,Br, formed by adding one mole of Br, to cyclopentadiene.arrow_forwardAdd substituents to draw the conformer below (sighting down the indicated bond), then rotate the back carbon to provide the conformation that will be capable of an E2 elimination. R/S stereochemistry is graded. + I I H CH3 Ph Досн Br OCH 3 Drawing Q H Atoms, Bonds and Rings Charges Tap a node to see suggestions. H H H H H Undo Reset Remove Done Rotatearrow_forward
- 20.17 Predict the structure of the major product formed by 1,2-addition of HBr to 3-methylenecyclohexene. 3-Methylenecyclohexene 20.18 Predict the major product formed by 1,4-addition of HBr to 3-methylenecyclohexene.arrow_forward+ Draw a vicinal alkyl bromide that would produce the following alkene in an E2 elimination. Use a dash or wedge bond to indicate stereochemistry on asymmetric centers, where applicable. Ignore any inorganic byproducts. Br Drawing Strong Base H Q Atoms, Bonds Charges and Rings Draw or tap a new bond to see suggestions. Remove Done 語 Reset Undo + Drag To Panarrow_forwardDraw a vicinal alkyl bromide that would produce the following alkene in an E2 elimination. Use a dash or wedge bond to indicate stereochemistry on asymmetric centers, where applicable. Ignore any inorganic byproducts. + Drawing Į Strong Base H Br Q Atoms, Bonds and Rings Charges Draw or tap a new bond to see suggestions. Undo Reset 謂 Remove Done Drag To Pan +arrow_forward
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