Essential Organic Chemistry, Global Edition
Essential Organic Chemistry, Global Edition
3rd Edition
ISBN: 9781292089034
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 2.10, Problem 33P

(a)

Interpretation Introduction

Interpretation:

The reason for pKa value of COOH group of alanine is lower than COOH group of acetic acid has to be validated.

Concept introduction:

If a base receives one proton, then the formed species is a conjugate acid whereas an acid lose one proton, then the formed species is a conjugated base.

If an acid lose one proton, then the formed species is a conjugated base. Weak base forms stronger conjugated acid.

Henderson-Hasselbalch equation explains the relationship between pH of solution and pKa of acid. For a dissociation of acid (HA) in aqueous solution,

  HA+H2OH3O++A

  pKa=pH+log[HA][A]

During a dissociation of acid in aqueous solution,

  • If pH=pKa, the concentration of compound in its acidic and basic form is equal.
  • If pH<pKa, the compound exist in its acidic form.
  • If pH>pKa, the compound exist in its basic form.

If electronegative atoms are attached to a species, it causes inductive electron withdrawal. It stabilizes its conjugate base thus increases the strength of the acid.

(b)

Interpretation Introduction

Interpretation:

Structure of alanine in solution of pH=0 has to be drawn.

Concept introduction:

If a base receives one proton, then the formed species is a conjugate acid whereas an acid lose one proton, then the formed species is a conjugated base.

If an acid lose one proton, then the formed species is a conjugated base. Weak base forms stronger conjugated acid.

Henderson-Hasselbalch equation explains the relationship between pH of solution and pKa of acid. For a dissociation of acid (HA) in aqueous solution,

  HA+H2OH3O++A

  pKa=pH+log[HA][A]

During a dissociation of acid in aqueous solution,

  • If pH=pKa, the concentration of compound in its acidic and basic form is equal.
  • If pH<pKa, the compound exist in its acidic form.
  • If pH>pKa, the compound exist in its basic form.

(c)

Interpretation Introduction

Interpretation:

Structure of alanine at pH=7.4 has to be drawn.

Concept introduction:

If a base receives one proton, then the formed species is a conjugate acid whereas an acid lose one proton, then the formed species is a conjugated base.

If an acid lose one proton, then the formed species is a conjugated base. Weak base forms stronger conjugated acid.

Henderson-Hasselbalch equation explains the relationship between pH of solution and pKa of acid. For a dissociation of acid (HA) in aqueous solution,

  HA+H2OH3O++A

  pKa=pH+log[HA][A]

During a dissociation of acid in aqueous solution,

  • If pH=pKa, the concentration of compound in its acidic and basic form is equal.
  • If pH<pKa, the compound exist in its acidic form.
  • If pH>pKa, the compound exist in its basic form.

(d)

Interpretation Introduction

Interpretation:

Structure of alanine in solution of pH=12 has to be drawn.

Concept introduction:

If a base receives one proton, then the formed species is a conjugate acid whereas an acid lose one proton, then the formed species is a conjugated base.

If an acid lose one proton, then the formed species is a conjugated base. Weak base forms stronger conjugated acid.

Henderson-Hasselbalch equation explains the relationship between pH of solution and pKa of acid.  For a dissociation of acid (HA) in aqueous solution,

  HA+H2OH3O++A

  pKa=pH+log[HA][A]

During a dissociation of acid in aqueous solution,

  • If pH=pKa, the concentration of compound in its acidic and basic form is equal.
  • If pH<pKa, the compound exist in its acidic form.
  • If pH>pKa, the compound exist in its basic form.

(e)

Interpretation Introduction

Interpretation:

The value of pH at which alanine is uncharged has to be determined.

Concept introduction:

If a base receives one proton, then the formed species is a conjugate acid whereas an acid lose one proton, then the formed species is a conjugated base.

If an acid lose one proton, then the formed species is a conjugated base. Weak base forms stronger conjugated acid.

Henderson-Hasselbalch equation explains the relationship between pH of solution and pKa of acid. For a dissociation of acid (HA) in aqueous solution,

  HA+H2OH3O++A

  pKa=pH+log[HA][A]

During a dissociation of acid in aqueous solution,

  • If pH=pKa, the concentration of compound in its acidic and basic form is equal.
  • If pH<pKa, the compound exist in its acidic form.
  • If pH>pKa, the compound exist in its basic form.

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Students have asked these similar questions
A naturally occurring amino acid such as alanine has a group that is a carboxylic acid and a group that is a protonated amine. The pKa values of the two groups are shown.(a). If the pKa value of a carboxylic acid such as acetic acid is about 5, then why is the pKa value of the carboxylic acid group of alanine so much lower? (b). Draw the structure of alanine in a solution at pH = 0. (c). Draw the structure of alanine in a solution at physiological pH (pH 7.4).(d). Draw the structure of alanine in a solution at pH = 12. (e). Is there a pH at which alanine is uncharged (that is, neither group has a charge)? (f) At what pH does alanine have no net charge (that is, the amount of negative charge is the same as the amount of positive charge)?
Some weak acids and their pKa values are given below. Which one of these acids will have the STRONGEST conjugate base? Select one: a. Phenol; pKa = 10.00 b. Methanoic acid; pKa = 3.75 c. Bromoethanoic acid; pKa = 2.9 d. Methanol; pKa = 15.54
the pKa values for phenylalanine are 1.83 (carboxyl group) and 9.13 (amino group). Use the Henderson-hasselbach equation to determine the ratio of the acidic and basic forms of each of the ionizing groups of phenylalanine at neutral pH. Based on this, draw the predominant structure of phenylalanine at neutral pH.

Chapter 2 Solutions

Essential Organic Chemistry, Global Edition

Ch. 2.3 - a. Which is a stronger base, CH3COO or HCOO? (The...Ch. 2.3 - Using the pKa values in Section 2.3, rank the...Ch. 2.4 - Prob. 13PCh. 2.5 - Prob. 14PCh. 2.5 - Ethyne has a pKa value of 25, water has a pKa...Ch. 2.5 - Which of the following bases can remove a proton...Ch. 2.6 - List the ions (CH3, NH2, HO, and F) in order from...Ch. 2.6 - List the carbanions shown in the margin in order...Ch. 2.6 - Which is a stronger acid?Ch. 2.6 - a. Draw the products of the following reactions: A...Ch. 2.6 - List the halide ions (F, Cl, Br, and I) in order...Ch. 2.6 - a. Which is more electronegative, oxygen or...Ch. 2.6 - Which is a stronger acid? a. HCl or HBr b....Ch. 2.6 - a. Which of the halide ions (F, Cl, Br, and I) is...Ch. 2.6 - Which is a stronger base? a. H2O or HO b. H2O or...Ch. 2.7 - Which is a stronger acid? a. CH3OCH2CH2OH or...Ch. 2.7 - Which is a stronger base?Ch. 2.8 - Fosamax has six acidic groups. The structure of...Ch. 2.8 - Which is a stronger acid? Why?Ch. 2.10 - For each of the following compounds (shown in...Ch. 2.10 - Prob. 33PCh. 2.11 - Write the equation that shows how a buffer made by...Ch. 2.11 - What products are formed when each of the...Ch. 2 - a. List the following alcohols in order from...Ch. 2 - Which is a stronger base? a. HS or HO b. CH3O or...Ch. 2 - Prob. 40PCh. 2 - a. List the following carboxylic acids in order...Ch. 2 - For the following compound, a. draw its conjugate...Ch. 2 - List the following compounds in order from...Ch. 2 - For each of the following compounds, draw the form...Ch. 2 - Give the products of the following acidbase...Ch. 2 - Prob. 46PCh. 2 - For each compound, indicate the atom that is most...Ch. 2 - Tenormin, a member of the group of drugs known as...Ch. 2 - From which acids can HO remove a proton in a...Ch. 2 - Prob. 50PCh. 2 - Which is a stronger acid? a. CH29CHCOOH or...Ch. 2 - Prob. 52PCh. 2 - Prob. 53PCh. 2 - How could you separate a mixture of the following...Ch. 2 - Prob. 1PCh. 2 - Prob. 2PCh. 2 - Draw the products of the following acidbase...Ch. 2 - Prob. 4PCh. 2 - Prob. 5PCh. 2 - Prob. 6PCh. 2 - Prob. 7PCh. 2 - Prob. 8PCh. 2 - Prob. 9PCh. 2 - Prob. 10PCh. 2 - Prob. 11PCh. 2 - Prob. 12PCh. 2 - Prob. 13PCh. 2 - Prob. 14P
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