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pH, pKa and Acid/Base Strength

Related Topics

Organic Chemistry 1 Textbook > Acid/Base Chemistry & Intro to Organic Reactions

Factors Influencing Acid/Base Strength

5 Activities

Organic Chemistry 1 Textbook > Acid/Base Chemistry & Intro to Organic Reactions

Relationship Between pH and pKa

7 Activities

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What are the predominant structures in solution of L-glutamic acid (shown below) at pH = 2, 7, and 12. The relevant pKas are: carboxylic acid (4) and protonated amine (10).


More Factors Influencing Acid/Base Strength Questions:
Acids and Bases: Equilibria
Practice: Acid/Base Equilibrium
Which way does the equilibrium lie in the following reactions?
Practice: Acid/Base Equilibria,
Which way does the equilibrium lie in the following reactions?
Acids and Bases: Equilibrium
Which way does the equilibrium lie in the following reactions (right/left)?
Practice: Rank the following compounds from least acidic to most acidic: phenol, ethanol, and 4-nitrophenol. Justify your ranking using ARIO principles.
Practice: Ranking Acid Strength
For each set of molecules below, rank them in order of increasing acidity (from 1 = least acidic to 4 = most acidic). Provide a brief justification for your ranking, referencing the key ARIO principles (Atom, Resonance, Induction, Orbital).
Problem Set 1:
Practice: Which of the following is the strongest acid?
Practice: Ranking Acid Strength
Which of the following is the strongest acid?
A) H₂O (pKa ≈ 15.7)





Stability of Conjugate Base
Compare the acidity of the following molecules:
Indicate (Left/Right) the species with the more acidic proton in each pair, rationalize your choice.
Species 1:
Species 2:
Indicate which direction the equilibrium lies in the following examples (Left/Right)
Example 1:
Example 2:








Acids and Bases: Equilibria
Practice: Acid/Base Equilibrium
Which way does the equilibrium lie in the following reactions?
Acids and Bases: Equilibrium
Practice: Acid/Base Equilibrium
Which way does the equilibrium lie in the following reactions (right/left)?
Acidity & Resonance
1. Compare the acidity of the highlighted H atoms:
2. Explain why the highlighted H shown in 1 is more acidic than the one shown in 2:
Base Strength
1. Compare the basicity of the following molecules:
2.
Stability of Conjugate Base
Compare the acidity of the following molecules:
Acids and Bases
Which of the following molecules is the strongest Lewis Base?
CH4, BF3, NH3, NaOH
Acids and Bases
Which one is the strongest acid and why? Explain using resonance:
Base Strength & Resonance
Choose the more basic compound in each pair:
1.
2.
Acids and Bases: Acidity
Which of the following compounds has the most acidic hydrogen?
Acids and bases equilibrium
Select the answer which correctly shows the proton movement and has the correct side indicated as being favored.
Rank (numerical order 1,2,3,4,5,....) the following nitrogen anions in terms of basicity. 1 is the most basic.
A)
B)
Acids and Bases: Factors affecting strength
Rank (numerical order 1,2,3,4,5,....) the following in terms of increasing acidity. 1 is the most acidic Rationalize your ranking below.
A)
B)
Acid/Base Equilibria
Which way does the equilibrium lie in the following reactions?
Acid/Base Equilibria
Which way does the equilibrium lie in the following reactions?
Acids/Bases Stength vs. pH and pKa
The pKa of a phenol functionality (Ph-OH) is approximately 10. Draw the predominant structures of L-Tyrosine (shown below) at pH = 2, 7 and 12. Additional relevant pKas are: carboxylic acid (4) and protonated amine (10).
Which of the following is the strongest Lewis Base?
Acids and Bases: Strength

Acids and Bases: Strength

Equilibrium: Acids and Bases/Stability



Equilibrium: Acids and Bases

Chemical reactions: Acids and Bases

Acids and Bases: Strength
Indicate (Left/Right) the species with the more acidic proton in each pair, rationalize your choice.
Species 1:
Species 2:
Equilibrium: Acids and Bases

Equilibrium: Acids and Bases

Equilibrium: Acids and Bases

Chemical reactions: Acids and Bases

Equilibrium: Acids and Bases

Acids and Bases: Strength
Indicate which direction the equilibrium lies in the following examples (Left/Right)
Example 1:
Example 2:
More Relationship Between pH and pKa Questions:
Practice: Amino Acids in Solution
Practice: Amino acids pKa
The pKa of a phenol functionality (Ph-OH) is approximately 10. Draw the predominant structures of L-Tyrosine (shown below) at pH = 2, 7 and 12.
Amino acids pKa
Practice: Amino Acids pKa
What are the predominant structures in solution of L-glutamic acid (shown below) at pH = 2, 7, and 12?
Amino acids pKa
Practice: Amino Acids pKa
The pKa of a phenol functionality (Ph-OH) is approximately 10. Draw the predominant structures of L-Tyrosine (shown below) at pH = 2, 7 and 12.
Amino acids pKa
Practice: Amino Acids in Solution
What are the predominant structures in solution of L-glutamic acid (shown below) at pH = 2, 7, and 12?
pH, pKa and amino acids
What are the predominant structures in solution of L-glutamic acid (shown below) at pH = 2, 7, and 12
pH, pKa and amino acids
The pKa of a phenol functionality (Ph-OH) is approximately 10. Draw the predominant structures of L-Tyrosine (shown below) at pH = 2, 7 and 12
Acids/Bases Stength vs. pH and pKa
The pKa of a phenol functionality (Ph-OH) is approximately 10. Draw the predominant structures of L-Tyrosine (shown below) at pH = 2, 7 and 12. Additional relevant pKas are: carboxylic acid (4) and protonated amine (10).