Bundle: Chemistry: The Molecular Science, 5th, Loose-Leaf + OWLv2 with Quick Prep 24-Months Printed Access Card
5th Edition
ISBN: 9781305367487
Author: John W. Moore, Conrad L. Stanitski
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 14, Problem 65QRT
Interpretation Introduction
Interpretation:
The
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Please help me with # 4 and 5. Thanks in advance!
A small artisanal cheesemaker is testing the acidity of their milk
before it coagulates. During fermentation, bacteria produce lactic
acid (K₁ = 1.4 x 104), a weak acid that helps to curdle the milk and
develop flavor. The cheesemaker has measured that the developing
mixture contains lactic acid at an initial concentration of 0.025 M.
Your task is to calculate the pH of this mixture and determine whether
it meets the required acidity for proper cheese development. To
achieve the best flavor, texture and reduce/control microbial growth,
the pH range needs to be between pH 4.6 and 5.0.
Assumptions:
Lactic acid is a monoprotic acid
H
H
:0:0:
H-C-C
H
:0:
O-H
Figure 1: Lewis Structure for Lactic Acid
For simplicity, you can use the generic formula HA to represent the acid
You can assume lactic acid dissociation is in water as milk is mostly water.
Temperature is 25°C
1. Write the K, expression for the dissociation of lactic acid in the space provided. Do not forget to
include state symbols.…
Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product
structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s).
Be sure to account for all bond-breaking and bond-making steps.
:0:
:0
H.
0:0
:0:
:6:
S:
:0:
Select to Edit Arrows
::0
Select to Edit Arrows
H
:0:
H
:CI:
Rotation
Select to Edit Arrows
H.
<
:0:
:0:
:0:
S:
Chapter 14 Solutions
Bundle: Chemistry: The Molecular Science, 5th, Loose-Leaf + OWLv2 with Quick Prep 24-Months Printed Access Card
Ch. 14.1 - Identify each molecule or ion as a Brnsted-Lowry...Ch. 14.1 - Using Le Chatelier’s Principle
Use Le Chatelier’s...Ch. 14.1 - Prob. 14.3ECh. 14.1 - Complete the table.
Ch. 14.1 - Prob. 14.4ECh. 14.1 - Prob. 14.5ECh. 14.2 - Prob. 14.6CECh. 14.2 - Prob. 14.7ECh. 14.3 - Prob. 14.2PSPCh. 14.3 - Prob. 14.3PSP
Ch. 14.4 - Calculate the pH of a 0.040-M NaOH solution.
Ch. 14.4 - In a hospital laboratory the pH of a bile sample...Ch. 14.4 - Prob. 14.8CECh. 14.4 - Prob. 14.9ECh. 14.4 - Prob. 14.10ECh. 14.5 - Write the ionization equation and ionization...Ch. 14.5 - Write the ionization equation and the Kb...Ch. 14.5 - Prob. 14.11CECh. 14.5 - Prob. 14.12CECh. 14.5 - Prob. 14.13ECh. 14.6 - Prob. 14.14CECh. 14.6 - Prob. 14.15CECh. 14.6 - Prob. 14.16CECh. 14.6 - Prob. 14.17CECh. 14.6 - Prob. 14.18CECh. 14.7 - Lactic acid is a monoprotic acid that occurs...Ch. 14.7 - Prob. 14.9PSPCh. 14.7 - Prob. 14.19ECh. 14.7 - Prob. 14.10PSPCh. 14.7 - Prob. 14.20ECh. 14.8 - Prob. 14.11PSPCh. 14.8 - Prob. 14.21CECh. 14.8 - Prob. 14.12PSPCh. 14.8 - Prob. 14.22ECh. 14.8 - Prob. 14.23CECh. 14.8 - Prob. 14.24CECh. 14.9 - Predict whether each of these is a Lewis acid or a...Ch. 14.9 - Prob. 14.26ECh. 14.9 - Prob. 14.27ECh. 14.10 - Prob. 14.28ECh. 14.10 - Prob. 14.13PSPCh. 14.10 - Prob. 14.29ECh. 14.10 -
Calculate the pH of 5.2-M aqueous sodium...Ch. 14 - Lactic acid, CH3CH(OH)COOH, is a weak monoprotic...Ch. 14 - Define a Brnsted-Lowry acid and a Brnsted-Lowry...Ch. 14 - Prob. 2QRTCh. 14 - Prob. 3QRTCh. 14 - Prob. 4QRTCh. 14 - Prob. 5QRTCh. 14 - Prob. 6QRTCh. 14 - Prob. 7QRTCh. 14 - Prob. 8QRTCh. 14 - Write a chemical equation to describe the proton...Ch. 14 - Write a chemical equation to describe the proton...Ch. 14 - Prob. 11QRTCh. 14 - Prob. 12QRTCh. 14 - Prob. 13QRTCh. 14 - Prob. 14QRTCh. 14 - Prob. 15QRTCh. 14 - Prob. 16QRTCh. 14 - Prob. 17QRTCh. 14 - Prob. 18QRTCh. 14 - Prob. 19QRTCh. 14 - Prob. 20QRTCh. 14 - Prob. 21QRTCh. 14 - Prob. 22QRTCh. 14 - Prob. 23QRTCh. 14 - Formic acid, HCOOH, is found in ants. Write a...Ch. 14 - Milk of magnesia, Mg(OH)2, has a pH of 10.5....Ch. 14 - A sample of coffee has a pH of 4.3. Calculate the...Ch. 14 - Calculate the pH of a solution that is 0.025-M in...Ch. 14 - Calculate the pH of a 0.0013-M solution of HNO3....Ch. 14 - Prob. 29QRTCh. 14 - Prob. 30QRTCh. 14 - A 1000.-mL solution of hydrochloric acid has a pH...Ch. 14 - Prob. 32QRTCh. 14 - Prob. 33QRTCh. 14 - Prob. 34QRTCh. 14 - Figure 14.3 shows the pH of some common solutions....Ch. 14 - Figure 14.3 shows the pH of some common solutions....Ch. 14 - The measured pH of a sample of seawater is 8.30....Ch. 14 - Prob. 38QRTCh. 14 - Valine is an amino acid with this Lewis structure:...Ch. 14 - Leucine is an amino acid with this Lewis...Ch. 14 - Prob. 41QRTCh. 14 - Prob. 42QRTCh. 14 - Prob. 43QRTCh. 14 - Prob. 44QRTCh. 14 - Prob. 45QRTCh. 14 - Prob. 46QRTCh. 14 - Prob. 47QRTCh. 14 - Prob. 48QRTCh. 14 - Prob. 49QRTCh. 14 - Prob. 50QRTCh. 14 - Prob. 51QRTCh. 14 - Prob. 52QRTCh. 14 - Prob. 53QRTCh. 14 - Prob. 54QRTCh. 14 -
A 0.015-M solution of cyanic acid has a pH of...Ch. 14 - Prob. 56QRTCh. 14 -
The pH of a 0.10-M solution of propanoic acid,...Ch. 14 - Prob. 58QRTCh. 14 - Prob. 59QRTCh. 14 - Prob. 60QRTCh. 14 - Prob. 61QRTCh. 14 - Amantadine, C10H15NH2, is a weak base used in the...Ch. 14 - Prob. 63QRTCh. 14 -
Lactic acid, C3H6O3, occurs in sour milk as a...Ch. 14 - Prob. 65QRTCh. 14 - Complete each of these reactions by filling in the...Ch. 14 - Complete each of these reactions by filling in the...Ch. 14 - Predict which of these acid-base reactions are...Ch. 14 - Predict which of these acid-base reactions are...Ch. 14 - Prob. 70QRTCh. 14 - Prob. 71QRTCh. 14 - Prob. 72QRTCh. 14 - Prob. 73QRTCh. 14 - Prob. 74QRTCh. 14 - Prob. 75QRTCh. 14 - Prob. 76QRTCh. 14 - Prob. 77QRTCh. 14 - Prob. 78QRTCh. 14 - Prob. 79QRTCh. 14 - Prob. 80QRTCh. 14 - Prob. 81QRTCh. 14 - Trimethylamine, (CH3)3N, reacts readily with...Ch. 14 - Prob. 83QRTCh. 14 - Prob. 84QRTCh. 14 - Prob. 85QRTCh. 14 - Prob. 86QRTCh. 14 - Common soap is made by reacting sodium carbonate...Ch. 14 - Prob. 88QRTCh. 14 - Prob. 89QRTCh. 14 - Prob. 90QRTCh. 14 - Prob. 91QRTCh. 14 - Prob. 92QRTCh. 14 - Prob. 93QRTCh. 14 -
Several acids and their respective equilibrium...Ch. 14 - Prob. 95QRTCh. 14 - Prob. 96QRTCh. 14 - Does the pH of the solution increase, decrease, or...Ch. 14 - Does the pH of the solution increase, decrease, or...Ch. 14 - Prob. 99QRTCh. 14 - Prob. 100QRTCh. 14 - Prob. 101QRTCh. 14 - Prob. 102QRTCh. 14 - Prob. 103QRTCh. 14 - Prob. 104QRTCh. 14 - Prob. 105QRTCh. 14 - Prob. 106QRTCh. 14 - When all the water is evaporated from a sodium...Ch. 14 - Prob. 108QRTCh. 14 - Prob. 109QRTCh. 14 - Prob. 110QRTCh. 14 - Prob. 111QRTCh. 14 - Prob. 112QRTCh. 14 - Prob. 113QRTCh. 14 - Prob. 114QRTCh. 14 - Prob. 115QRTCh. 14 - Prob. 116QRTCh. 14 - Home gardeners spread aluminum sulfate powder...Ch. 14 - Prob. 118QRTCh. 14 - Prob. 119QRTCh. 14 - Prob. 120QRTCh. 14 - Prob. 121QRTCh. 14 - Prob. 122QRTCh. 14 - Prob. 123QRTCh. 14 - Prob. 124QRTCh. 14 - Prob. 125QRTCh. 14 - A chilled carbonated beverage is opened and warmed...Ch. 14 - Prob. 127QRTCh. 14 -
Explain why BrNH2 is a weaker base than ammonia,...Ch. 14 - Prob. 129QRTCh. 14 - Prob. 130QRTCh. 14 - At 25 C, a 0.10% aqueous solution of adipic acid,...Ch. 14 - Prob. 132QRTCh. 14 - Prob. 133QRTCh. 14 - Prob. 134QRTCh. 14 - Prob. 135QRTCh. 14 - Prob. 14.ACPCh. 14 - Develop a set of rules by which you could predict...
Knowledge Booster
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
- 3:48 PM Fri Apr 4 K Problem 4 of 10 Submit Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Mg. :0: Select to Add Arrows :0: :Br: Mg :0: :0: Select to Add Arrows Mg. Br: :0: 0:0- Br -190 H 0:0 Select to Add Arrows Select to Add Arrows neutralizing workup H CH3arrow_forwardIarrow_forwardDraw the Markovnikov product of the hydrobromination of this alkene. Note for advanced students: draw only one product, and don't worry about showing any stereochemistry. Drawing dash and wedge bonds has been disabled for this problem. + Explanation Check 1 X E 4 1 1 1 1 1 HBr Click and drag to start drawing a structure. 80 LE #3 @ 2 $4 0 I அ2 % 85 F * K M ? BH 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center & 6 27 FG F10 8 9 R T Y U D F G H P J K L Z X C V B N M Q W A S H option command H command optiarrow_forward
- Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products. Predict the major products of the following reaction. Explanation Q F1 A Check F2 @ 2 # 3 + X 80 F3 W E S D $ 4 I O H. H₂ 2 R Pt % 05 LL ee F6 F5 T <6 G Click and drag to start drawing a structure. 27 & A 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center Acce Y U H DII 8 9 F10 4 J K L Z X C V B N M T H option command F11 P H commandarrow_forwardCurved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the intermediate and product in this reaction or mechanistic step(s). Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore inorganic byproducts. H :0: CH3 O: OH Q CH3OH2+ Draw Intermediate protonation CH3OH CH3OH nucleophilic addition H Draw Intermediate deprotonation :0: H3C CH3OH2* protonation H 0: H CH3 H.arrow_forwardPredicting the reactants or products of hemiacetal and acetal formation uentify the missing organic reactants in the following reaction: H+ X+Y OH H+ за Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H2O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Explanation Check Click and drag to start drawing a structure. ? olo 18 Ar © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forward
- can someone please answer thisarrow_forwardPlease, please help me figure out the the moles, molarity and Ksp column. Step by step details because I've came up with about three different number and have no idea what I'm doing wrong.arrow_forwardwhat reagents are used to get this product from this reactant? Br OCH3arrow_forward
- can someone answer this pleasearrow_forwardcan someone do the reaction mechanism for this reaction and draw the molecules for Q2 and q3arrow_forwardIn this question, the product of the aldol condensation is shown. What would be the reactants for this product? Please provide a detailed explanation, as well as a drawing showing how the reactants will react to produce the product.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
Principles of Modern ChemistryChemistryISBN:9781305079113Author:David W. Oxtoby, H. Pat Gillis, Laurie J. ButlerPublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Principles of Modern Chemistry
Chemistry
ISBN:9781305079113
Author:David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
General Chemistry | Acids & Bases; Author: Ninja Nerd;https://www.youtube.com/watch?v=AOr_5tbgfQ0;License: Standard YouTube License, CC-BY