Living by Chemistry
2nd Edition
ISBN: 9781464142314
Author: Angelica M. Stacy
Publisher: W. H. Freeman
expand_more
expand_more
format_list_bulleted
Question
Chapter U5.105, Problem 1E
Interpretation Introduction
Interpretation: The change of potential energy and kinetic energy during the exothermic reaction needs to be explained.
Concept introduction: The energy in a system is a combination of potential and kinetic energy. The energy of motion is the kinetic energy and the stored energy within a physical energy is termed as potential energy.
Expert Solution & Answer
Answer to Problem 1E
In an exothermic reaction, potential energy decreases and kinetic energy increases.
Explanation of Solution
In an exothermic reaction, the potential energy of the system decreases on conversion of reactant to product because energy is conserved, that is, sum of kinetic energy and the potential energy must remain same. So, the increase of kinetic energy occurs. In exothermic reactions, the products are hotter than the reactants as they possess higher average kinetic energy.
Conclusion
In exothermic reactions, some of the potential energy converts to kinetic energy which results increase of kinetic energy.
Chapter U5 Solutions
Living by Chemistry
Ch. U5.94 - Prob. 1TAICh. U5.94 - Prob. 1ECh. U5.94 - Prob. 2ECh. U5.94 - Prob. 3ECh. U5.94 - Prob. 4ECh. U5.94 - Prob. 5ECh. U5.94 - Prob. 6ECh. U5.95 - Prob. 1TAICh. U5.95 - Prob. 1ECh. U5.95 - Prob. 2E
Ch. U5.95 - Prob. 3ECh. U5.95 - Prob. 4ECh. U5.95 - Prob. 5ECh. U5.96 - Prob. 1TAICh. U5.96 - Prob. 1ECh. U5.96 - Prob. 2ECh. U5.96 - Prob. 3ECh. U5.96 - Prob. 4ECh. U5.96 - Prob. 5ECh. U5.96 - Prob. 6ECh. U5.96 - Prob. 7ECh. U5.96 - Prob. 8ECh. U5.96 - Prob. 9ECh. U5.96 - Prob. 10ECh. U5.96 - Prob. 11ECh. U5.97 - Prob. 1TAICh. U5.97 - Prob. 1ECh. U5.97 - Prob. 2ECh. U5.97 - Prob. 3ECh. U5.97 - Prob. 4ECh. U5.97 - Prob. 5ECh. U5.97 - Prob. 6ECh. U5.97 - Prob. 7ECh. U5.98 - Prob. 1TAICh. U5.98 - Prob. 1ECh. U5.98 - Prob. 2ECh. U5.98 - Prob. 3ECh. U5.98 - Prob. 4ECh. U5.98 - Prob. 5ECh. U5.98 - Prob. 6ECh. U5.98 - Prob. 7ECh. U5.98 - Prob. 8ECh. U5.98 - Prob. 9ECh. U5.98 - Prob. 10ECh. U5.99 - Prob. 1TAICh. U5.99 - Prob. 1ECh. U5.99 - Prob. 2ECh. U5.99 - Prob. 3ECh. U5.99 - Prob. 4ECh. U5.99 - Prob. 5ECh. U5.99 - Prob. 6ECh. U5.99 - Prob. 7ECh. U5.99 - Prob. 8ECh. U5.99 - Prob. 9ECh. U5.100 - Prob. 1TAICh. U5.100 - Prob. 1ECh. U5.100 - Prob. 2ECh. U5.100 - Prob. 3ECh. U5.100 - Prob. 4ECh. U5.100 - Prob. 5ECh. U5.101 - Prob. 1TAICh. U5.101 - Prob. 1ECh. U5.101 - Prob. 2ECh. U5.101 - Prob. 3ECh. U5.101 - Prob. 4ECh. U5.101 - Prob. 6ECh. U5.102 - Prob. 1TAICh. U5.102 - Prob. 1ECh. U5.102 - Prob. 2ECh. U5.102 - Prob. 3ECh. U5.102 - Prob. 4ECh. U5.102 - Prob. 5ECh. U5.102 - Prob. 6ECh. U5.102 - Prob. 8ECh. U5.103 - Prob. 1TAICh. U5.103 - Prob. 1ECh. U5.103 - Prob. 2ECh. U5.103 - Prob. 3ECh. U5.103 - Prob. 4ECh. U5.103 - Prob. 5ECh. U5.103 - Prob. 6ECh. U5.104 - Prob. 1TAICh. U5.104 - Prob. 1ECh. U5.104 - Prob. 2ECh. U5.104 - Prob. 3ECh. U5.104 - Prob. 4ECh. U5.104 - Prob. 5ECh. U5.104 - Prob. 6ECh. U5.104 - Prob. 7ECh. U5.104 - Prob. 8ECh. U5.104 - Prob. 9ECh. U5.105 - Prob. 1TAICh. U5.105 - Prob. 1ECh. U5.105 - Prob. 2ECh. U5.105 - Prob. 3ECh. U5.105 - Prob. 4ECh. U5.105 - Prob. 5ECh. U5.106 - Prob. 1TAICh. U5.106 - Prob. 1ECh. U5.106 - Prob. 2ECh. U5.106 - Prob. 3ECh. U5.106 - Prob. 4ECh. U5.106 - Prob. 5ECh. U5.106 - Prob. 6ECh. U5.106 - Prob. 7ECh. U5.106 - Prob. 8ECh. U5.106 - Prob. 9ECh. U5.106 - Prob. 11ECh. U5.107 - Prob. 1TAICh. U5.107 - Prob. 1ECh. U5.107 - Prob. 2ECh. U5.107 - Prob. 3ECh. U5.107 - Prob. 4ECh. U5.108 - Prob. 1TAICh. U5.108 - Prob. 1ECh. U5.108 - Prob. 2ECh. U5.108 - Prob. 3ECh. U5.108 - Prob. 4ECh. U5.108 - Prob. 5ECh. U5.109 - Prob. 1TAICh. U5.109 - Prob. 1ECh. U5.109 - Prob. 2ECh. U5.109 - Prob. 3ECh. U5.109 - Prob. 4ECh. U5.109 - Prob. 5ECh. U5.109 - Prob. 6ECh. U5.109 - Prob. 7ECh. U5.109 - Prob. 8ECh. U5.110 - Prob. 1TAICh. U5.110 - Prob. 1ECh. U5.110 - Prob. 2ECh. U5.110 - Prob. 3ECh. U5.110 - Prob. 4ECh. U5.110 - Prob. 5ECh. U5.110 - Prob. 6ECh. U5.110 - Prob. 7ECh. U5.111 - Prob. 1TAICh. U5.111 - Prob. 1ECh. U5.111 - Prob. 2ECh. U5.111 - Prob. 3ECh. U5.111 - Prob. 4ECh. U5.111 - Prob. 5ECh. U5.111 - Prob. 6ECh. U5.111 - Prob. 7ECh. U5.111 - Prob. 8ECh. U5.111 - Prob. 9ECh. U5.112 - Prob. 1TAICh. U5.112 - Prob. 1ECh. U5.112 - Prob. 2ECh. U5.112 - Prob. 3ECh. U5.112 - Prob. 4ECh. U5.112 - Prob. 5ECh. U5.112 - Prob. 6ECh. U5.112 - Prob. 7ECh. U5.113 - Prob. 1TAICh. U5.113 - Prob. 1ECh. U5.113 - Prob. 2ECh. U5.113 - Prob. 3ECh. U5.113 - Prob. 4ECh. U5.113 - Prob. 5ECh. U5.113 - Prob. 6ECh. U5.113 - Prob. 7ECh. U5.113 - Prob. 8ECh. U5.114 - Prob. 1TAICh. U5.114 - Prob. 1ECh. U5.114 - Prob. 2ECh. U5.114 - Prob. 3ECh. U5.114 - Prob. 4ECh. U5.114 - Prob. 5ECh. U5.114 - Prob. 6ECh. U5.115 - Prob. 1TAICh. U5.115 - Prob. 1ECh. U5.115 - Prob. 2ECh. U5.115 - Prob. 3ECh. U5.115 - Prob. 4ECh. U5.115 - Prob. 5ECh. U5.115 - Prob. 6ECh. U5.115 - Prob. 7ECh. U5.116 - Prob. 1TAICh. U5.116 - Prob. 1ECh. U5.116 - Prob. 2ECh. U5.116 - Prob. 3ECh. U5.116 - Prob. 4ECh. U5.116 - Prob. 5ECh. U5.116 - Prob. 6ECh. U5.116 - Prob. 7ECh. U5.116 - Prob. 8ECh. U5 - Prob. C18.1RECh. U5 - Prob. C18.2RECh. U5 - Prob. C18.3RECh. U5 - Prob. C18.4RECh. U5 - Prob. C18.5RECh. U5 - Prob. C18.6RECh. U5 - Prob. C18.7RECh. U5 - Prob. C18.8RECh. U5 - Prob. C19.1RECh. U5 - Prob. C19.2RECh. U5 - Prob. C19.3RECh. U5 - Prob. C19.4RECh. U5 - Prob. C20.1RECh. U5 - Prob. C20.2RECh. U5 - Prob. C20.3RECh. U5 - Prob. C20.4RECh. U5 - Prob. C20.6RECh. U5 - Prob. C21.1RECh. U5 - Prob. C21.2RECh. U5 - Prob. C21.3RECh. U5 - Prob. C21.4RECh. U5 - Prob. C21.5RECh. U5 - Prob. 1RECh. U5 - Prob. 2RECh. U5 - Prob. 3RECh. U5 - Prob. 4RECh. U5 - Prob. 5RECh. U5 - Prob. 6RECh. U5 - Prob. 7RECh. U5 - Prob. 8RECh. U5 - Prob. 9RECh. U5 - Prob. 10RECh. U5 - Prob. 11RECh. U5 - Prob. 12RECh. U5 - Prob. 13RECh. U5 - Prob. 14RECh. U5 - Prob. 15RECh. U5 - Prob. 16RECh. U5 - Prob. 17RECh. U5 - Prob. 1STPCh. U5 - Prob. 2STPCh. U5 - Prob. 3STPCh. U5 - Prob. 4STPCh. U5 - Prob. 5STPCh. U5 - Prob. 6STPCh. U5 - Prob. 7STPCh. U5 - Prob. 8STPCh. U5 - Prob. 9STPCh. U5 - Prob. 10STPCh. U5 - Prob. 11STPCh. U5 - Prob. 12STPCh. U5 - Prob. 13STPCh. U5 - Prob. 14STPCh. U5 - Prob. 15STPCh. U5 - Prob. 16STPCh. U5 - Prob. 17STPCh. U5 - Prob. 18STPCh. U5 - Prob. 19STPCh. U5 - Prob. 20STPCh. U5 - Prob. 21STPCh. U5 - Prob. 22STP
Additional Science Textbook Solutions
Find more solutions based on key concepts
44. A student waiting at a stoplight notices that her turn signal, which has a period of 0.85 s, makes one blin...
College Physics: A Strategic Approach (3rd Edition)
Using the South Atlantic as an example, label the beginning of the normal polarity period C that began 2 millio...
Applications and Investigations in Earth Science (9th Edition)
1.1 Write a one-sentence definition for each of the following:
a. chemistry
b. chemical
Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
The genotype of F1, individuals in a tetrahybrid cross is AaBbCcDd. Assuming lndependent assortment of these fo...
Campbell Biology (11th Edition)
Modified True/False 6. __________ Halophiles inhabit extremely saline habitats, such as the Great Salt Lake.
Microbiology with Diseases by Body System (5th Edition)
All of the following terms can appropriately describe humans except: a. primary consumer b. autotroph c. hetero...
Human Biology: Concepts and Current Issues (8th Edition)
Knowledge Booster
Similar questions
- The bromination of naphthalene via electrophilic aromatic substitution. Please draw out all of the resonance structures created from addition at the C1 carbon. Please also draw out all of the resonance structures created from addition at the C2 carbon. Which carbon (C1 or C2) is more favored?arrow_forwardPredict the product or products for the following reactions. Please include both ortho and para substitutions, if it applies, and indicate the major product, if it applies.arrow_forwardChapter 1 In-Class-Problem set ☺ Study The C3-C4 carbon-carbon bond in the following molecule results from the overlap of which orbitals (in the order C3-C4)? о a) sp-sp² b) sp-sp³ c) sp²-sp² d) sp²-sp³ e) sp³-sp² 7 6 M 4 3 2arrow_forward
- Count how many pi and sigma bonds are in the following molecule, caffeine. Circle all sp3 hybridized atoms, box sp₂ hybridized atoms, and draw a triangle around all sp hybridized atoms. N N N Z - - N -arrow_forwardFill in the blanks of the following chart Characteristic Atomic Number Symbol amul Description Protons + Neutrons Use the following words to label the diagrams: Atomic Number, Valence State, Chemical Symbol, Number of Atoms, Molecule, Atomic Mass 40Ca 74W H₂O Na+¹ CI-1arrow_forwardin aqueous solution, bromine oxidises sulphur dioxide so2 to sulphate ions so42- i) deduce the oxidation state of sulphur in so2 and so4 2- ii) deduce a half equation for the reduction of bromine in an aqueous solution iii) deduce a hald equation for the oxidatio of so2 in aquoes solution forming so42- and h+ ionsarrow_forward
- Please correct answer and don't used hand raiting and don't used Ai solutionarrow_forwardDraw orbitals for a and c and identify all of the molecules/functional groups' electron geometry, molecular shape and bond angles: a. H₂O b. Ketone c. Alkyne d. Etherarrow_forwardIdentify the functional groups in the following molecule, naxalone (aka narcan): HO OH Narrow_forward
- Benzene-toluene equilibrium is often approximated as αBT = 2.34. Generate the y-x diagram for this relative volatility. Also, generate the equilibrium data using Raoult’s law, and compare your results to these. post excel spreadsheet w values used to generate both graphsarrow_forwardConvert the following structures to skeletal structures: a. CH3CH2CH2CH2COOH b. CH3CH2OCH2 Br C. CH2CHCHCHCCCHCH2arrow_forwardConvert the following structures to condensed structures: OH a. b. Cl C. Harrow_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