Introduction to General, Organic and Biochemistry
Introduction to General, Organic and Biochemistry
11th Edition
ISBN: 9781285869759
Author: Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher: Cengage Learning
bartleby

Concept explainers

Question
Book Icon
Chapter 18, Problem 18.36P
Interpretation Introduction

Interpretation:

The form of ascorbic acid and ascorbate anion in blood plasma should be determined.

Concept Introduction:

For an acid HA; the acid dissociation reaction can be written as.

HA+H2OA+H3O+

The acid dissociation constant (Ka) is the ratio of product and reactant for the acid dissociation reaction. Hence it can be written as;.

Ka=[A][H3O+][HA]

Henderson-Hasselbalch equation purposed the relation between pH and pKa for weak acids:

pH=pKa+log[A][HA].

Blurred answer
Students have asked these similar questions
The Ka1 of ascorbic acid is 7.94 x 10-5. Would you expect ascorbic acid dissolved in blood plasma (pH 7.35–7.45) to exist primarily as ascorbic acid or as ascorbate anion? Explain.
The Ka1 of ascorbic acid is 7.94 x 10°. Would you expect ascorbic acid dissolved in blood plasma (pH 7.35-7.45) to exist primarily as ascorbic acid or as ascorbate anion? From the choices provided below, indicate whether the carboxylic acid will exist primarily in its protonated form as a Free Acid or in its deprotonated form as a Carboxylate Anion by clicking on the corresponding button. At equilibrium in this pH, the concentration of the preferred form of the acid is approximately times higher than the concentration of its conjugate form. Round to the nearest order of magnitude.
The Brønsted-Lowry definition of acids and bases is: Acids are proton donors, bases are proton acceptors Acids are nucleophiles and bases are electrophiles Acids are proton acceptors, bases are proton donors Carboxy groups are acids and amine groups are bases Carboxy groups are electrophiles and amine groups are nucelophiles

Chapter 18 Solutions

Introduction to General, Organic and Biochemistry

Ch. 18 - Prob. 18.11PCh. 18 - Prob. 18.12PCh. 18 - Prob. 18.13PCh. 18 - 18-14 Answer true or false. (a) Carboxylic acids...Ch. 18 - 18-15 Draw a structural formula for the dimer...Ch. 18 - 18-16 Propanedioic (malonic) acid forms an...Ch. 18 - 18-17 Hexanoic (caproic) acid has a solubility in...Ch. 18 - 18-18 Propanoic acid and methyl acetate are...Ch. 18 - 18-19 The following compounds have approximately...Ch. 18 - Prob. 18.20PCh. 18 - Prob. 18.21PCh. 18 - Prob. 18.22PCh. 18 - 18-23 Characterize the structural features...Ch. 18 - Prob. 18.24PCh. 18 - Prob. 18.25PCh. 18 - 18-26 Answer true or false. (a) Carboxylic acids...Ch. 18 - Prob. 18.27PCh. 18 - 18-28 Arrange these compounds in order of...Ch. 18 - 18-29 Complete the equations for these acid—base...Ch. 18 - 18-30 Complete the equations for these acid-base...Ch. 18 - 18-31 Formic acid is one of the components...Ch. 18 - Prob. 18.32PCh. 18 - Prob. 18.33PCh. 18 - Prob. 18.34PCh. 18 - Prob. 18.35PCh. 18 - Prob. 18.36PCh. 18 - Prob. 18.37PCh. 18 - 18-38 Which is the stronger base: CH3CH2NH2 or...Ch. 18 - Prob. 18.39PCh. 18 - Prob. 18.40PCh. 18 - 18-41 Complete these examples of Fischer...Ch. 18 - Prob. 18.42PCh. 18 - Prob. 18.43PCh. 18 - Prob. 18.44PCh. 18 - Prob. 18.45PCh. 18 - 18-46 Procaine (its hydrochloride salt is marketed...Ch. 18 - 18-47 Methylparaben and propylparaben are used as...Ch. 18 - 18-48 4-Aminobenzoic acid is prepared from benzoic...Ch. 18 - Prob. 18.49PCh. 18 - Prob. 18.50PCh. 18 - Prob. 18.51PCh. 18 - Prob. 18.52PCh. 18 - Prob. 18.53PCh. 18 - Prob. 18.54PCh. 18 - Prob. 18.55P
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
Recommended textbooks for you
Text book image
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Text book image
Macroscale and Microscale Organic Experiments
Chemistry
ISBN:9781305577190
Author:Kenneth L. Williamson, Katherine M. Masters
Publisher:Brooks Cole