Textbook Question
For the bases shown, draw the conjugate acid and identify a pKa value from Table 4.5 that would help you accurately estimate its stability.
(d)
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Ch. 4 - Acids and Bases: Electron Flow
Mullins1st EditionOrganic Chemistry: A Learner Centered ApproachISBN: 9780137566471
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Table of contents
- Ch. 2 - General Chemistry Translated: Finding the Electrons114
- Ch. 3 - Alkanes and Cycloalkanes: Properties and Conformational Analysis109
- Ch. 4 - Acids and Bases: Electron Flow144
- Ch. 5 - Chemical Reaction Analysis: Thermodynamics and Kinetics118
- Ch. 6 - Stereoisomerism: Arrangement of Atoms in Space112
- Ch. 7 - Principles of Green (Organic) Chemistry3
- Ch. 8 - Alkenes I: Properties and Electrophilic Additions158
- Ch. 9 - Alkenes II: Oxidation and Reduction150
- Ch. 10 - Alkynes: Electrophilic Addition and Redox Reactions101
- Ch. 11 - Properties and Synthesis of Alkyl Halides: Radical Reactions108
- Ch. 12 - Substitution and Elimination: Reactions of Haloalkanes172
- Ch. 13 - Alcohols, Ethers and Related Compounds: Substitution and Elimination239
- Ch. 14 - Structural Identification I: Infrared Spectroscopy and Mass Spectrometry54
- Ch. 15 - Structural Identification II: Nuclear Magnetic Resonance Spectroscopy93
- Ch. 16 - Metals in Organic Chemistry48
- Ch. 17 - Carbonyl Addition Reactions: Aldehydes and Ketones45
- Ch. 18 - Nucleophilic Acyl Substitution I: Carboxylic Acids18
- Ch. 19 - Nucleophilic Acyl Substitution II: Carboxylic Acid Derivatives39
- Ch. 20 - Enolates: Carbonyl Addition and Substitution13
- Ch. 21 - Conjugated Systems I: Stability and Addition Reactions56
- Ch. 22 - Conjugated Systems II: Pericyclic Reactions54
- Ch. 23 - Benzene I: Aromatic Stability and Substitution Reactions64
- Ch. 24 - Benzene II: Reactions Influenced by the Aromatic Ring62
- Ch. 25 - Amines: Structure, Reactions, and Synthesis27
- Ch. 26 - Amino Acids, Proteins, and Peptide Synthesis9
- Ch. 27 - Carbohydrates, Nucleic Acids, and Lipids54
Mullins1st EditionOrganic Chemistry: A Learner Centered ApproachISBN: 9780137566471Not the one you use?Change textbook
Chapter 3, Problem 40b
For the bases shown, draw the conjugate acid and identify a pKa value from Table 4.5 that would help you accurately estimate its stability.
(b) 
Verified step by step guidance1
Identify the base in the problem. A base is a species that can accept a proton (H⁺). Look for lone pairs of electrons or negative charges that can act as proton acceptors.
Draw the conjugate acid of the base by adding a proton (H⁺) to the base. This involves attaching the proton to the atom with the lone pair or negative charge. Ensure the formal charges are updated correctly after the addition of the proton.
Refer to Table 4.5 (or the relevant pKₐ table) to find the pKₐ value of the conjugate acid. The pKₐ value provides information about the strength of the conjugate acid and indirectly about the stability of the base.
Use the pKₐ value to estimate the stability of the base. A higher pKₐ value for the conjugate acid indicates a weaker acid, which corresponds to a more stable base. Conversely, a lower pKₐ value indicates a stronger acid and a less stable base.
Compare the stability of the base with other bases if needed, using the pKₐ values of their conjugate acids. This comparison can help you rank the bases in terms of their relative stability.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Conjugate Acids and Bases
In acid-base chemistry, a conjugate acid is formed when a base accepts a proton (H⁺). Understanding this concept is crucial for predicting the behavior of substances in reactions. For example, when ammonia (NH₃) acts as a base, it can accept a proton to form ammonium (NH₄⁺), its conjugate acid.
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Equilibrium constant and conjugates.
pKₐ and Acid Strength
The pKₐ value is a quantitative measure of the strength of an acid in solution; it indicates the tendency of an acid to donate a proton. A lower pKₐ value corresponds to a stronger acid, which is more likely to lose a proton. This concept is essential for comparing the stability of conjugate acids formed from different bases.
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Stability of Conjugate Acids
The stability of a conjugate acid is influenced by factors such as electronegativity, resonance, and inductive effects. A more stable conjugate acid will have a lower pKₐ, indicating that it is less likely to donate a proton. Analyzing these factors helps in estimating the relative strengths of acids and bases in chemical reactions.
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Related Practice
Textbook Question
For each indicated proton, suggest an approximate pKa value from Table 4.5. Rationalize your choice.
(b)
1
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Textbook Question
For each indicated proton, suggest an approximate pKa value from Table 4.5. Rationalize your choice.
(d)
2
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Textbook Question
Calculate Keq for these acid–base reactions.
(d)
1
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Textbook Question
For the bases shown, draw the conjugate acid and identify a pKa value from Table 4.5 that would help you accurately estimate its stability.
(c)
1
views
Textbook Question
For the bases shown, draw the conjugate acid and identify a pKa value from Table 4.5 that would help you accurately estimate its stability.
(e)
2
views