EBK FOUNDATIONS OF COLLEGE CHEMISTRY
EBK FOUNDATIONS OF COLLEGE CHEMISTRY
15th Edition
ISBN: 9781118930144
Author: Willard
Publisher: JOHN WILEY+SONS INC.
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 11, Problem 84AE
Interpretation Introduction

Interpretation:

The reason for which fluorine is given importance in terms of electronegativity and what combination of atoms on periodic table form the ionic bond have to be identified.

Concept Introduction:

Lewis structure:

The representation of valence shell electrons around the atom is known as Lewis structure or Lewis dot structure.  Electrons are represented as a dot in Lewis structures, a single dot represents unpaired electron and paired of dots represents paired electrons.

Expert Solution & Answer
Check Mark

Explanation of Solution

Given,

The mass of sulfur is 1.40g.

The mass of oxygen is 2.10g.

The empirical formula can be calculated as follows:

SOMass1.40g2.10gMolarmass32.065g/mol16.0g/molMoles=massMolarmass1.40g32.065g/mol2.10g16.0g/mol0.0437mol0.131molDivideby0.0437mol0.0437mol0.0437mol0.131mol0.0437mol13.00

The empirical formula of the compound is SO3.

The Lewis structure of SO3 is drawn as follows:

The total number of valence electrons in SO3 is 24. 6 valence electrons from sulfur atom and 6 from each O atom.

The three oxygen atoms are bonded to central sulfur atom. Write skeletal structure representing this and place two electrons between each sulfur and oxygen atom.

EBK FOUNDATIONS OF COLLEGE CHEMISTRY, Chapter 11, Problem 84AE , additional homework tip  1

Here 6 valence electrons are used and 18 valence electrons are remaining. These electrons can be distributed over oxygen and sulfur atoms to get an octet configuration.

EBK FOUNDATIONS OF COLLEGE CHEMISTRY, Chapter 11, Problem 84AE , additional homework tip  2EBK FOUNDATIONS OF COLLEGE CHEMISTRY, Chapter 11, Problem 84AE , additional homework tip  3

Here one of the oxygen atom is electron deficient, so one electron pair is given to oxygen from sulfur. Therefore, Lewis structure of SO3 may be represented as follows:

EBK FOUNDATIONS OF COLLEGE CHEMISTRY, Chapter 11, Problem 84AE , additional homework tip  4

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Protecting Groups and Carbonyls 6) The synthesis generates allethrolone that exhibits high insect toxicity but low mammalian toxicity. They are used in pet shampoo, human lice shampoo, and industrial sprays for insects and mosquitos. Propose detailed mechanistic steps to generate the allethrolone label the different types of reagents (Grignard, acid/base protonation, acid/base deprotonation, reduction, oxidation, witting, aldol condensation, Robinson annulation, etc.) III + VI HS HS H+ CH,CH,Li III I II IV CI + P(Ph)3 V ༼ Hint: no strong base added VI S VII IX HO VIII -MgBr HgCl2,HgO HO. isomerization aqeuous solution H,SO, ༽༽༤༽༽ X MeOH Hint: enhances selectivity for reaction at the S X ☑
Draw the complete mechanism for the acid-catalyzed hydration of this alkene. esc 田 Explanation Check 1 888 Q A slock Add/Remove step Q F4 F5 F6 A བྲA F7 $ % 5 @ 4 2 3 & 6 87 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Ce W E R T Y U S D LL G H IK DD 요 F8 F9 F10 F1 * ( 8 9 0 O P J K L Z X C V B N M H He command
Explanation Check F1 H₂O H₂ Pd 1) MCPBA 2) H3O+ 1) Hg(OAc)2, H₂O 2) NaBH4 OH CI OH OH OH hydration halohydrin formation addition halogenation hydrogenation inhalation hydrogenation hydration ☐ halohydrin formation addition halogenation formation chelation hydrogenation halohydrin formation substitution hydration halogenation addition Ohalohydrin formation subtraction halogenation addition hydrogenation hydration F2 80 F3 σ F4 F5 F6 1 ! 2 # 3 $ 4 % 05 Q W & Å © 2025 McGraw Hill LLC. All Rights Reserved. F7 F8 ( 6 7 8 9 LU E R T Y U A F9

Chapter 11 Solutions

EBK FOUNDATIONS OF COLLEGE CHEMISTRY

Ch. 11.9 - Prob. 11.11PCh. 11.10 - Prob. 11.12PCh. 11 - Prob. 1RQCh. 11 - Prob. 2RQCh. 11 - Prob. 3RQCh. 11 - Prob. 4RQCh. 11 - Prob. 5RQCh. 11 - Prob. 6RQCh. 11 - Prob. 7RQCh. 11 - Prob. 8RQCh. 11 - Prob. 9RQCh. 11 - Prob. 10RQCh. 11 - Prob. 11RQCh. 11 - Prob. 12RQCh. 11 - Prob. 13RQCh. 11 - Prob. 14RQCh. 11 - Prob. 15RQCh. 11 - Prob. 16RQCh. 11 - Prob. 17RQCh. 11 - Prob. 18RQCh. 11 - Prob. 19RQCh. 11 - Prob. 20RQCh. 11 - Prob. 21RQCh. 11 - Prob. 22RQCh. 11 - Prob. 23RQCh. 11 - Prob. 24RQCh. 11 - Prob. 25RQCh. 11 - Prob. 26RQCh. 11 - Prob. 28RQCh. 11 - Prob. 30RQCh. 11 - Prob. 31RQCh. 11 - Prob. 33RQCh. 11 - Prob. 36RQCh. 11 - Prob. 1PECh. 11 - Prob. 2PECh. 11 - Prob. 3PECh. 11 - Prob. 4PECh. 11 - Prob. 5PECh. 11 - Prob. 6PECh. 11 - Prob. 7PECh. 11 - Prob. 8PECh. 11 - Prob. 9PECh. 11 - Prob. 10PECh. 11 - Prob. 11PECh. 11 - Prob. 12PECh. 11 - Prob. 13PECh. 11 - Prob. 14PECh. 11 - Prob. 15PECh. 11 - Prob. 16PECh. 11 - Prob. 17PECh. 11 - Prob. 18PECh. 11 - Prob. 19PECh. 11 - Prob. 20PECh. 11 - Prob. 21PECh. 11 - Prob. 22PECh. 11 - Prob. 23PECh. 11 - Prob. 24PECh. 11 - Prob. 25PECh. 11 - Prob. 26PECh. 11 - Prob. 27PECh. 11 - Prob. 28PECh. 11 - Prob. 29PECh. 11 - Prob. 30PECh. 11 - Prob. 31PECh. 11 - Prob. 32PECh. 11 - Prob. 33PECh. 11 - Prob. 34PECh. 11 - Prob. 35PECh. 11 - Prob. 36PECh. 11 - Prob. 37PECh. 11 - Prob. 38PECh. 11 - Prob. 39PECh. 11 - Prob. 40PECh. 11 - Prob. 47PECh. 11 - Prob. 48PECh. 11 - Prob. 49PECh. 11 - Prob. 50PECh. 11 - Prob. 51PECh. 11 - Prob. 52PECh. 11 - Prob. 55AECh. 11 - Prob. 56AECh. 11 - Prob. 57AECh. 11 - Prob. 58AECh. 11 - Prob. 59AECh. 11 - Prob. 63AECh. 11 - Prob. 64AECh. 11 - Prob. 65AECh. 11 - Prob. 66AECh. 11 - Prob. 67AECh. 11 - Prob. 68AECh. 11 - Prob. 76AECh. 11 - Prob. 77AECh. 11 - Prob. 78AECh. 11 - Prob. 81AECh. 11 - Prob. 82AECh. 11 - Prob. 83AECh. 11 - Prob. 84AECh. 11 - Prob. 85AECh. 11 - Prob. 86AECh. 11 - Prob. 87AECh. 11 - Prob. 88CECh. 11 - Prob. 89CECh. 11 - Prob. 90CECh. 11 - Prob. 92CECh. 11 - Prob. 93CECh. 11 - Prob. 94CECh. 11 - Prob. 95CE
Knowledge Booster
Background pattern image
Chemistry
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
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Text book image
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
Text book image
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Text book image
Introductory Chemistry For Today
Chemistry
ISBN:9781285644561
Author:Seager
Publisher:Cengage
Text book image
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:9781938168390
Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:OpenStax
Text book image
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
Stoichiometry - Chemistry for Massive Creatures: Crash Course Chemistry #6; Author: Crash Course;https://www.youtube.com/watch?v=UL1jmJaUkaQ;License: Standard YouTube License, CC-BY
Bonding (Ionic, Covalent & Metallic) - GCSE Chemistry; Author: Science Shorts;https://www.youtube.com/watch?v=p9MA6Od-zBA;License: Standard YouTube License, CC-BY
General Chemistry 1A. Lecture 12. Two Theories of Bonding.; Author: UCI Open;https://www.youtube.com/watch?v=dLTlL9Z1bh0;License: CC-BY