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 17, Problem 47A
(a)
Interpretation Introduction
Interpretation:
The reaction is endothermic or exothermic is to be found.
Concept Introduction:
Endothermic reactions are those reactions in which heat is absorbed. The enthalpy change for the endothermic reaction is positive.
Exothermic reactions are those reactions in which heat is released. The enthalpy change for the endothermic reaction is negative.
(a)
Expert Solution
Answer to Problem 47A
The given reaction will be exothermic.
Explanation of Solution
As it is given that when two substances in the glass beaker reacted, the beaker became too hot to touch. It means heat has been released when the two substances reacted, making the beaker absorb the released heat and thus, get hot.
(b)
Interpretation Introduction
Interpretation:
The surrounding for the given scenario is to be described.
Concept Introduction:
System is the part of the universe where observations are made and the remaining of the universe constitutes the surrounding.
(b)
Expert Solution
Answer to Problem 47A
Beaker constitutes the surrounding.
Explanation of Solution
As it is given that the two substances react, they will be under observation and will constitute the system. The beaker which is the reaction vessel will constitute the surrounding. Energy transfer takes place between the system and the surrounding.
Chapter 17 Solutions
Chemistry 2012 Student Edition (hard Cover) Grade 11
Ch. 17.1 - Prob. 1SPCh. 17.1 - Prob. 2SPCh. 17.1 - Prob. 3SPCh. 17.1 - Prob. 4SPCh. 17.1 - Prob. 5LCCh. 17.1 - Prob. 6LCCh. 17.1 - Prob. 7LCCh. 17.1 - Prob. 8LCCh. 17.1 - Prob. 9LCCh. 17.1 - Prob. 10LC
Ch. 17.1 - Prob. 11LCCh. 17.2 - Prob. 12SPCh. 17.2 - Prob. 13SPCh. 17.2 - Prob. 14SPCh. 17.2 - Prob. 15SPCh. 17.2 - Prob. 16LCCh. 17.2 - Prob. 17LCCh. 17.2 - Prob. 18LCCh. 17.2 - Prob. 19LCCh. 17.2 - Prob. 20LCCh. 17.2 - Prob. 21LCCh. 17.3 - Prob. 22SPCh. 17.3 - Prob. 23SPCh. 17.3 - Prob. 24SPCh. 17.3 - Prob. 25SPCh. 17.3 - Prob. 26SPCh. 17.3 - Prob. 27SPCh. 17.3 - Prob. 28LCCh. 17.3 - Prob. 29LCCh. 17.3 - Prob. 30LCCh. 17.3 - Prob. 31LCCh. 17.3 - Prob. 32LCCh. 17.3 - Prob. 33LCCh. 17.3 - Prob. 34LCCh. 17.4 - Prob. 35SPCh. 17.4 - Prob. 36SPCh. 17.4 - Prob. 37LCCh. 17.4 - Prob. 38LCCh. 17.4 - Prob. 39LCCh. 17.4 - Prob. 40LCCh. 17.4 - Prob. 41LCCh. 17 - Prob. 42ACh. 17 - Prob. 44ACh. 17 - Prob. 45ACh. 17 - Prob. 46ACh. 17 - Prob. 47ACh. 17 - Prob. 48ACh. 17 - Prob. 49ACh. 17 - Prob. 50ACh. 17 - Prob. 51ACh. 17 - Prob. 52ACh. 17 - Prob. 53ACh. 17 - Prob. 54ACh. 17 - Prob. 55ACh. 17 - Prob. 56ACh. 17 - Prob. 57ACh. 17 - Prob. 58ACh. 17 - Prob. 59ACh. 17 - Prob. 60ACh. 17 - Prob. 61ACh. 17 - Prob. 62ACh. 17 - Prob. 63ACh. 17 - Prob. 64ACh. 17 - Prob. 65ACh. 17 - Prob. 66ACh. 17 - Prob. 67ACh. 17 - Prob. 68ACh. 17 - Prob. 69ACh. 17 - Prob. 70ACh. 17 - Prob. 71ACh. 17 - Prob. 72ACh. 17 - Prob. 73ACh. 17 - Prob. 74ACh. 17 - Prob. 75ACh. 17 - Prob. 76ACh. 17 - Prob. 77ACh. 17 - Prob. 78ACh. 17 - Prob. 79ACh. 17 - Prob. 80ACh. 17 - Prob. 81ACh. 17 - Prob. 82ACh. 17 - Prob. 83ACh. 17 - Prob. 84ACh. 17 - Prob. 85ACh. 17 - Prob. 86ACh. 17 - Prob. 87ACh. 17 - Prob. 88ACh. 17 - Prob. 89ACh. 17 - Prob. 90ACh. 17 - Prob. 91ACh. 17 - Prob. 92ACh. 17 - Prob. 93ACh. 17 - Prob. 94ACh. 17 - Prob. 95ACh. 17 - Prob. 96ACh. 17 - Prob. 97ACh. 17 - Prob. 98ACh. 17 - Prob. 99ACh. 17 - Prob. 100ACh. 17 - Prob. 101ACh. 17 - Prob. 102ACh. 17 - Prob. 103ACh. 17 - Prob. 104ACh. 17 - Prob. 105ACh. 17 - Prob. 106ACh. 17 - Prob. 107ACh. 17 - Prob. 108ACh. 17 - Prob. 109ACh. 17 - Prob. 110ACh. 17 - Prob. 111ACh. 17 - Prob. 112ACh. 17 - Prob. 113ACh. 17 - Prob. 114ACh. 17 - Prob. 115ACh. 17 - Prob. 116ACh. 17 - Prob. 117ACh. 17 - Prob. 118ACh. 17 - Prob. 119ACh. 17 - Prob. 120ACh. 17 - Prob. 1STPCh. 17 - Prob. 2STPCh. 17 - Prob. 3STPCh. 17 - Prob. 4STPCh. 17 - Prob. 5STPCh. 17 - Prob. 6STPCh. 17 - Prob. 7STPCh. 17 - Prob. 8STPCh. 17 - Prob. 9STPCh. 17 - Prob. 10STP
Knowledge Booster
Similar questions
- Deducing 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_forwardPredict 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_forward
- Predict 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_forward
- What 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_forwardIdentify 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_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