ACHIEVE/CHEMICAL PRINCIPLES ACCESS 1TERM
7th Edition
ISBN: 9781319399849
Author: ATKINS
Publisher: MAC HIGHER
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 2, Problem 2B.1BST
Interpretation Introduction
Interpretation:
The Lewis structure of
Concept Introduction:
Lewis structures represent covalent bonds and describe valence electrons configuration of atoms. The covalent bonds are depicted by lines and unshared electron pairs by pairs of dots. The sequence to write Lewis structure of some molecule is given as follows:
- The central atom is identified and various other atoms are arranged around it. This central atom so chosen is often the least electronegative.
- Total valence electrons are estimated for each atoms.
- A single bond is first placed between each atom pair.
- The electrons left can be allocated as unshared electron pairs or as multiple bonds around
symbol of element to satisfy the octet (or duplet) for each atom.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Complete the following Lewis structures for the CICN molecule by adding dots for unshared
valence electrons and indicating formal charges. Evaluate the importance of each structure as a
contributor to a resonance hybrid. Cl – C = N, Cl = C – N, Cl = C = N
The structural formulas for ethanol, CH3CH2OH, and propene,
CH;CH=CH,2, are
нн
H
Н—С—С—0—н
H-C-C=C-H
нн
H H H
Ethanol
Propene
(a) Complete the Lewis structure for each molecule showing all valence
electrons.
(b) Using the VSEPR model, predict all bond angles in each molecule.
Complete the following Lewis structures for the HONS molecule by adding dots for unshared
valence electrons and indicating formal charges. Evaluate the importance of each structure as a
contributor to a resonance hybrid.
H – 0 – N = S, H–0 = N – S
Chapter 2 Solutions
ACHIEVE/CHEMICAL PRINCIPLES ACCESS 1TERM
Ch. 2 - Prob. 2A.1ASTCh. 2 - Prob. 2A.1BSTCh. 2 - Prob. 2A.2ASTCh. 2 - Prob. 2A.2BSTCh. 2 - Prob. 2A.3ASTCh. 2 - Prob. 2A.3BSTCh. 2 - Prob. 2A.4ASTCh. 2 - Prob. 2A.4BSTCh. 2 - Prob. 2A.1ECh. 2 - Prob. 2A.2E
Ch. 2 - Prob. 2A.3ECh. 2 - Prob. 2A.4ECh. 2 - Prob. 2A.5ECh. 2 - Prob. 2A.6ECh. 2 - Prob. 2A.7ECh. 2 - Prob. 2A.8ECh. 2 - Prob. 2A.9ECh. 2 - Prob. 2A.10ECh. 2 - Prob. 2A.11ECh. 2 - Prob. 2A.12ECh. 2 - Prob. 2A.13ECh. 2 - Prob. 2A.14ECh. 2 - Prob. 2A.15ECh. 2 - Prob. 2A.16ECh. 2 - Prob. 2A.17ECh. 2 - Prob. 2A.18ECh. 2 - Prob. 2A.19ECh. 2 - Prob. 2A.20ECh. 2 - Prob. 2A.21ECh. 2 - Prob. 2A.22ECh. 2 - Prob. 2A.23ECh. 2 - Prob. 2A.24ECh. 2 - Prob. 2A.25ECh. 2 - Prob. 2A.26ECh. 2 - Prob. 2A.27ECh. 2 - Prob. 2A.28ECh. 2 - Prob. 2A.29ECh. 2 - Prob. 2A.30ECh. 2 - Prob. 2B.1ASTCh. 2 - Prob. 2B.1BSTCh. 2 - Prob. 2B.2ASTCh. 2 - Prob. 2B.2BSTCh. 2 - Prob. 2B.3ASTCh. 2 - Prob. 2B.3BSTCh. 2 - Prob. 2B.4ASTCh. 2 - Prob. 2B.4BSTCh. 2 - Prob. 2B.5ASTCh. 2 - Prob. 2B.5BSTCh. 2 - Prob. 2B.1ECh. 2 - Prob. 2B.2ECh. 2 - Prob. 2B.3ECh. 2 - Prob. 2B.4ECh. 2 - Prob. 2B.5ECh. 2 - Prob. 2B.6ECh. 2 - Prob. 2B.7ECh. 2 - Prob. 2B.8ECh. 2 - Prob. 2B.9ECh. 2 - Prob. 2B.10ECh. 2 - Prob. 2B.11ECh. 2 - Prob. 2B.12ECh. 2 - Prob. 2B.13ECh. 2 - Prob. 2B.14ECh. 2 - Prob. 2B.15ECh. 2 - Prob. 2B.16ECh. 2 - Prob. 2B.17ECh. 2 - Prob. 2B.18ECh. 2 - Prob. 2B.19ECh. 2 - Prob. 2B.20ECh. 2 - Prob. 2B.21ECh. 2 - Prob. 2B.22ECh. 2 - Prob. 2B.23ECh. 2 - Prob. 2B.24ECh. 2 - Prob. 2C.1ASTCh. 2 - Prob. 2C.1BSTCh. 2 - Prob. 2C.2ASTCh. 2 - Prob. 2C.2BSTCh. 2 - Prob. 2C.3ASTCh. 2 - Prob. 2C.3BSTCh. 2 - Prob. 2C.1ECh. 2 - Prob. 2C.2ECh. 2 - Prob. 2C.3ECh. 2 - Prob. 2C.4ECh. 2 - Prob. 2C.5ECh. 2 - Prob. 2C.6ECh. 2 - Prob. 2C.7ECh. 2 - Prob. 2C.8ECh. 2 - Prob. 2C.9ECh. 2 - Prob. 2C.10ECh. 2 - Prob. 2C.11ECh. 2 - Prob. 2C.12ECh. 2 - Prob. 2C.13ECh. 2 - Prob. 2C.14ECh. 2 - Prob. 2C.15ECh. 2 - Prob. 2C.16ECh. 2 - Prob. 2C.17ECh. 2 - Prob. 2C.18ECh. 2 - Prob. 2D.1ASTCh. 2 - Prob. 2D.1BSTCh. 2 - Prob. 2D.2ASTCh. 2 - Prob. 2D.2BSTCh. 2 - Prob. 2D.1ECh. 2 - Prob. 2D.2ECh. 2 - Prob. 2D.3ECh. 2 - Prob. 2D.4ECh. 2 - Prob. 2D.5ECh. 2 - Prob. 2D.6ECh. 2 - Prob. 2D.7ECh. 2 - Prob. 2D.8ECh. 2 - Prob. 2D.9ECh. 2 - Prob. 2D.10ECh. 2 - Prob. 2D.11ECh. 2 - Prob. 2D.12ECh. 2 - Prob. 2D.13ECh. 2 - Prob. 2D.14ECh. 2 - Prob. 2D.15ECh. 2 - Prob. 2D.16ECh. 2 - Prob. 2D.17ECh. 2 - Prob. 2D.18ECh. 2 - Prob. 2D.19ECh. 2 - Prob. 2D.20ECh. 2 - Prob. 2E.1ASTCh. 2 - Prob. 2E.1BSTCh. 2 - Prob. 2E.2ASTCh. 2 - Prob. 2E.2BSTCh. 2 - Prob. 2E.3ASTCh. 2 - Prob. 2E.3BSTCh. 2 - Prob. 2E.4ASTCh. 2 - Prob. 2E.4BSTCh. 2 - Prob. 2E.5ASTCh. 2 - Prob. 2E.5BSTCh. 2 - Prob. 2E.1ECh. 2 - Prob. 2E.2ECh. 2 - Prob. 2E.3ECh. 2 - Prob. 2E.4ECh. 2 - Prob. 2E.5ECh. 2 - Prob. 2E.6ECh. 2 - Prob. 2E.7ECh. 2 - Prob. 2E.8ECh. 2 - Prob. 2E.9ECh. 2 - Prob. 2E.10ECh. 2 - Prob. 2E.11ECh. 2 - Prob. 2E.12ECh. 2 - Prob. 2E.13ECh. 2 - Prob. 2E.14ECh. 2 - Prob. 2E.15ECh. 2 - Prob. 2E.16ECh. 2 - Prob. 2E.17ECh. 2 - Prob. 2E.18ECh. 2 - Prob. 2E.19ECh. 2 - Prob. 2E.20ECh. 2 - Prob. 2E.21ECh. 2 - Prob. 2E.22ECh. 2 - Prob. 2E.23ECh. 2 - Prob. 2E.24ECh. 2 - Prob. 2E.25ECh. 2 - Prob. 2E.26ECh. 2 - Prob. 2E.27ECh. 2 - Prob. 2E.28ECh. 2 - Prob. 2E.29ECh. 2 - Prob. 2E.30ECh. 2 - Prob. 2F.1ASTCh. 2 - Prob. 2F.1BSTCh. 2 - Prob. 2F.2ASTCh. 2 - Prob. 2F.2BSTCh. 2 - Prob. 2F.3ASTCh. 2 - Prob. 2F.3BSTCh. 2 - Prob. 2F.4ASTCh. 2 - Prob. 2F.4BSTCh. 2 - Prob. 2F.1ECh. 2 - Prob. 2F.2ECh. 2 - Prob. 2F.3ECh. 2 - Prob. 2F.4ECh. 2 - Prob. 2F.5ECh. 2 - Prob. 2F.6ECh. 2 - Prob. 2F.7ECh. 2 - Prob. 2F.8ECh. 2 - Prob. 2F.9ECh. 2 - Prob. 2F.10ECh. 2 - Prob. 2F.11ECh. 2 - Prob. 2F.12ECh. 2 - Prob. 2F.13ECh. 2 - Prob. 2F.14ECh. 2 - Prob. 2F.15ECh. 2 - Prob. 2F.16ECh. 2 - Prob. 2F.17ECh. 2 - Prob. 2F.18ECh. 2 - Prob. 2F.19ECh. 2 - Prob. 2F.20ECh. 2 - Prob. 2F.21ECh. 2 - Prob. 2G.1ASTCh. 2 - Prob. 2G.1BSTCh. 2 - Prob. 2G.2ASTCh. 2 - Prob. 2G.2BSTCh. 2 - Prob. 2G.1ECh. 2 - Prob. 2G.2ECh. 2 - Prob. 2G.3ECh. 2 - Prob. 2G.4ECh. 2 - Prob. 2G.5ECh. 2 - Prob. 2G.6ECh. 2 - Prob. 2G.7ECh. 2 - Prob. 2G.8ECh. 2 - Prob. 2G.9ECh. 2 - Prob. 2G.11ECh. 2 - Prob. 2G.12ECh. 2 - Prob. 2G.13ECh. 2 - Prob. 2G.14ECh. 2 - Prob. 2G.15ECh. 2 - Prob. 2G.16ECh. 2 - Prob. 2G.17ECh. 2 - Prob. 2G.18ECh. 2 - Prob. 2G.19ECh. 2 - Prob. 2G.20ECh. 2 - Prob. 2G.21ECh. 2 - Prob. 2G.22ECh. 2 - Prob. 2.1ECh. 2 - Prob. 2.2ECh. 2 - Prob. 2.3ECh. 2 - Prob. 2.4ECh. 2 - Prob. 2.5ECh. 2 - Prob. 2.6ECh. 2 - Prob. 2.7ECh. 2 - Prob. 2.8ECh. 2 - Prob. 2.9ECh. 2 - Prob. 2.10ECh. 2 - Prob. 2.11ECh. 2 - Prob. 2.12ECh. 2 - Prob. 2.13ECh. 2 - Prob. 2.14ECh. 2 - Prob. 2.17ECh. 2 - Prob. 2.19ECh. 2 - Prob. 2.22ECh. 2 - Prob. 2.23ECh. 2 - Prob. 2.24ECh. 2 - Prob. 2.25ECh. 2 - Prob. 2.26ECh. 2 - Prob. 2.27ECh. 2 - Prob. 2.28ECh. 2 - Prob. 2.29ECh. 2 - Prob. 2.30ECh. 2 - Prob. 2.31ECh. 2 - Prob. 2.32ECh. 2 - Prob. 2.33ECh. 2 - Prob. 2.34ECh. 2 - Prob. 2.35ECh. 2 - Prob. 2.36ECh. 2 - Prob. 2.37ECh. 2 - Prob. 2.39ECh. 2 - Prob. 2.40ECh. 2 - Prob. 2.41ECh. 2 - Prob. 2.42ECh. 2 - Prob. 2.43ECh. 2 - Prob. 2.44ECh. 2 - Prob. 2.45ECh. 2 - Prob. 2.46ECh. 2 - Prob. 2.47ECh. 2 - Prob. 2.48ECh. 2 - Prob. 2.49ECh. 2 - Prob. 2.50ECh. 2 - Prob. 2.51ECh. 2 - Prob. 2.52ECh. 2 - Prob. 2.53ECh. 2 - Prob. 2.54ECh. 2 - Prob. 2.55ECh. 2 - Prob. 2.56ECh. 2 - Prob. 2.57ECh. 2 - Prob. 2.58ECh. 2 - Prob. 2.59ECh. 2 - Prob. 2.60ECh. 2 - Prob. 2.61ECh. 2 - Prob. 2.62ECh. 2 - Prob. 2.63ECh. 2 - Prob. 2.64E
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
- Draw the Lewis structure for monochloramine, which is a covalent compound with the formula NH2Cl. Include all nonbonding electrons, such as lone pairs, and any nonzero formal charges. Draw the Lewis structure for hydrazine, which has the formula N2H4. Include all nonbonding electrons, such as lone pairs, and any nonzero formal charges.arrow_forwardcarbon tetrachloride was formerly used in fire extinguishers for electrical fires.it is no longer used for this purpose because of the formation of the toxic gas phosgene,CL2CO.wRITE THE LEWIS STRUCTURES for the methane and ethane molecules.arrow_forwardDoes your molecular exhibit resonance? If so, show all possible forms. Does your molecule have any isomers? If so, show Lewis structures of them as well. for CH3CH2OHarrow_forward
- Unshared, or lone, electron pairs play an important role in determining the chemical and physical properties of organic compounds. Thus, it is important to know which atoms carry unshared pairs. Use the structural formulas below to determine the number of unshared pairs at each designated atom. Be sure your answers are consistent with the formal charges on the formulas. CH3 CH₂ CH3 a H₂C C-C C The number of unshared pairs at atom a is | The number of unshared pairs at atom b is The number of unshared pairs at atom c is | -H The number of unshared pairs at atom a is The number of unshared pairs at atom b is The number of unshared pairs at atom c is | Submit Answer Retry Entire Group 1 more group attempt remainingarrow_forwardAlthough carbon has four bonds in stable molecules, sometimes reactive carbon intermediates that contain carbon atoms without four bonds are formed for very short time periods. Examples of these unstable intermediates include the methyl carbocation (CH 3) + and the methyl carbanion (CH 3) −. Draw Lewis structures for both unstable ions and predict the shape around carbon.arrow_forwardWrite a Lewis structure for the amide ion, NH2─, and assign formal charges to each atom.arrow_forward
- Unshared, or lone, electron pairs play an important role in determining the chemical and physical properties of organic compounds. Thus, it is important to know which atoms carry unshared pairs. Use the structural formulas below to determine the number of unshared pairs at each designated atom. Be sure your answers are consistent with the formal charges on the formulas. The number of unshared pairs at atom a is 4 The number of unshared pairs at atom b is 2 H The number of unshared pairs at atom c is 3 The number of unshared pairs at atom a is The number of unshared pairs at atom b is C-NEN а b H The number of unshared pairs at atom c is Submit Answer Retry Entire Group 8 more group attempts remainingarrow_forwardDetermine the number of valence electrons in (CH₃C(O)CN) and then draw the corresponding Lewis structure.arrow_forwardA compound has the formula C8H8 and does not contain any double or triple bonds. All the carbon atoms are chemically ideitical, as are all the hydrogen atoms. Draw the Lewis structure for this molecule.arrow_forward
- Which of the following bonds are polar: (a) P—O; (b) S—F; (c) Br—Br; (d) O—Cl? Which is the more electronegative atom in each polar bond?arrow_forwardThe following is a skeleton of a molecular anion having the overall formula C7H6NO–. The H atoms are not shown. Starting with the structure drawn below, complete the Lewis structure by adding all H atoms, valence electrons, and π bonds. This structure will have a –1 formal charge on the oxygen.arrow_forwardIn the molecular compound CH2O, how many lone pairs are around oxygen?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
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
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