OWLV2 FOR MOORE/STANITSKI'S CHEMISTRY:
5th Edition
ISBN: 9781285460369
Author: STANITSKI
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 10, Problem 118QRT
(a)
Interpretation Introduction
Interpretation:
The Lewis structure for the given compound,
Concept Introduction:
Lewis dot structure of a molecule is the structural representation in which bonded atoms of a molecule are shown along with the lone pair of electrons present on them. The valence electrons around an atom are shown by dots. Bonds between atoms are shown by lines and the lone pair of electrons is shown by a pair of dots.
(b)
Interpretation Introduction
Interpretation:
Two resonance structures for this molecule have to be drawn.
Concept Introduction:
Resonance is the phenomena of the delocalization of pi electrons to give extra stability to the molecule. This extra stability comes from the distribution of the energy of the molecule in the resonance structures formed.
(c)
Interpretation Introduction
Interpretation:
The VSEPR theory has to be used to predict the geometry around each carbon and nitrogen atom in the resonance structures.
Concept Introduction:
The three dimensional arrangement of atoms possesses by the molecule in space is known as the molecular geometry. The molecular geometry of any molecule is identified by using the central metal atom, pair of electrons and atoms surrounding the central atom with the help of VSEPR theory. The shape in VSEPR model gives specific angles between the bonds for the corresponding shape and these angles are known as bond angles.
(d)
Interpretation Introduction
Interpretation:
The correct prediction in part (c) has to be detected.
Concept Introduction:
The hybridization is the process of combining atomic orbitals together to get the appropriate directional properties and improved overlapping of atomic orbitals. A hybrid orbital is formed by the mixing of orbital.
(e)
Interpretation Introduction
Interpretation:
The hybridization of nitrogen atom has to be described.
Concept Introduction:
The hybridization is the process of combining atomic orbitals together to get the appropriate directional properties and improved overlapping of atomic orbitals. A hybrid orbital is formed by the mixing of orbital.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
For each of the following covalent bonds: (a) use the symbols δ+ and δ- to indicate the direction of polarity (if any).(a) C-F; (b) N-Br; (c) B-C; (d) Si-H(b) Rank the following covalent bonds in order of increasing polarity. (i) C-H, O-H, N-H; (ii) C-N, C-O, B-O; (iii) C-P, C-S, C-N
Chemistry
(a) Write three more resonance structures for each of compounds 1 and 2. (b) In each of compounds 1 and 2, determine which resonance structure contributes the most and explain your answer. (c) Are the 3/4 structures resonance structures or different compounds? Same question for 5/6 structures. Explain your answers.
Draw the molecules in Problem 1.61 using line structures
Chapter 10 Solutions
OWLV2 FOR MOORE/STANITSKI'S CHEMISTRY:
Ch. 10.1 - Heptane, C7H16, can be catalytically reformed to...Ch. 10.1 - Prob. 10.2ECh. 10.1 - Prob. 10.1PSPCh. 10.1 - Prob. 10.3ECh. 10.2 - Prob. 10.4ECh. 10.4 - Using a table of average bond enthalpies. Table...Ch. 10.4 - Prob. 10.5CECh. 10.4 - Prob. 10.6CECh. 10.4 - Prob. 10.7CECh. 10.4 - Prob. 10.3PSP
Ch. 10.4 - Prob. 10.8CECh. 10.4 - Prob. 10.9CECh. 10.4 - Prob. 10.10CECh. 10.4 - Prob. 10.11ECh. 10.5 - Prob. 10.12ECh. 10.5 - Prob. 10.4PSPCh. 10.5 - Prob. 10.13ECh. 10.6 - Prob. 10.14CECh. 10.6 - Prob. 10.5PSPCh. 10.6 - Prob. 10.6PSPCh. 10.6 - Prob. 10.7PSPCh. 10.6 - Prob. 10.8PSPCh. 10.6 - Prob. 10.9PSPCh. 10.6 - Prob. 10.15CECh. 10.6 - Prob. 10.16ECh. 10.7 - Prob. 10.17CECh. 10.7 - Prob. 10.18CECh. 10.7 - Prob. 10.19CECh. 10.7 - Prob. 10.20CECh. 10.7 - Prob. 10.10PSPCh. 10.7 - Prob. 10.21ECh. 10 - Prob. ISPCh. 10 - Prob. IISPCh. 10 - Prob. IIISPCh. 10 - Prob. 1QRTCh. 10 - Prob. 2QRTCh. 10 - Prob. 3QRTCh. 10 - Prob. 4QRTCh. 10 - Prob. 5QRTCh. 10 - Prob. 6QRTCh. 10 - Prob. 7QRTCh. 10 - Give two reasons why ethylene glycol has a higher...Ch. 10 - Prob. 9QRTCh. 10 - Prob. 10QRTCh. 10 - Prob. 11QRTCh. 10 - Prob. 12QRTCh. 10 - Prob. 13QRTCh. 10 - Prob. 14QRTCh. 10 - Prob. 15QRTCh. 10 - Prob. 16QRTCh. 10 - Prob. 17QRTCh. 10 - Prob. 18QRTCh. 10 - Prob. 19QRTCh. 10 - Prob. 20QRTCh. 10 - Prob. 21QRTCh. 10 - Prob. 22QRTCh. 10 - Prob. 23QRTCh. 10 - Prob. 24QRTCh. 10 - Prob. 25QRTCh. 10 - Prob. 26QRTCh. 10 - Prob. 27QRTCh. 10 - Prob. 28QRTCh. 10 - Prob. 29QRTCh. 10 - Prob. 30QRTCh. 10 - Prob. 31QRTCh. 10 - Prob. 32QRTCh. 10 - Prob. 33QRTCh. 10 - Prob. 34QRTCh. 10 - Prob. 35QRTCh. 10 - Prob. 36QRTCh. 10 - Prob. 37QRTCh. 10 - Prob. 38QRTCh. 10 - Prob. 39QRTCh. 10 - Prob. 40QRTCh. 10 - Prob. 41QRTCh. 10 - Prob. 42QRTCh. 10 - Prob. 43QRTCh. 10 - Prob. 44QRTCh. 10 - Prob. 45QRTCh. 10 - Prob. 46QRTCh. 10 - Prob. 47QRTCh. 10 - Beeswax contains this compound:
Identify what...Ch. 10 - Prob. 49QRTCh. 10 - Prob. 50QRTCh. 10 - Prob. 51QRTCh. 10 - Prob. 52QRTCh. 10 - Prob. 53QRTCh. 10 - Prob. 54QRTCh. 10 - Prob. 55QRTCh. 10 - Prob. 56QRTCh. 10 - Prob. 57QRTCh. 10 - Prob. 58QRTCh. 10 - Prob. 59QRTCh. 10 - Prob. 60QRTCh. 10 - Prob. 61QRTCh. 10 - Prob. 62QRTCh. 10 - Prob. 63QRTCh. 10 - Prob. 64QRTCh. 10 - Prob. 65QRTCh. 10 - Prob. 66QRTCh. 10 - Prob. 67QRTCh. 10 - Prob. 68QRTCh. 10 - Prob. 69QRTCh. 10 - Prob. 70QRTCh. 10 - Prob. 71QRTCh. 10 - Prob. 72QRTCh. 10 - Prob. 73QRTCh. 10 - Prob. 74QRTCh. 10 - Prob. 75QRTCh. 10 - Prob. 76QRTCh. 10 - Prob. 77QRTCh. 10 - Prob. 78QRTCh. 10 - Prob. 79QRTCh. 10 -
Identify and name all the functional groups in...Ch. 10 - Prob. 81QRTCh. 10 - Prob. 82QRTCh. 10 - Prob. 83QRTCh. 10 - Prob. 84QRTCh. 10 - Prob. 85QRTCh. 10 - Prob. 86QRTCh. 10 - Prob. 87QRTCh. 10 - Prob. 88QRTCh. 10 - Prob. 89QRTCh. 10 - Prob. 90QRTCh. 10 - Prob. 91QRTCh. 10 - Prob. 92QRTCh. 10 - Prob. 93QRTCh. 10 - Prob. 94QRTCh. 10 - Prob. 95QRTCh. 10 - Prob. 96QRTCh. 10 - Assume that a car burns pure octane. C8H18 (d =...Ch. 10 - Prob. 98QRTCh. 10 - Prob. 99QRTCh. 10 - Prob. 100QRTCh. 10 - Prob. 101QRTCh. 10 - Prob. 102QRTCh. 10 - Prob. 103QRTCh. 10 - Prob. 104QRTCh. 10 - Prob. 105QRTCh. 10 - Prob. 106QRTCh. 10 - Prob. 107QRTCh. 10 - Prob. 108QRTCh. 10 - Prob. 109QRTCh. 10 - Prob. 110QRTCh. 10 - Prob. 111QRTCh. 10 - Prob. 112QRTCh. 10 - Prob. 113QRTCh. 10 - Prob. 114QRTCh. 10 - Prob. 115QRTCh. 10 - Prob. 116QRTCh. 10 - Prob. 118QRTCh. 10 - Prob. 119QRTCh. 10 - Prob. 120QRTCh. 10 - Prob. 121QRTCh. 10 - Prob. 122QRTCh. 10 - Prob. 123QRTCh. 10 - Prob. 124QRTCh. 10 - Prob. 125QRTCh. 10 - Prob. 126QRTCh. 10 - Prob. 127QRTCh. 10 - Prob. 10.ACPCh. 10 - Prob. 10.BCPCh. 10 - Prob. 10.CCP
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 Lewis structures for the following compounds. Remember to enclose ions in square brackets. On your answer sheet, state the number of valence electrons in each compound. (a) NaCN (b) CH 3 Br (c) Ca(OCl) 2arrow_forwardThe arrangement of atoms in several biologically important molecules is given here. Complete the Lewis structures of these molecules by adding multiple bonds and lone pairs. Do not add any more atoms. (a) the amino acid serine: 車 0-H H-C-H H Н—N—с—с—о—н H (b) нон H-N-C-N-H (c) pyruvic acid: ноо н—с—с—с—о—н H. (d) uracil: H (e) carbonic acid: H-0-C-0-Harrow_forwardPredict which of these compounds are ionic and which are covalent. State your reasoning.(a) BaS(b) CaCO3(c) C6H5Clarrow_forward
- Calculate the Enthalpy Change (ΔH) from average bond energies, which have been listed below in KJ/mol, for the following reaction and identify the nature of the reaction: CH3COOH + CH3OH → CH3COOCH3 + H2O [C‒H: 413; C‒C: 347; C=O: 745; C=C: 614; Cl‒Cl: 239, C‒O: 358; O‒H: 467]arrow_forwardShow the delocalization of charges in the following structures. Draw the resonance forms and indicate the movement of electrons with curved arrows.Hint: First draw the Lewis structure for each the compound.(i) CH2=CH─O-(ii) CH2=CH─O+arrow_forwardThe two compounds nitrogen dioxide and dinitrogen tetraoxide are introduced in Section 3.13. (a) NO2 is an odd-electron compound. Draw the best Lewis diagrams possible for it, recognizing that one atom cannot achieve an octet configuration. Use formal charges to decide whether that should be the (central) nitrogen atom or one of the oxygen atoms. (b) Draw resonance forms for N2O4 that obey the octet rule. The two N atoms are bonded in this molecule.arrow_forward
- Rubbing alcohol is the common name for 2-propanol (iso- propanol), C3H7OH. (a) Draw the three-dimensional structure of the 2-propanol molecule and predict the geometry around each carbon atom. (b) Is the 2-propanol molecule polar or nonpolar? (c) What kinds of intermolecular attractive forces exist between the 2-propanol molecules? (d) The isomer 1-propanol has the same molecular weight as 2-propanol, yet 2-propanol boils at 82.6 °C and 1-propanol boils at 97.2 °C. Explain the difference.arrow_forwardChange ethane into 1,2-ethanediol (HOCH2CH2OH) by removing one hydrogen atom from each carbon atom and replacing with a hydroxide (-OH) group. Draw a Lewis structure for 1,2-ethanediol.arrow_forwardDraw Lewis structures for the following compounds. a) CH2Oarrow_forward
- Formaldehyde, CH2O, is used as an embalming agent. Draw the structure of CH2O, including lone pairs.arrow_forwardConsider the theoretical molecule KrCl3‾. (a) Draw a valid Lewis structure for KrCl3‾. Show all lone pairs and use lines for bonds. Label all non-zeroformal charges on individual atoms and show the overall charge, if it exists, using square brackets.(b) What would you expect to be the molecular geometry for this ion? Fully explain your thought process,including all details about how successive lone pairs should be positioned within this electron geometry.(c) Draw this ion in 3-D, using hashed and wedged bonds as appropriate. Do not worry about labeling the overall or formal charge.arrow_forwardWhich of the following are not related as resonance structures? OH (A) `NH. NH (B) ОН (C) CH2 (D)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
Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning