
Concept explainers
(a)
Interpretation: To determine whether oxaloacetate and
Concept introduction: Transamination reaction is a biochemical reaction that involves the transfer of an amino group. In transamination reaction exchange of an amino group from an
The general structure of an amino acid is:
Here,
An acid containing both carbonyl and carboxyl
(a)

Answer to Problem 26.33EP
No, oxaloacetate and
Explanation of Solution
Oxaloacetate is a keto acid and its structure is:
The two reactants in transamination reaction are a keto acid and an amino acid. Both oxaloacetate and
(b)
Interpretation: To determine whether glutamate and oxaloacetate could function as the two reactants in a transamination reaction or not.
Concept introduction: Transamination reaction is a biochemical reaction that involves the transfer of an amino group. In transamination reaction exchange of an amino group from an
The general structure of an amino acid is:
Here,
An acid containing both carbonyl and carboxyl functional group is known as a keto acid. A general representation of a keto acid is:
(b)

Answer to Problem 26.33EP
Yes, glutamate and oxaloacetate can function as the reactants in a transamination reaction.
Explanation of Solution
Glutamate is an amino acid and its structure is:
Oxaloacetate is a keto acid and its structure is:
Transamination reaction involves the exchange of an amino group from an
(c)
Interpretation: To determine whether glutarate and glutamate could function as the two reactants in a transamination reaction or not.
Concept introduction: Transamination reaction is a biochemical reaction that involves the transfer of an amino group. In transamination reaction exchange of an amino group from an
The general structure of an amino acid is:
Here,
An acid containing both carbonyl and carboxyl functional group is known as a keto acid. A general representation of a keto acid is:
(c)

Answer to Problem 26.33EP
No, glutarate and glutamate cannot function as the reactants in a transamination reaction.
Explanation of Solution
Glutarate is a diacid and its structure is:
Glutamate is an amino acid and its structure is:
The two reactants in transamination reaction are a keto acid and an amino acid. Glutamate is an amino acid but glutarate is not a keto acid. For a transamination reaction to take place there must be one keto acid present along with an amino acid. Thus, glutarate and glutamate cannot function as the reactants in a transamination reaction.
(d)
Interpretation: To determine whether oxaloacetate and succinate could function as the two reactants in a transamination reaction or not.
Concept introduction: Transamination reaction is a biochemical reaction that involves the transfer of an amino group. In transamination reaction exchange of an amino group from an
The general reaction to illustrate transamination is as follows:
The general structure of an amino acid is:
Here,
An acid containing both carbonyl and carboxyl functional group is known as a keto acid. A general representation of a keto acid is:
(d)

Answer to Problem 26.33EP
No, oxaloacetate and succinate cannot function as the reactants in a transamination reaction.
Explanation of Solution
Oxaloacetate is a keto acid and its structure is:
Succinate is a diacid acid and its structure is:
The two reactants in transamination reaction are a keto acid and an amino acid. Oxaloacetate is keto acid but succinate is not an amino acid. For a transamination reaction to take place there must be one amino acid present along with a keto acid. Thus, oxaloacetate and succinate cannot function as the reactants in a transamination reaction.
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Chapter 26 Solutions
General, Organic, and Biological Chemistry Seventh Edition
- What is the reaction mechanism for this?arrow_forwardPredict the major products of both organic reactions. Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products. esc esc Explanation Check 2 : + + X H₁₂O + Х ง WW E R Y qab Ccaps lock shift $ P X Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility Bil T FR F18 9 G t K L Z X V B N M control opption command command T C darrow_forwardDraw the Markovnikov product of the hydrohalogenation of this alkene. this problem. Note for advanced students: draw only one product, and don't worry about showing any stereochemistry. Drawing dash and wedge bonds has been disabled for caps lock Explanation Check 2 W E R + X 5 HCI Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility Bil Y F G H K L ZZ X C V B N M control opption command F10 F10 command 4 BA Ar Carrow_forward
- I don't understand why the amide on the top left, with the R attached to one side, doesn't get substituted with OH to form a carboxylic acid. And if only one can be substituted, why did it choose the amide it chose rather than the other amide?arrow_forwardesc Draw the Markovnikov product of the hydration of this alkene. Note for advanced students: draw only one product, and don't worry about showing any stereochemistry. Drawing dash and wedge bonds has been disabled for this problem. Explanation Check BBB + X 0 1. Hg (OAc)2, H₂O 2. Na BH 5 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility Bl P 豆 28 2 28 N 9 W E R T Y A S aps lock G H K L Z X C V B N M T central H command #e commandarrow_forwardC A student proposes the transformation below in one step of an organic synthesis. There may be one or more products missing from the right-hand side, but there are no reagents missing from the left-hand side. There may also be catalysts, small inorganic reagents, and other important reaction conditions missing from the arrow. • Is the student's transformation possible? If not, check the box under the drawing area. . If the student's transformation is possible, then complete the reaction by adding any missing products to the right-hand side, and adding required catalysts, inorganic reagents, or other important reaction conditions above and below the arrow. • You do not need to balance the reaction, but be sure every important organic reactant or product is shown. (X) This transformation can't be done in one step. + Tarrow_forward
- く Predict the major products of this organic reaction. If there aren't any products, because nothing will happen, check the box under the drawing area instead. No reaction. Explanation Check OH + + ✓ 2 H₂SO 4 O xs H₂O 2 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forwardDraw the skeletal ("line") structure of 1,3-dihydroxy-2-pentanone. Click and drag to start drawing a structure. X Parrow_forwardPredicting edict the major products of this organic reaction. If there aren't any products, because nothing will happen, check the box under the drawing area instead. + No reaction. Explanation Check HO Na O H xs H₂O 2 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Iarrow_forward
- Choosing reagents and conditions for acetal formation or hydrolysis 0/5 A student proposes the transformation below in one step of an organic synthesis. There may be one or more products missing from the right-hand side, but there are no reagents missing from the left-hand side. There may also be catalysts, small inorganic reagents, and other important reaction conditions missing from the arrow. • Is the student's transformation possible? If not, check the box under the drawing area. If the student's transformation is possible, then complete the reaction by adding any missing products to the right-hand side, and adding required catalysts, inorganic reagents, or other important reaction conditions above and below the arrow. • You do not need to balance the reaction, but be sure every important organic reactant or product is shown. + This transformation can't be done in one step. 5 I H Autumn alo 值 Ar Barrow_forwardA block of copper of mass 2.00kg(cp = 0.3851 .K) and g temperature 0°C is introduced into an insulated container in which there is 1.00molH, O(g) at 100°C and 1.00 2 atm. Note that C P = 4.184. K for liquid water, and g that A H = 2260 for water. vap g Assuming all the steam is condensed to water, and that the pressure remains constant: (a) What will be the final temperature of the system? (b) What is the heat transferred from the water to the copper? (c) What is the entropy change of the water, the copper, and the total system?arrow_forwardIdentify the missing organic reactants in the following reaction: H+ X + Y OH H+ O O Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H₂O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Explanation Check Click and drag to start drawing a structure. X G 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Cente ? Earrow_forward
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