
Chemistry 2012 Student Edition (hard Cover) Grade 11
12th Edition
ISBN: 9780132525763
Author: Prentice Hall
Publisher: Prentice Hall
expand_more
expand_more
format_list_bulleted
Question
Chapter 19.5, Problem 47LC
Interpretation Introduction
Interpretation : The type of substance combined to make a buffer solution is to be described.
Concept Introduction : A buffer is a solution that retains the pH of a solution irrespective of the addition of small amounts of acids or bases.
Expert Solution & Answer

Answer to Problem 47LC
Either weak acid or base along with its respective salts constitutes a buffer solution.
Explanation of Solution
A weak acid and one of its salts or a weak base and one of its salts are solutions that are used as buffers.
Buffers are formed by the combination of weak acids or bases with their respective salts.
For example, ethanoic acid-ethanoate ion buffer, and ammonium ion-ammonia buffer.
Chapter 19 Solutions
Chemistry 2012 Student Edition (hard Cover) Grade 11
Ch. 19.1 - Prob. 1SPCh. 19.1 - Prob. 2SPCh. 19.1 - Prob. 3LCCh. 19.1 - Prob. 4LCCh. 19.1 - Prob. 5LCCh. 19.1 - Prob. 6LCCh. 19.1 - Prob. 7LCCh. 19.1 - Prob. 8LCCh. 19.1 - Prob. 9LCCh. 19.2 - Prob. 10SP
Ch. 19.2 - Prob. 11SPCh. 19.2 - Prob. 12SPCh. 19.2 - Prob. 13SPCh. 19.2 - Prob. 14SPCh. 19.2 - Prob. 15SPCh. 19.2 - Prob. 16SPCh. 19.2 - Prob. 17SPCh. 19.2 - Prob. 18LCCh. 19.2 - Prob. 19LCCh. 19.2 - Prob. 20LCCh. 19.2 - Prob. 21LCCh. 19.2 - Prob. 22LCCh. 19.2 - Prob. 23LCCh. 19.2 - Prob. 24LCCh. 19.3 - Prob. 25SPCh. 19.3 - Prob. 26SPCh. 19.3 - Prob. 27LCCh. 19.3 - Prob. 28LCCh. 19.3 - Prob. 29LCCh. 19.3 - Prob. 30LCCh. 19.3 - Prob. 31LCCh. 19.3 - Prob. 32LCCh. 19.3 - Prob. 33LCCh. 19.3 - Prob. 34LCCh. 19.4 - Prob. 35SPCh. 19.4 - Prob. 36SPCh. 19.4 - Prob. 37SPCh. 19.4 - Prob. 38SPCh. 19.4 - Prob. 39LCCh. 19.4 - Prob. 40LCCh. 19.4 - Prob. 41LCCh. 19.4 - Prob. 42LCCh. 19.4 - Prob. 43LCCh. 19.5 - Prob. 44SPCh. 19.5 - Prob. 45SPCh. 19.5 - Prob. 46LCCh. 19.5 - Prob. 47LCCh. 19.5 - Prob. 48LCCh. 19.5 - Prob. 49LCCh. 19.5 - Prob. 50LCCh. 19.5 - Prob. 51LCCh. 19 - Prob. 52ACh. 19 - Prob. 53ACh. 19 - Prob. 54ACh. 19 - Prob. 55ACh. 19 - Prob. 56ACh. 19 - Prob. 57ACh. 19 - Prob. 58ACh. 19 - Prob. 59ACh. 19 - Prob. 60ACh. 19 - Prob. 61ACh. 19 - Prob. 62ACh. 19 - Prob. 63ACh. 19 - Prob. 64ACh. 19 - Prob. 65ACh. 19 - Prob. 66ACh. 19 - Prob. 67ACh. 19 - Prob. 68ACh. 19 - Prob. 69ACh. 19 - Prob. 70ACh. 19 - Prob. 71ACh. 19 - Prob. 72ACh. 19 - Prob. 73ACh. 19 - Prob. 74ACh. 19 - Prob. 75ACh. 19 - Prob. 76ACh. 19 - Prob. 77ACh. 19 - Prob. 78ACh. 19 - Prob. 79ACh. 19 - Prob. 80ACh. 19 - Prob. 81ACh. 19 - Prob. 82ACh. 19 - Prob. 83ACh. 19 - Prob. 84ACh. 19 - Prob. 85ACh. 19 - Prob. 86ACh. 19 - Prob. 87ACh. 19 - Prob. 88ACh. 19 - Prob. 89ACh. 19 - Prob. 90ACh. 19 - Prob. 91ACh. 19 - Prob. 92ACh. 19 - Prob. 93ACh. 19 - Prob. 94ACh. 19 - Prob. 95ACh. 19 - Prob. 96ACh. 19 - Prob. 97ACh. 19 - Prob. 98ACh. 19 - Prob. 99ACh. 19 - Prob. 100ACh. 19 - Prob. 101ACh. 19 - Prob. 102ACh. 19 - Prob. 103ACh. 19 - Prob. 104ACh. 19 - Prob. 105ACh. 19 - Prob. 106ACh. 19 - Prob. 107ACh. 19 - Prob. 108ACh. 19 - Prob. 109ACh. 19 - Prob. 110ACh. 19 - Prob. 111ACh. 19 - Prob. 112ACh. 19 - Prob. 113ACh. 19 - Prob. 114ACh. 19 - Prob. 117ACh. 19 - Prob. 118ACh. 19 - Prob. 119ACh. 19 - Prob. 120ACh. 19 - Prob. 121ACh. 19 - Prob. 122ACh. 19 - Prob. 123ACh. 19 - Prob. 124ACh. 19 - Prob. 125ACh. 19 - Prob. 126ACh. 19 - Prob. 127ACh. 19 - Prob. 128ACh. 19 - Prob. 129ACh. 19 - Prob. 130ACh. 19 - Prob. 131ACh. 19 - Prob. 132ACh. 19 - Prob. 133ACh. 19 - Prob. 134ACh. 19 - Prob. 135ACh. 19 - Prob. 136ACh. 19 - Prob. 137ACh. 19 - Prob. 138ACh. 19 - Prob. 139ACh. 19 - Prob. 1STPCh. 19 - Prob. 2STPCh. 19 - Prob. 3STPCh. 19 - Prob. 4STPCh. 19 - Prob. 5STPCh. 19 - Prob. 6STPCh. 19 - Prob. 7STPCh. 19 - Prob. 8STPCh. 19 - Prob. 9STPCh. 19 - Prob. 10STPCh. 19 - Prob. 11STPCh. 19 - Prob. 12STPCh. 19 - Prob. 13STP
Knowledge Booster
Similar questions
- Can I please get the blank spaces answered/answers?arrow_forward1. Identify the following alkenes as E or Z NH₂ Br 2. Draw the structures based on the IUPAC names (3R,4R)-3-bromo-4-fluoro- 1-hexene (Z)-4-bromo-2-iodo-3-ethyl- 3-heptene تر 3. For the following, predict all possible elimination product(s) and circle the major product. HO H₂SO4 Heat 80 F4 OH H2SO4 Heat 어요 F5 F6 1 A DII 4 F7 F8 F9 % & 5 6 7 * ∞ 8 BAB 3 E R T Y U 9 F D G H J K O A F11 F10arrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts. ○ O 1. H₂O, pyridine 2. neutralizing work-up a N W X 人 Parrow_forward
- ✓ Check the box under each molecule that has a total of five ẞ hydrogens. If none of the molecules fit this description, check the box underneath the table. tab OH CI 0 Br xx Br None of these molecules have a total of five ẞ hydrogens. esc Explanation Check caps lock shift 1 fn control 02 F2 W Q A N #3 S 80 F3 E $ t 01 205 % 5 F5 & 7 © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility FT * 8 R T Y U כ F6 9 FIG F11 F D G H J K L C X V B < N M H option command P H + F12 commandarrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts and the carboxylic acid side product. O 1. CHзMgBr (excess) 2. H₂O ✓ W X 人arrow_forwardIf cyclopentyl acetaldehyde reacts with NaOH, state the product (formula).arrow_forward
- Draw the major product of this reaction. Ignore inorganic byproducts. N S S HgCl2, H2SO4 く 8 W X Parrow_forwardtab esc く Drawing the After running various experiments, you determine that the mechanism for the following reaction occurs in a step-wise fashion. Br + OH + Using this information, draw the correct mechanism in the space below. 1 Explanation Check F2 F1 @2 Q W A os lock control option T S # 3 80 F3 Br $ 4 0105 % OH2 + Br Add/Remove step X C F5 F6 6 R E T Y 29 & 7 F D G H Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Ce A F7 DII F8 C Ո 8 * 9 4 F10 F C J K L C V Z X B N M H command P ge Coarrow_forwardIndicate compound A that must react with ethylbenzene to obtain 4-ethylbenzene-1-sulfonic acid. 3-bromo-4-ethylbenzene-1-sulfonic acid.arrow_forward
- Part 1 of 2 Draw the structure of A, the minor E1 product of the reaction. esc I Skip Part Check H₂O, D 2 A + Click and drag to start drawing a structure. -0- F1 F2 1 2 # 3 Q A 80 F3 W E S D F4 $ 4 % 5 F5 ㅇ F6 R T Y F G X 5 & 7 + Save 2025 McGraw Hill LLC. All Rights Reserved. DII F7 F8 H * C 80 J Z X C V B N 4 F9 6arrow_forwardFile Preview The following is a total synthesis of the pheromone of the western pine beetle. Such syntheses are interesting both because of the organic chemistry, and because of the possibility of using species specific insecticides, rather than broad band insecticides. Provide the reagents for each step. There is some chemistry from our most recent chapter in this synthesis, but other steps are review from earlier chapters. (8 points) COOEt COOEt A C COOEt COOEt COOH B OH OTS CN D E See the last homework set F for assistance on this one. H+, H₂O G OH OH The last step is just nucleophilic addition reactions, taking the ketone to an acetal, intramolecularly. But it is hard to visualize the three dimensional shape as it occurs. Frontalin, pheromone of the western pine beetlearrow_forwardFor the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. C Major Product: Check + ◎ + X ง © Cl I F2 80 F3 I σ F4 I F5 NaOH Click and drawing F6 A 2025 McGraw Hill LLC. All Rights E F7 F8 $ # % & 2 3 4 5 6 7 8 Q W E R T Y U A S D F G H Jarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY

Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education

Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning

Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education

Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning

Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY