
World of Chemistry, 3rd edition
3rd Edition
ISBN: 9781133109655
Author: Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher: Brooks / Cole / Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 19, Problem 39A
Interpretation Introduction
Interpretation: The functions of various parts of nuclear reactor are to be described.
Concept introduction: Because of the emission of large energy nuclear fission has been developed as an energy source to produce electricity in reactors where controlled fission can occur. The resulting energy is used to heat water to produce steam that runs turbine which in turn runs the electric generator.
Expert Solution & Answer

Answer to Problem 39A
The major components of the nuclear reactor are moderator, reactor coolant, control rods, and containment shell.
Explanation of Solution
- Neutrons produced by nuclear reactions move too fast to cause fission. A moderator slows down the neutrons so that the uranium fuel can capture them more efficiently.
- Coolant is used to carry the heat produced by the fission reaction to an external boiler and turbine, where it is converted into electricity. Many nuclear power plants uses light water as a coolant.
- Control rods, made up of substances such as cadmium, boron and hafnium that absorb neutrons and are used to regulate the rate of the chain reaction.
- A nuclear reactor produces neutrons and other decay products that remains radioactive and emits radiation. Apart from that, a nuclear reactor is thermally very hot and high pressures result from the circulation of water or another coolant through it. Thus, a reactor must tolerate such high temperatures and pressures and must protect operating personnel from the radiation. Reactors are equipped with a containment shield to do this job.
Conclusion
The major components of the nuclear reactor are moderator, reactor coolant, control rods, and containment shell.
Chapter 19 Solutions
World of Chemistry, 3rd edition
Ch. 19.1 - Prob. 1RQCh. 19.1 - Prob. 2RQCh. 19.1 - Prob. 3RQCh. 19.1 - Prob. 4RQCh. 19.1 - Prob. 5RQCh. 19.1 - Prob. 6RQCh. 19.1 - Prob. 7RQCh. 19.2 - Prob. 1RQCh. 19.2 - Prob. 2RQCh. 19.2 - Prob. 3RQ
Ch. 19.2 - Prob. 4RQCh. 19.3 - Prob. 1RQCh. 19.3 - Prob. 2RQCh. 19.3 - Prob. 3RQCh. 19.3 - Prob. 4RQCh. 19.3 - Prob. 5RQCh. 19.3 - Prob. 6RQCh. 19 - Prob. 1ACh. 19 - Prob. 2ACh. 19 - Prob. 3ACh. 19 - Prob. 4ACh. 19 - Prob. 5ACh. 19 - Prob. 6ACh. 19 - Prob. 7ACh. 19 - Prob. 8ACh. 19 - Prob. 9ACh. 19 - Prob. 10ACh. 19 - Prob. 11ACh. 19 - Prob. 12ACh. 19 - Prob. 13ACh. 19 - Prob. 14ACh. 19 - Prob. 15ACh. 19 - Prob. 16ACh. 19 - Prob. 17ACh. 19 - Prob. 18ACh. 19 - Prob. 19ACh. 19 - Prob. 20ACh. 19 - Prob. 21ACh. 19 - Prob. 22ACh. 19 - Prob. 23ACh. 19 - Prob. 24ACh. 19 - Prob. 25ACh. 19 - Prob. 26ACh. 19 - Prob. 27ACh. 19 - Prob. 28ACh. 19 - Prob. 29ACh. 19 - Prob. 30ACh. 19 - Prob. 31ACh. 19 - Prob. 32ACh. 19 - Prob. 33ACh. 19 - Prob. 34ACh. 19 - Prob. 35ACh. 19 - Prob. 36ACh. 19 - Prob. 37ACh. 19 - Prob. 38ACh. 19 - Prob. 39ACh. 19 - Prob. 40ACh. 19 - Prob. 41ACh. 19 - Prob. 42ACh. 19 - Prob. 43ACh. 19 - Prob. 44ACh. 19 - Prob. 45ACh. 19 - Prob. 46ACh. 19 - Prob. 47ACh. 19 - Prob. 48ACh. 19 - Prob. 49ACh. 19 - Prob. 50ACh. 19 - Prob. 51ACh. 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. 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. 12STP
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
- Predict the major organic product(s) of the following reactions. Indicate which of the following mechanisms is in operation: SN1, SN2, E1, or E2.arrow_forward(c) (4pts) Mechanism: heat (E1) CH3OH + 1.5pts each _E1 _ (1pt) Br CH3OH (d) (4pts) Mechanism: SN1 (1pt) (e) (3pts) 1111 I H 10 Ill!! H LDA THF (solvent) Mechanism: E2 (1pt) NC (f) Bri!!!!! CH3 NaCN (3pts) acetone Mechanism: SN2 (1pt) (SN1) -OCH3 OCH3 1.5pts each 2pts for either product 1pt if incorrect stereochemistry H Br (g) “,、 (3pts) H CH3OH +21 Mechanism: SN2 (1pt) H CH3 2pts 1pt if incorrect stereochemistry H 2pts 1pt if incorrect stereochemistryarrow_forwardA mixture of butyl acrylate and 4'-chloropropiophenone has been taken for proton NMR analysis. Based on this proton NMR, determine the relative percentage of each compound in the mixturearrow_forward
- Q5: Label each chiral carbon in the following molecules as R or S. Make sure the stereocenter to which each of your R/S assignments belong is perfectly clear to the grader. (8pts) R OCH 3 CI H S 2pts for each R/S HO R H !!! I OH CI HN CI R Harrow_forwardCalculate the proton and carbon chemical shifts for this structurearrow_forwardA. B. b. Now consider the two bicyclic molecules A. and B. Note that A. is a dianion and B. is a neutral molecule. One of these molecules is a highly reactive compound first characterized in frozen noble gas matrices, that self-reacts rapidly at temperatures above liquid nitrogen temperature. The other compound was isolated at room temperature in the early 1960s, and is a stable ligand used in organometallic chemistry. Which molecule is the more stable molecule, and why?arrow_forward
- A mixture of C7H12O2, C9H9OCl, biphenyl and acetone was put together in a gas chromatography tube. Please decide from the GC resutls which correspond to the peak for C7,C9 and biphenyl and explain the reasoning based on GC results. Eliminate unnecessary peaks from Gas Chromatography results.arrow_forwardIs the molecule chiral, meso, or achiral? CI .CH3 H₂C CIarrow_forwardPLEASE HELP ! URGENT!arrow_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