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.
Want to see more full solutions like this?
Chapter 26 Solutions
General, Organic, and Biological Chemistry Seventh Edition
- Please help me answer number 1. 1. If your graphs revealed a mathematical relationship between specific heat and atomic mass, write down an equation for the relationship. I also don't understand, is the equation from the line regression the one that I'm suppose use to show the relationship? If so could you work it all the way out?arrow_forwardDescribe the principle of resonance and give a set of Lewis Structures to illustrate your explanation.arrow_forwardDon't used hand raitingarrow_forward
- It is not unexpected that the methoxyl substituent on a cyclohexane ring prefers to adopt the equatorial conformation. OMe H A G₂ = +0.6 kcal/mol OMe What is unexpected is that the closely related 2-methoxytetrahydropyran prefers the axial conformation: H H OMe OMe A Gp=-0.6 kcal/mol Methoxy: CH3O group Please be specific and clearly write the reason why this is observed. This effect that provides stabilization of the axial OCH 3 group in this molecule is called the anomeric effect. [Recall in the way of example, the staggered conformer of ethane is more stable than eclipsed owing to bonding MO interacting with anti-bonding MO...]arrow_forward206 Pb 82 Express your answers as integers. Enter your answers separated by a comma. ▸ View Available Hint(s) VAΣ ΜΕ ΑΣΦ Np, N₁ = 82,126 Submit Previous Answers ? protons, neutronsarrow_forwardPlease draw the inverted chair forms of the products for the two equilibrium reactions shown below. Circle the equilibrium reaction that would have a AG = 0, i.e., the relative energy of the reactant (to the left of the equilibrium arrows) equals the relative energy of the product? [No requirement to show or do calculations.] CH3 CH3 HH CH3 1 -CH3arrow_forward
- 5. Please consider the Newman projection of tartaric acid drawn below as an eclipsed conformer (1). Please draw the most stable conformer and two intermediate energy conformers noting that staggered conformers are lower in energy than eclipsed forms even if the staggered conformers have gauche relationships between groups. [Draw the substituents H and OH on the front carbons and H, OH and CO₂H on the back carbons based on staggered forms. -CO₂H is larger than -OH.] OH COH ICOOH COOH COOH 1 2 COOH COOH 3 4 Staggered Staggered Staggered (most stable) Indicate the number of each conformer above (1, 2, 3 and 4) that corresponds to the relative energies below. Ref=0 Rotation 6. (60 points) a. Are compounds 1 and 2 below enantiomers, diastereomers or identical? OH OH HO HO LOH HO HO OH 2 OH OH b. Please complete the zig-zag conformation of the compound (3R,4S)-3,4-dichloro-2,5-dimethylhexane by writing the respective atoms in the boxes. 3.arrow_forwardThe plutonium isotope with 144 neutrons Enter the chemical symbol of the isotope.arrow_forwardThe mass ratio of sodium to fluorine in sodium fluoride is 1.21:1. A sample of sodium fluoride produced 26.1 gg of sodium upon decomposition. How much fluorine was formed?arrow_forward
- 32S 16 Enter your answers numerically separated by a comma. Np. Nn = 跖 ΟΙ ΑΣΦ Submit Request Answer ? protons, neutronsarrow_forward2. Which dimethylcyclohexane compounds shown below exhibit symmetry and therefore are not chiral and would not rotate plane polarized light. 1 CH3 CH CH3 CH3 2 3 CH3arrow_forwardDon't used hand raitingarrow_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,
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning