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 51LC
Interpretation Introduction
Interpretation : The buffer system maintains the pH of a solution is to be related and effected.
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 51LC
The buffer system maintains the pH of a solution because it is made up of weak acid or weak base along with its salt.
Explanation of Solution
The equilibrium law, commonly known as Le Chatelier's principles, is used to forecast how certain changes will affect a system in
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.
The pH of the buffer is maintained at a particular value irrespective of the addition of hydrogen ions and hydroxide ions.
The buffer system is compared to Le Chatelier’s principle where the system is in equilibrium, the change occurs when the equilibrium is affected due to the surroundings.
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
- Please correct answer and don't used hand raitingarrow_forwardreciprocal lattices rotates along with the real space lattices of the crystal. true or false?arrow_forwardDeducing the reactants of a Diels-Alder reaction vn the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ? Δ O If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. • If your answer is no, check the box under the drawing area instead. Click and drag to start drawing a structure. Product can't be made in one step. Explanation Checkarrow_forward
- Predict the major products of the following organic reaction: Δ ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure. Larrow_forward> Can the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ? Δ • If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. If your answer is no, check the box under the drawing area instead. Explanation Check Click and drag to start drawing a structure. Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accesarrow_forwardPredict the major products of the following organic reaction: O O + A ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure. eserved. Terms of Use | Privacy Center >arrow_forward
- (EXM 2, PRBLM 3) Here is this problem, can you explain it to me and show how its done. Thank you I need to see the work for like prbl solving.arrow_forwardcan someone draw out the reaction mechanism for this reaction showing all bonds, intermediates and side products Comment on the general features of the 1H-NMR spectrum of isoamyl ester provided belowarrow_forwardWhat would be the best choices for the missing reagents 1 and 3 in this synthesis? 1. PPh3 3 2. n-BuLi • Draw the missing reagents in the drawing area below. You can draw them in any arrangement you like. • Do not draw the missing reagent 2. If you draw 1 correctly, we'll know what it is. • Note: if one of your reagents needs to contain a halogen, use bromine. Click and drag to start drawing a structure.arrow_forward
- Identify the missing organic reactants in the following reaction: X + Y H+ two steps 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. Click and drag to start drawing a structure. Х :arrow_forwardDraw the mechanism of friedel-crafts acylation using acetyl chloride of m-Xylenearrow_forwardI need help naming these in IUPACarrow_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 Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles 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 Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary 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