EBK CHEMISTRY FOR ENGINEERING STUDENTS,
4th Edition
ISBN: 9781337671439
Author: Holme
Publisher: CENGAGE LEARNING - CONSIGNMENT
expand_more
expand_more
format_list_bulleted
Question
Chapter 14, Problem 14.40PAE
Interpretation Introduction
Interpretation:
To determine the mass defect in the reaction of neutron decays to a proton and an electron.
Concept introduction:
Neutron decay:
Neutrons and protons are present in the nuclei.In the neutron decay , neutron splits into an electron , proton and an antineutrino of the electron type.
The reaction of the neutron decay is as follows.
Mass defect:
The nucleus of each atom (aside from
Mass and energy are related by following equation.
E = Energy
m = mass
c =
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
1600°
1538°C
1493°C
In the diagram, the letter L indicates
that it is a liquid. Indicate its
components in the upper region
where only L is indicated.
The
iron-iron carbide phase
diagram.
Temperature (°C)
1400
8
1394°C
y+L
1200
2.14
y, Austenite
10000
912°C
800a
0.76
0.022
600
400
(Fe)
a, Ferrite
Composition (at% C)
15
1147°C
a + Fe3C
2
3
Composition (wt% C)
L
2500
4.30
2000
y + Fe3C
727°C
1500
Cementite (Fe3C)
1000
4
5
6
6.70
Temperature (°F)
None
Part II. Given below are the 'H-NMR spectrum at 300 MHz in CDC13 and mass spectrum using electron ionization
of compound Brian. The FTIR of the said compound showed a strong peak at 1710 cm").
Determine the following:
(a) molecular Formula and Degree of unsaturation of compound Brian
(b) Basing on the given H-NMR spectrum tabulate the following (i) chemical shifts
(ii) integration, ciii) multiplicity and (iv) interferences made for each signal
(c) Draw the structure of compound Brian.
)
ΕΙ
43
41
27
71
114 (M+)
Hmmm
20
30
40
50 60
70
80
90 100 110 120
1H NMR spectrum
300 MHz in CDCl3
2.0
alle
1.0
Chapter 14 Solutions
EBK CHEMISTRY FOR ENGINEERING STUDENTS,
Ch. 14 - Prob. 1COCh. 14 - Prob. 2COCh. 14 - Prob. 3COCh. 14 - Prob. 4COCh. 14 - Prob. 5COCh. 14 - Prob. 6COCh. 14 - Prob. 7COCh. 14 - Prob. 8COCh. 14 - Prob. 9COCh. 14 - Prob. 10CO
Ch. 14 - Prob. 14.1PAECh. 14 - Prob. 14.2PAECh. 14 - Prob. 14.3PAECh. 14 - Prob. 14.4PAECh. 14 - (a) How does 14C enter a living plant? (b) Write...Ch. 14 - Prob. 14.6PAECh. 14 - Prob. 14.7PAECh. 14 - Prob. 14.8PAECh. 14 - Prob. 14.9PAECh. 14 - Prob. 14.10PAECh. 14 - Prob. 14.11PAECh. 14 - Prob. 14.12PAECh. 14 - Prob. 14.13PAECh. 14 - Prob. 14.14PAECh. 14 - Prob. 14.15PAECh. 14 - Prob. 14.16PAECh. 14 - Prob. 14.17PAECh. 14 - Prob. 14.18PAECh. 14 - Prob. 14.19PAECh. 14 - Prob. 14.20PAECh. 14 - Prob. 14.21PAECh. 14 - Prob. 14.22PAECh. 14 - Prob. 14.23PAECh. 14 - Prob. 14.24PAECh. 14 - Prob. 14.25PAECh. 14 - Prob. 14.26PAECh. 14 - Prob. 14.27PAECh. 14 - Prob. 14.28PAECh. 14 - Prob. 14.29PAECh. 14 - Prob. 14.30PAECh. 14 - Prob. 14.31PAECh. 14 - Prob. 14.32PAECh. 14 - Prob. 14.33PAECh. 14 - Prob. 14.34PAECh. 14 - Prob. 14.35PAECh. 14 - Prob. 14.36PAECh. 14 - Prob. 14.37PAECh. 14 - Prob. 14.38PAECh. 14 - Prob. 14.39PAECh. 14 - Prob. 14.40PAECh. 14 - Prob. 14.41PAECh. 14 - Prob. 14.42PAECh. 14 - Prob. 14.43PAECh. 14 - Prob. 14.44PAECh. 14 - Prob. 14.45PAECh. 14 - Prob. 14.46PAECh. 14 - Prob. 14.47PAECh. 14 - Prob. 14.48PAECh. 14 - Prob. 14.49PAECh. 14 - Prob. 14.50PAECh. 14 - Prob. 14.51PAECh. 14 - Prob. 14.52PAECh. 14 - Prob. 14.53PAECh. 14 - Prob. 14.54PAECh. 14 - Prob. 14.55PAECh. 14 - Prob. 14.56PAECh. 14 - Prob. 14.57PAECh. 14 - Prob. 14.58PAECh. 14 - Prob. 14.59PAECh. 14 - Prob. 14.60PAECh. 14 - Prob. 14.61PAECh. 14 - Prob. 14.62PAECh. 14 - Prob. 14.63PAECh. 14 - Prob. 14.64PAECh. 14 - Prob. 14.65PAECh. 14 - Prob. 14.66PAECh. 14 - Prob. 14.67PAECh. 14 - Prob. 14.68PAECh. 14 - Prob. 14.69PAECh. 14 - Prob. 14.70PAECh. 14 - Prob. 14.71PAECh. 14 - Prob. 14.72PAECh. 14 - Prob. 14.73PAECh. 14 - Prob. 14.74PAECh. 14 - Prob. 14.75PAECh. 14 - Prob. 14.76PAECh. 14 - Prob. 14.77PAECh. 14 - Prob. 14.78PAECh. 14 - Prob. 14.79PAECh. 14 - Prob. 14.80PAECh. 14 - Prob. 14.81PAECh. 14 - Prob. 14.82PAECh. 14 - Prob. 14.83PAECh. 14 - Prob. 14.84PAECh. 14 - Prob. 14.85PAECh. 14 - Prob. 14.86PAECh. 14 - Prob. 14.87PAECh. 14 - Prob. 14.88PAECh. 14 - Prob. 14.89PAECh. 14 - Prob. 14.90PAECh. 14 - Prob. 14.91PAECh. 14 - Prob. 14.92PAECh. 14 - Prob. 14.93PAECh. 14 - Prob. 14.94PAECh. 14 - Prob. 14.95PAECh. 14 - Prob. 14.96PAECh. 14 - Prob. 14.97PAECh. 14 - Prob. 14.98PAECh. 14 - Prob. 14.99PAECh. 14 - Prob. 14.100PAECh. 14 - Prob. 14.101PAECh. 14 - Prob. 14.102PAECh. 14 - Prob. 14.103PAECh. 14 - Prob. 14.104PAECh. 14 - Prob. 14.105PAECh. 14 - Prob. 14.106PAECh. 14 - Prob. 14.107PAE
Knowledge Booster
Similar questions
- The iron-iron carbide phase diagram. In the diagram, the letter L indicates that it is a liquid. Indicate what its components are. Temperature (°C) 1600 10 Composition (at% C) 15 25 1538°C -1493°C 8 1400 1200 1394°C y+L L 2500 1147°C y. Austenite 2.14 4.30 2000 1000 912°C y + Fe3C 800ㅏ 0.76 0.022 600 a, Ferrite a + Fe3C 400 0 (Fe) Composition (wt% C) 727°C 1500 Cementite (Fe3C) 1000 6 6.70 Temperature (°F)arrow_forwardPart V. Choose which isomer would give the 1H-NMR spectrum below. Justify your reasoning by assigning important signals to the Corresponding protons of the correct molecule. A D on of of of H H 88 2 90 7.8 7.6 7.4 80 5 6 [ppm] 7.2 6.8 6.6 6.4 ō [ppm]arrow_forwardShow work with explanation. don't give Ai generated solutionarrow_forward
- Q7. a. Draw the line-bond structure of the major product for the following reaction, if a reaction occurs, assume monohalogenation. b. Calculate the product ratios using the following information (hint: use the number of hydrogens in each category present to calculate the ratios). Chlorination: 1° Reactivity=1 2° Reactivity=4 Heat + Cl2 3° Reactivity=5arrow_forwardPlease correct answer and don't use hand rating and don't use Ai solutionarrow_forwardQ10: Alkane halogenation a. Give the name and structures of the five isomeric hexanes. Page 4 of 5 Chem 0310 Organic Chemistry 1 Recitations b. For each isomer, give all the free radical monochlorination and monobromination products that are structurally isomeric.arrow_forward
- Q9. The insecticide DDT (in the box below) is useful in controlling mosquito populations and has low toxicity to humans, but is dangerous to birds and fish. Hoping to alleviate the dangers, little Johnny Whizbang, an aspiring chemist, proposes a new version of DDT ("Bromo-DDT") and shows his synthesis to his boss. Will Johnny Whizbang's synthesis work? Or will he be fired? Assume there is an excess of bromine and polybrominated products can be separated. Explain why. CH3 Br2, light CBR3 ok-ok Br Br Br Br CI "Bromo-DDT" CCl 3 DDT (dichlorodiphenyltrichloroethane) CIarrow_forwardDifferentiate the terms Monotectic, Eutectic, Eutectoid, Peritectic, Peritectoid.arrow_forwardQ5. Predict the organic product(s) for the following transformations. If no reaction will take place (or the reaction is not synthetically useful), write "N.R.". Determine what type of transition state is present for each reaction (think Hammond Postulate). I Br₂ CH3 F2, light CH3 Heat CH3 F₂ Heat Br2, light 12, light CH3 Cl2, lightarrow_forward
- a. For the following indicated bonds, rank them in order of decreasing AH° for homolytic cleavage. Based on your answer, which bond would be most likely to break homolytically? (a) (c) H3C CH3 .CH3 CH3 CH3 (b) Page 1 of 5 Chem 0310 Organic Chemistry 1 Recitations b. Draw all the possible radical products for 2-methylbutane, and determine which bond is most likely to be broken.arrow_forwardA 5-m³ rigid tank contains 5 kg of water at 100°C. Determine (a) the pressure, (b) the total enthalpy, and (c) the mass of each phase of water.arrow_forwardQ8. Draw the mechanism for this halogenation reaction. Show all steps including initiation, propagation, and recombination. Cl₂, hv CI Br Br2, hv, heatarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoChemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStaxChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:9781938168390
Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:OpenStax
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning