Chemistry: The Central Science (14th Edition)
14th Edition
ISBN: 9780134554563
Author: Brown
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 8, Problem 33E
Using Lewis symbols and Lewis structures, diagram the formation of SiCl4from Si and CI atoms, showing valence-shell electrons.
- How many valence electrons does Si have initially?
- How many valence electrons does each Cl have initially?
- How many valence electrons surround the Si in the SiCl4 molecule?
- How many valence electrons surround each Cl in the SiCl4 molecule?
- How many bonding pairs of electrons are in the SiCl4 molecule?
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
13. (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.← Cleavage
2°C. +
Bond C
+3°C•
CH3 2C
Cleavage
E
2°C. 26.
weakest bond
Intact molecule
Strongest 3°C 20.
Gund
Largest
argest
a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in
appropriate boxes.
C
Weakest
bond
A
Produces
Most
Bond
Strongest
Bond
Strongest Gund
produces least stable
radicals
Weakest
Stable radical
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.
13°C. formed in
bound C
cleavage
ii. Which ONE cleavage product is the least stable? A condensed or bond line
representation is fine.
• CH3
methyl radical
Formed in Gund A Cleavage
c.…
Br.
COOH Br,
FCH COOH E
FeBr
ASOCI
B
NH
(CH,CO),OD Br₂
2
C
alcKOH
Find A to F (all)
Chapter 8 Solutions
Chemistry: The Central Science (14th Edition)
Ch. 8.2 - Which of the these elements is most likely to from...Ch. 8.2 - Prob. 8.1.2PECh. 8.2 - Which of the following bond is the most polar? H-F...Ch. 8.2 - Prob. 8.2.2PECh. 8.3 - Prob. 8.3.1PECh. 8.3 - Prob. 8.3.2PECh. 8.4 - Which of the following bonds is the most polar? a....Ch. 8.4 - Which of the following bonds is most polar: S-Cl,...Ch. 8.4 - Prob. 8.5.1PECh. 8.4 - The dipole moment of chlorine monofluoride,...
Ch. 8.5 - Which of the these molecules has a Lewis structure...Ch. 8.5 -
How many valence electrons should appear in the...Ch. 8.5 - Compare the lewis symbol for neon the structure...Ch. 8.5 - Prob. 8.7.2PECh. 8.5 - Prob. 8.8.1PECh. 8.5 - Prob. 8.8.2PECh. 8.5 - Prob. 8.9.1PECh. 8.5 - Prob. 8.9.2PECh. 8.6 - Which of the statements about resonance is true?...Ch. 8.6 - Prob. 8.10.2PECh. 8.7 - Prob. 8.11.1PECh. 8.7 - Prob. 8.11.2PECh. 8 - Prob. 1DECh. 8 - Prob. 1ECh. 8 - Prob. 2ECh. 8 - A portion of a two-dimensional "slab" of NaCl(s)...Ch. 8 - Prob. 4ECh. 8 - Prob. 5ECh. 8 - Incomplete Lewis structures for the nitrous acid...Ch. 8 - Prob. 7ECh. 8 - Prob. 8ECh. 8 - Prob. 9ECh. 8 - True or false: The hydrogen atom is most stable...Ch. 8 - Consider the element silicon, Si. Write its...Ch. 8 - Write the electron configuration for the element...Ch. 8 - Prob. 13ECh. 8 - What is the Lewis symbol for each of the following...Ch. 8 - Using Lewis symbols, diagram the reaction between...Ch. 8 - Use Lewis symbols to represent the reaction that...Ch. 8 - Predict the chemical formula of the ionic compound...Ch. 8 - Prob. 18ECh. 8 - Prob. 19ECh. 8 - Prob. 20ECh. 8 - Is lattice energy usually endothermic or...Ch. 8 - NaCI and KF have the same crystal structure. The...Ch. 8 - Prob. 23ECh. 8 - Prob. 24ECh. 8 - Consider the ionic compounds KF, NaCl, NaBr, and...Ch. 8 - Which of the following trends in lattice energy is...Ch. 8 - Energy is required to remove two electrons from Ca...Ch. 8 - Prob. 28ECh. 8 - Use data from Appendix C, Figure 7.10, and Figure...Ch. 8 - Prob. 30ECh. 8 - Prob. 31ECh. 8 - Prob. 32ECh. 8 - Using Lewis symbols and Lewis structures, diagram...Ch. 8 - Use Lewis symbols and Lewis structures to diagram...Ch. 8 - Prob. 35ECh. 8 - Prob. 36ECh. 8 - Prob. 37ECh. 8 - What is the trend in electronegativity going from...Ch. 8 - Prob. 39ECh. 8 - By referring only to the periodic table, select...Ch. 8 - which of the following bonds are polar? B-F,...Ch. 8 - Arrange the bonds in each of the following sets in...Ch. 8 - Prob. 43ECh. 8 - Prob. 44ECh. 8 - In the following pairs of binary compounds,...Ch. 8 - Prob. 46ECh. 8 - Prob. 47ECh. 8 - Write Lewis structures for the following: H2CO...Ch. 8 - Prob. 49ECh. 8 - Draw the dominant Lewis structure for the...Ch. 8 - Write Lewis structures that obey the octet rule...Ch. 8 - Prob. 52ECh. 8 - Prob. 53ECh. 8 - Prob. 54ECh. 8 - Prob. 55ECh. 8 - Prob. 56ECh. 8 - Prob. 57ECh. 8 - Prob. 58ECh. 8 - Prob. 59ECh. 8 - Prob. 60ECh. 8 - Prob. 61ECh. 8 - 8.62 For Group 3A-7A elements in the third row of...Ch. 8 - Draw the Lewis structures for each of the...Ch. 8 - Prob. 64ECh. 8 - In the vapor phase, BeCl2exists as a discrete...Ch. 8 -
8.66
Describe the molecule xenon trioxide, XeO3,...Ch. 8 -
8.67 There are many Lewis structures you could...Ch. 8 - Prob. 68ECh. 8 - Using Table 8.3, estimate H for each of the...Ch. 8 - Using Table 8.3, estimate H for the following...Ch. 8 - State whether each of these statements is true or...Ch. 8 - Prob. 72ECh. 8 - Prob. 73ECh. 8 - Prob. 74ECh. 8 - Prob. 75ECh. 8 - Prob. 76ECh. 8 - A new compound is made that has a C-C bond length...Ch. 8 - A new compound is made that has an N-N bond length...Ch. 8 - Prob. 79AECh. 8 - Prob. 80AECh. 8 - An ionic substance of formula MX has a lattice...Ch. 8 - Prob. 82AECh. 8 - Prob. 83AECh. 8 - Prob. 84AECh. 8 - Consider the collection of nonmetallic elements 0,...Ch. 8 - The substance chlorine monoxide, CIO(g), is...Ch. 8 -
[8.87]
a. using the electronegativities of Br...Ch. 8 - Prob. 88AECh. 8 - Although I3- is a known ion, F3- is not. a. Draw...Ch. 8 - Calculate the formal charge on the indicated atom...Ch. 8 - The hypochlorite ion, CIO- , is the active...Ch. 8 - Prob. 92AECh. 8 - a. Triazine, C3 H3N3, is like benzene except that...Ch. 8 - Prob. 94IECh. 8 - Prob. 95IECh. 8 - Prob. 96IECh. 8 - Prob. 97IECh. 8 - Prob. 98IECh. 8 - Prob. 99IECh. 8 - Prob. 100IECh. 8 - Prob. 101IECh. 8 - Prob. 102IECh. 8 -
8.103 The compound chloral hydrate, known in...Ch. 8 - Barium azide is 62.04% Ba and 37.96% N. Each azide...Ch. 8 - Acetylene (C2H2) and nitrogen (N2) both contain a...Ch. 8 - Prob. 106IECh. 8 - Prob. 107IECh. 8 -
8.108 Formic acid has the chemical formula...Ch. 8 - Prob. 109IECh. 8 - Prob. 110IE
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
- Show work. don't give Ai generated solutionarrow_forwardHi!! 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!!arrow_forwardHi!! 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!!arrow_forward
- . (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 Cleavagearrow_forwardWhich carbocation is more stable?arrow_forwardAre the products of the given reaction correct? Why or why not?arrow_forward
- The 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_forwardMy 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_forward
- A 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_forwardIn statistical thermodynamics, check the hcv following equality: ß Aɛ = KTarrow_forwardPlease correct answer and don't used hand raitingarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- General Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage LearningIntroductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
General Chemistry - Standalone book (MindTap Cour...
Chemistry
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Cengage Learning
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
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
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Types of bonds; Author: Edspira;https://www.youtube.com/watch?v=Jj0V01Arebk;License: Standard YouTube License, CC-BY