Organic Chemistry, Books A La Carte Edition (7th Edition)
Organic Chemistry, Books A La Carte Edition (7th Edition)
7th Edition
ISBN: 9780321819031
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 2, Problem 55P

(a)

Interpretation Introduction

Interpretation:

The product for the given acid-base reaction has to written and whether the reaction is product favored or reactant favored at equilibrium has to be indicated.

Concept introduction:

According to the explanations by Bronsted-Lowry, if a species loses a proton then it is an acid whereas if a species receives one proton, then it is base.

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.

Mixture of acid and base undergoes equilibrium reaction and it’s pKa-values determine their direction of reaction.

Weak acids are more stable and less reactive, so equilibrium follows the direction of formation weak acids in a reaction.

Lesser the pKa- value of compound will be more acidic. So the equilibrium follows the direction of compounds having low pKa-value to the products of high pKa value

(b)

Interpretation Introduction

Interpretation:

The product for the given acid-base reaction has to written and whether the reaction is product favored or reactant favored at equilibrium has to be indicated.

Concept introduction:

According to the explanations by Bronsted-Lowry, if a species loses a proton then it is an acid whereas if a species receives one proton, then it is base.

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.

Mixture of acid and base undergoes equilibrium reaction and it’s pKa-values determine their direction of reaction.

Weak acids are more stable and less reactive, so equilibrium follows the direction of formation weak acids in a reaction.

Lesser the pKa- value of compound will be more acidic. So the equilibrium follows the direction of compounds having low pKa-value to the products of high pKa value

(c)

Interpretation Introduction

Interpretation:

The product for the given acid-base reaction has to written and whether the reaction is product favored or reactant favored at equilibrium has to be indicated.

Concept introduction:

According to the explanations by Bronsted-Lowry, if a species loses a proton then it is an acid whereas if a species receives one proton, then it is base.

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.

Mixture of acid and base undergoes equilibrium reaction and it’s pKa-values determine their direction of reaction.

Weak acids are more stable and less reactive, so equilibrium follows the direction of formation weak acids in a reaction.

Lesser the pKa- value of compound will be more acidic. So the equilibrium follows the direction of compounds having low pKa-value to the products of high pKa value

(d)

Interpretation Introduction

Interpretation:

The product for the given acid-base reaction has to written and whether the reaction is product favored or reactant favored at equilibrium has to be indicated.

Concept introduction:

According to the explanations by Bronsted-Lowry, if a species loses a proton then it is an acid whereas if a species receives one proton, then it is base.

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.

Mixture of acid and base undergoes equilibrium reaction and it’s pKa-values determine their direction of reaction.

Weak acids are more stable and less reactive, so equilibrium follows the direction of formation weak acids in a reaction.

Lesser the pKa- value of compound will be more acidic. So the equilibrium follows the direction of compounds having low pKa-value to the products of high pKa value

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Chapter 2 Solutions

Organic Chemistry, Books A La Carte Edition (7th Edition)

Ch. 2.3 - Estimate the pKa values of the following...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. 14PCh. 2.5 - a. For each of the acid-base reactions in Section...Ch. 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. 2.5 - Calculate the equilibrium constant for the...Ch. 2.6 - Rank the ions (CH3, NH2, HO, and F) from most...Ch. 2.6 - Rank the carbanions shown in the margin from most...Ch. 2.6 - Which is the stronger acid?Ch. 2.6 - Prob. 22PCh. 2.6 - Rank the halide ions (F, Cl, Br, and l) from...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 l) is...Ch. 2.6 - Prob. 27PCh. 2.7 - What is a stronger acid? a. CH3OCH2CH2OH or...Ch. 2.7 - Prob. 29PCh. 2.7 - What is a stronger base?Ch. 2.8 - Fosamax (shown on the previous page) has six...Ch. 2.8 - Which is a stronger acid? Why?Ch. 2.8 - Prob. 34PCh. 2.9 - Using the table of pKa values given in Appendix I,...Ch. 2.10 - Prob. 36PCh. 2.10 - As long as the pH is not less than _______, at...Ch. 2.10 - A naturally occurring amino acid such as alanine...Ch. 2.10 - For each of the following compounds, indicate the...Ch. 2.11 - Write the equation that shows how a buffer made by...Ch. 2.12 - Draw the products of the following react ions. Use...Ch. 2.12 - What product are formed when each of the following...Ch. 2 - a. Rank the following alcohols from strongest to...Ch. 2 - Which is a stronger base? a. HS or HO b. CH3O or...Ch. 2 - According to the explanations by Lewis, if a...Ch. 2 - a. Rank the following carboxylic acids from...Ch. 2 - Prob. 51PCh. 2 - For the following compound. a. draw its conjugate...Ch. 2 - Rank the following compounds from strongest to...Ch. 2 - Prob. 54PCh. 2 - Prob. 55PCh. 2 - a. Rank the following alcohols from strongest to...Ch. 2 - For each compound, indicate the atom that is most...Ch. 2 - a. Given the Ka values, estimate the pKa value of...Ch. 2 - A single bond between two carbons with different...Ch. 2 - Tenormin, a member of the group of drugs known as...Ch. 2 - From which of the following compounds can HO...Ch. 2 - a. For each of the following pairs of reactions,...Ch. 2 - Prob. 63PCh. 2 - Which is a stronger acid? a. b. c. d.Ch. 2 - Prob. 65PCh. 2 - Given that pH+ pOH = 14 and that the concentration...Ch. 2 - How could you separate a mixture of the following...Ch. 2 - Prob. 68PCh. 2 - a. If an add with a pKa of 5.3 is in an aqueous...Ch. 2 - Calculate the pH values of the following...Ch. 2 - Prob. 1PCh. 2 - Prob. 2PCh. 2 - Prob. 3PCh. 2 - Which of the reactions in Problem 3 favor...Ch. 2 - Prob. 5PCh. 2 - Prob. 6PCh. 2 - Prob. 7PCh. 2 - Which is the stronger acid? a. ClCH2CH2OH or...Ch. 2 - Prob. 9PCh. 2 - Prob. 10PCh. 2 - Which is a more stable base? Remembering that the...Ch. 2 - Which is the Stronger acid?Ch. 2 - Prob. 13PCh. 2 - a. Draw the structure of (CH3COOH (pKa = 4.7) at...
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