Chemistry
4th Edition
ISBN: 9780078021527
Author: Julia Burdge
Publisher: McGraw-Hill Education
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 8, Problem 29QP
Interpretation Introduction
Interpretation:
The single, double, and triple bonds in a molecule and theirrespective bond lengthsare to be compared.
Concept introduction:
A single bond forms between two atoms when two atoms share a single electron between them.
A double bond forms between two atoms when two atoms share two electrons between them.
A triple bond forms between two atoms when two atoms share three electrons between them.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Hi!!
Please provide a solution that is handwritten. Ensure all figures, reaction mechanisms (with arrows and lone pairs please!!), and structures are clearly drawn to illustrate the synthesis of the product as per the standards of a third year organic chemistry course. ****the solution must include all steps, mechanisms, and intermediate structures as required.
Please hand-draw the mechanisms and structures to support your explanation. Don’t give me AI-generated diagrams or text-based explanations, no wordy explanations on how to draw the structures I need help with the exact mechanism hand drawn by you!!! I am reposting this—ensure all parts of the question are straightforward and clear or please let another expert handle it thanks!!
Hi!!
Please provide a solution that is handwritten. Ensure all figures, reaction mechanisms (with arrows and lone pairs please!!), and structures are clearly drawn to illustrate the synthesis of the product as per the standards of a third year organic chemistry course. ****the solution must include all steps, mechanisms, and intermediate structures as required.
Please hand-draw the mechanisms and structures to support your explanation. Don’t give me AI-generated diagrams or text-based explanations, no wordy explanations on how to draw the structures I need help with the exact mechanism hand drawn by you!!! I am reposting this—ensure all parts of the question are straightforward and clear or please let another expert handle it thanks!!
. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the
molecule depicted below.
Bond B
2°C. +2°C. < cleavage
Bond A
• CH3 + 26. t cleavage
2°C• +3°C•
Bond C
Cleavage
CH3 ZC
'2°C. 26.
E
Strongest
3°C. 2C.
Gund
Largest
BDE
weakest bond
In that molecule
a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in
appropriate boxes.
Weakest
C bond
Produces
A
Weakest
Bond
Most
Strongest
Bond
Stable radical
Strongest Gund
produces least stable
radicals
b. (4pts) Consider the relative stability of all cleavage products that form when bonds A,
B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B,
and C are all carbon radicals.
i. Which ONE cleavage product is the most stable? A condensed or bond line
representation is fine.
人
8°C. formed in
bound C
cleavage
ii. Which ONE cleavage product is the least stable? A condensed or bond line
representation is fine.
methyl radical
•CH3
formed in
bund A Cleavage
Chapter 8 Solutions
Chemistry
Ch. 8.1 - Practice ProblemATTEMPT Write Lewis dot symbols...Ch. 8.1 - Practice Problem BUILD
Indicate the charge on...Ch. 8.1 - Practice ProblemCONCEPTUALIZE For each of the...Ch. 8.1 - 8.1.1 Using only a periodic table, determine the...Ch. 8.1 - 8.1.2 Using only a periodic table, determine the...Ch. 8.1 - To which group does element X belong if its Lewis...Ch. 8.1 - Prob. 4CPCh. 8.2 - Prob. 1PPACh. 8.2 - Practice ProblemBUILD Arrange the compounds NaF,...Ch. 8.2 - Practice ProblemCONCEPTUALIZE Common ions of four...
Ch. 8.2 - 8.2.1 Will the lattice energy of KF be larger or...Ch. 8.2 - 8.2.2 Using the following data, calculate the...Ch. 8.2 - 8.2.3 Lattice energies are graphed for three...Ch. 8.3 - Practice ProblemATTEMPT Using data from Figures...Ch. 8.3 - Prob. 1PPBCh. 8.3 - Prob. 1PPCCh. 8.4 - Practice Problem ATTEMPT Classify the following...Ch. 8.4 - Prob. 1PPBCh. 8.4 - Prob. 1PPCCh. 8.4 - In which of the following molecules are the bonds...Ch. 8.4 - Using data from Table 8.5, calculate the magnitude...Ch. 8.4 - Prob. 3CPCh. 8.4 - Prob. 4CPCh. 8.5 - Prob. 1PPACh. 8.5 - Prob. 1PPBCh. 8.5 - Prob. 1PPCCh. 8.5 - Identify the correct Lewis structure for formic...Ch. 8.5 - Identity the correct Lewis structure for hydrogen...Ch. 8.6 - Prob. 1PPACh. 8.6 - Prob. 1PPBCh. 8.6 - Prob. 1PPCCh. 8.6 - Determine the formal charges on H, C, and N,...Ch. 8.6 - 8.6.2 Which of the Lewis structures shown is most...Ch. 8.7 - Prob. 1PPACh. 8.7 - Practice ProblemBUILD Draw the Lewis structure for...Ch. 8.7 - Practice Problem CONCEPTUALIZE
Of the three Lewis...Ch. 8.7 - Indicate which of the following are resonance...Ch. 8.7 - 8.7.2 How many resonance structures can be drawn...Ch. 8.8 - Prob. 1PPACh. 8.8 - Prob. 1PPBCh. 8.8 - Practice Problem CONCEPTUALIZE
The hypothetical...Ch. 8.8 - In which of the following species does the central...Ch. 8.8 - Prob. 2CPCh. 8.8 - In which species does the central atom obey the...Ch. 8.8 - 8.8.4 How many lone pairs are there on the central...Ch. 8.9 - Prob. 1PPACh. 8.9 - Practice ProblemBUILD Use Lewis structures and...Ch. 8.9 - Prob. 1PPCCh. 8.9 - 8.9.1 Use data from Table 8.6 to estimate for the...Ch. 8.9 - Use data from Table 8.6 to estimate Δ H rxn for...Ch. 8.9 - Use bond enthalpies to determine Δ H rxn for the...Ch. 8.9 - Prob. 4CPCh. 8.10 - Practice ProblemATTEMPT Draw all possible...Ch. 8.10 - Prob. 1PPBCh. 8.10 - Practice ProblemCONCEPTUALIZE The Lewis structure...Ch. 8.11 - Prob. 1PPACh. 8.11 - Prob. 1PPBCh. 8.11 - Prob. 1PPCCh. 8.12 - Prob. 1PPACh. 8.12 - Prob. 1PPBCh. 8.12 - Prob. 1PPCCh. 8.13 - Prob. 1PPACh. 8.13 - Practice Problem BUILD
Using the following...Ch. 8.13 - Prob. 1PPCCh. 8 - 8.1
Which of the following atoms must always obey...Ch. 8 - Prob. 2KSPCh. 8 - Prob. 3KSPCh. 8 - Prob. 4KSPCh. 8 - What is a Lewis dot symbol? What elements do we...Ch. 8 - Use the second member of each group from Group 1A...Ch. 8 - Prob. 3QPCh. 8 - 8.4 Write Lewis dot symbols for the following...Ch. 8 - Write Lewis dot symbols for the following atoms...Ch. 8 - Prob. 6QPCh. 8 - Prob. 7QPCh. 8 - Name five metals and five nonmetals that are very...Ch. 8 - Prob. 9QPCh. 8 - Prob. 10QPCh. 8 - Prob. 11QPCh. 8 - The term molar mass was introduced in Chapter 3....Ch. 8 - Prob. 13QPCh. 8 - Prob. 14QPCh. 8 - Prob. 15QPCh. 8 - Explain how the lattice energy of an ionic...Ch. 8 - Prob. 17QPCh. 8 - Prob. 18QPCh. 8 - 8.19 Use the Born-Haber cycle outlined in Section...Ch. 8 - Calculate the lattice energy of CaCl 2 . Use data...Ch. 8 - An ionic bond is formed between a cation A + and...Ch. 8 - Prob. 22QPCh. 8 - Use Lewis dot symbols to show the transfer of...Ch. 8 - Write the Lewis dot symbols of the reactants and...Ch. 8 - 8.25 Describe Lewis’s contribution to our...Ch. 8 - Prob. 26QPCh. 8 - Prob. 27QPCh. 8 - Prob. 28QPCh. 8 - Prob. 29QPCh. 8 - Prob. 30QPCh. 8 - Prob. 31QPCh. 8 - Prob. 32QPCh. 8 - Prob. 33QPCh. 8 - Define electronegativity, and explain the...Ch. 8 - Prob. 35QPCh. 8 - Prob. 36QPCh. 8 - Prob. 37QPCh. 8 - Using information in Table 8.5. calculate the...Ch. 8 - List the following bonds in order of increasing...Ch. 8 - Classify the following bonds as covalent, polar...Ch. 8 - 8.41 Classify the following bonds as covalent,...Ch. 8 - 8.42 List the following bonds in order of...Ch. 8 - Prob. 43QPCh. 8 - Prob. 44QPCh. 8 - Prob. 45QPCh. 8 - Prob. 46QPCh. 8 - Draw Lewis structures for the following molecules...Ch. 8 - Draw Lewis structures for the following molecules:...Ch. 8 - Prob. 49QPCh. 8 - Prob. 50QPCh. 8 - 8.51 Draw Lewis structures for the following ions:...Ch. 8 - Draw Lewis structures for the following ions: (a)...Ch. 8 - Prob. 53QPCh. 8 - Prob. 54QPCh. 8 - Prob. 55QPCh. 8 - Prob. 56QPCh. 8 - Prob. 57QPCh. 8 - 8.58 Draw three resonance structures for the...Ch. 8 - Prob. 59QPCh. 8 - Prob. 60QPCh. 8 - Draw three reasonable resonance structures for the...Ch. 8 - Draw three resonance structures for the molecule N...Ch. 8 - Prob. 63QPCh. 8 - Prob. 64QPCh. 8 - Prob. 65QPCh. 8 - Prob. 66QPCh. 8 - Prob. 67QPCh. 8 - Prob. 68QPCh. 8 - Prob. 69QPCh. 8 - The AlI 3 molecule has an incomplete octet around...Ch. 8 - Prob. 71QPCh. 8 - Prob. 72QPCh. 8 - 8.73 Write a Lewis structure for Does this...Ch. 8 - Prob. 74QPCh. 8 - Prob. 75QPCh. 8 - 8.76 Draw two resonance structures for the bromate...Ch. 8 - Prob. 77QPCh. 8 - What is bond enthalpy? Bond enthalpies of...Ch. 8 - Prob. 79QPCh. 8 - Prob. 80QPCh. 8 - Prob. 81QPCh. 8 - Prob. 82QPCh. 8 - For the reaction 2 C 2 H 6 ( g ) + 7 O 2 ( g ) → 4...Ch. 8 - Prob. 84QPCh. 8 - 8.85. Use average bond enthalpies from Table 8.6...Ch. 8 - Prob. 86APCh. 8 - Prob. 87APCh. 8 - Prob. 88APCh. 8 - Prob. 89APCh. 8 - Prob. 90APCh. 8 - 8.91 Describe some characteristics of an ionic...Ch. 8 - Prob. 92APCh. 8 - Prob. 93APCh. 8 - Prob. 94APCh. 8 - Prob. 95APCh. 8 - Prob. 96APCh. 8 - Prob. 97APCh. 8 - Prob. 98APCh. 8 - Prob. 99APCh. 8 - Prob. 100APCh. 8 - Prob. 101APCh. 8 - Prob. 102APCh. 8 - Prob. 103APCh. 8 - Prob. 104APCh. 8 - Which of the following species are isoelectronic:...Ch. 8 - Prob. 106APCh. 8 - 8.107 Draw two resonance structures for each...Ch. 8 - The following species have been detected in...Ch. 8 - The amide ion ( NH 2 − ) is a Brø�nsted base. Use...Ch. 8 - Prob. 110QPCh. 8 - The triiodide ion ( I 3 − ) in which the I atoms...Ch. 8 - Prob. 112APCh. 8 - In 1999, an unusual cation containing only...Ch. 8 - Prob. 114APCh. 8 - Prob. 115APCh. 8 - Prob. 116APCh. 8 - In the gas phase, aluminum chloride exists as a...Ch. 8 - Prob. 118APCh. 8 - Calculate Δ H º for the reaction H 2 ( g ) + I 2 (...Ch. 8 - Draw Lewis structures for the following organic...Ch. 8 - Prob. 121APCh. 8 - Prob. 122APCh. 8 - Prob. 123APCh. 8 - Write three resonance structures for (a) the...Ch. 8 - Prob. 125APCh. 8 - Prob. 126APCh. 8 - Prob. 127APCh. 8 - Prob. 128APCh. 8 - Prob. 129APCh. 8 - Prob. 130APCh. 8 - Prob. 131APCh. 8 - Among the common inhaled anesthetics are:...Ch. 8 - Prob. 133QPCh. 8 - Prob. 134QPCh. 8 - Prob. 135QPCh. 8 - 8.136 Using this and data from Appendix 2,...Ch. 8 - Prob. 137QPCh. 8 - Prob. 138APCh. 8 - Prob. 139APCh. 8 - Prob. 140APCh. 8 - Prob. 141APCh. 8 - Prob. 142APCh. 8 - Prob. 143APCh. 8 - Although nitrogen dioxide ( NO 2 ) is a stable...Ch. 8 - 8.145 The chlorine nitrate molecule is believed...Ch. 8 - The hydroxyl radical ( OH ) plays an important...Ch. 8 - Prob. 147APCh. 8 - Prob. 148APCh. 8 - Prob. 1SEPPCh. 8 - 2. Use formal charges to choose the best of the...Ch. 8 - Prob. 3SEPPCh. 8 - Prob. 4SEPP
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
- Which carbocation is more stable?arrow_forwardAre the products of the given reaction correct? Why or why not?arrow_forwardThe question below asks why the products shown are NOT the correct products. I asked this already, and the person explained why those are the correct products, as opposed to what we would think should be the correct products. That's the opposite of what the question was asking. Why are they not the correct products? A reaction mechanism for how we arrive at the correct products is requested ("using key intermediates"). In other words, why is HCl added to the terminal alkene rather than the internal alkene?arrow_forward
- My question is whether HI adds to both double bonds, and if it doesn't, why not?arrow_forwardStrain Energy for Alkanes Interaction / Compound kJ/mol kcal/mol H: H eclipsing 4.0 1.0 H: CH3 eclipsing 5.8 1.4 CH3 CH3 eclipsing 11.0 2.6 gauche butane 3.8 0.9 cyclopropane 115 27.5 cyclobutane 110 26.3 cyclopentane 26.0 6.2 cycloheptane 26.2 6.3 cyclooctane 40.5 9.7 (Calculate your answer to the nearest 0.1 energy unit, and be sure to specify units, kJ/mol or kcal/mol. The answer is case sensitive.) H. H Previous Nextarrow_forwardA certain half-reaction has a standard reduction potential Ered +1.26 V. An engineer proposes using this half-reaction at the anode of a galvanic cell that must provide at least 1.10 V of electrical power. The cell will operate under standard conditions. Note for advanced students: assume the engineer requires this half-reaction to happen at the anode of the cell. Is there a minimum standard reduction potential that the half-reaction used at the cathode of this cell can have? If so, check the "yes" box and calculate the minimum. Round your answer to 2 decimal places. If there is no lower limit, check the "no" box.. Is there a maximum standard reduction potential that the half-reaction used at the cathode of this cell can have? If so, check the "yes" box and calculate the maximum. Round your answer to 2 decimal places. If there is no upper limit, check the "no" box. yes, there is a minimum. 1 red Πν no minimum Oyes, there is a maximum. 0 E red Dv By using the information in the ALEKS…arrow_forward
- (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B Bond A Bond C a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. Weakest Bond Strongest Bond b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. c. (5pts) Use principles discussed in lecture, supported by relevant structures, to succinctly explain the why your part b (i) radical is more stable than your part b(ii) radical. Written explanation can be no more than one-two succinct sentence(s)!arrow_forward. 3°C with TH 12. (10pts total) Provide the major product for each reaction depicted below. If no reaction occurs write NR. Assume heat dissipation is carefully controlled in the fluorine reaction. 3H 24 total (30) 24 21 2h • 6H total ● 8H total 34 래 Br2 hv major product will be most Substituted 12 hv Br NR I too weak of a participate in P-1 F₂ hv Statistically most favored product will be major = most subst = thermo favored hydrogen atom abstractor to LL Farrow_forwardFive chemistry project topic that does not involve practicalarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningIntroductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
- Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
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: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry for Engineering Students
Chemistry
ISBN:9781337398909
Author:Lawrence S. Brown, Tom Holme
Publisher:Cengage Learning
Types of bonds; Author: Edspira;https://www.youtube.com/watch?v=Jj0V01Arebk;License: Standard YouTube License, CC-BY