Chemistry: An Atoms First Approach
2nd Edition
ISBN: 9781305079243
Author: Steven S. Zumdahl, Susan A. Zumdahl
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 4, Problem 91AE
Interpretation Introduction
Interpretation: The prediction made for molecular structures obtained in Exercise 99 being same as the one made in Exercise 100 is to be validated.
Concept introduction: Lewis structures represent the rearrangement of valence electrons in a molecule. It represents covalent bonding in a molecule or ion.
To determine: If the prediction for molecular structures in Exercise 99 is same as for the one in Exercise 100 or not.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Show the curved arrow mechanism and both products for the reaction between methyl iodide and propoxide.
1st attempt
NV
H
10:
H
H
1
Add the missing curved arrow notation.
H
+
See Periodic Table
First I wanted to see if you would mind checking my graphs behind me. (They haven't been coming out right)? Second, could you help me explain if the rate of reaction is proportional to iodide and persulfate of each graph. I highlighted my answer and understanding but I'm not sure if I'm on the right track. Thank you in advance.
The heat of combustion for ethane, C2H6C2H6 , is 47.8 kJ/g. How much heat is produced if 1.65 moles of ethane undergo complete combustion?
Chapter 4 Solutions
Chemistry: An Atoms First Approach
Ch. 4 - Explain the main postulate of the VSEPR model....Ch. 4 - Explain why CF4 and Xef4 are nonpolar compounds...Ch. 4 - Consider the following compounds: CO2, SO2, KrF2,...Ch. 4 - Prob. 4RQCh. 4 - What hybridization is required for central atoms...Ch. 4 - Prob. 6RQCh. 4 - Prob. 7RQCh. 4 - What are molecular orbitals? How do they compare...Ch. 4 - Explain the difference between the and MOs for...Ch. 4 - Prob. 3ALQ
Ch. 4 - Which of the following would you expect to be more...Ch. 4 - Arrange the following molecules from most to least...Ch. 4 - Which is the more correct statement: The methane...Ch. 4 - Prob. 7ALQCh. 4 - Prob. 8ALQCh. 4 - Which of the following statements is/are true?...Ch. 4 - Give one example of a compound having a linear...Ch. 4 - In the hybrid orbital model, compare and contrast ...Ch. 4 - Prob. 13QCh. 4 - Prob. 14QCh. 4 - Prob. 15QCh. 4 - Prob. 16QCh. 4 - Compare and contrast bonding molecular orbitals...Ch. 4 - Prob. 18QCh. 4 - Why does the molecular orbital model do a better...Ch. 4 - The three NO bonds in NO3 are all equivalent in...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - Predict the molecular structure and bond angles...Ch. 4 - Prob. 24ECh. 4 - Prob. 25ECh. 4 - Two variations of the octahedral geometry (see...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - State whether or not each of the following has a...Ch. 4 - The following electrostatic potential diagrams...Ch. 4 - Which of the molecules in Exercises 21 and 22 have...Ch. 4 - Which of the molecules in Exercises 27 and 28 have...Ch. 4 - Write Lewis structures and predict the molecular...Ch. 4 - Write Lewis structures and predict whether each of...Ch. 4 - Consider the following Lewis structure where E is...Ch. 4 - Consider the following Lewis structure where E is...Ch. 4 - The molecules BF3, CF4, CO2, PF5, and SF6 are all...Ch. 4 - Two different compounds have the formula XeF2Cl2....Ch. 4 - Use the localized electron model to describe the...Ch. 4 - Use the localized electron model to describe the...Ch. 4 - Use the localized electron model to describe the...Ch. 4 - Use the localized electron model to describe the...Ch. 4 - The space-filling models of ethane and ethanol are...Ch. 4 - The space-filling models of hydrogen cyanide and...Ch. 4 - Prob. 45ECh. 4 - Prob. 46ECh. 4 - Prob. 47ECh. 4 - Give the expected hybridization of the central...Ch. 4 - For each of the following molecules, write the...Ch. 4 - For each of the following molecules or ions that...Ch. 4 - Prob. 51ECh. 4 - The allene molecule has the following Lewis...Ch. 4 - Indigo is the dye used in coloring blue jeans. The...Ch. 4 - Prob. 54ECh. 4 - Prob. 55ECh. 4 - Many important compounds in the chemical industry...Ch. 4 - Two molecules used in the polymer industry are...Ch. 4 - Hot and spicy foods contain molecules that...Ch. 4 - One of the first drugs to be approved for use in...Ch. 4 - The antibiotic thiarubin-A was discovered by...Ch. 4 - Prob. 61ECh. 4 - Sketch the molecular orbital and label its type (...Ch. 4 - Prob. 63ECh. 4 - Which of the following are predicted by the...Ch. 4 - Prob. 65ECh. 4 - Prob. 66ECh. 4 - Prob. 67ECh. 4 - Using the molecular orbital model to describe the...Ch. 4 - Prob. 69ECh. 4 - A Lewis structure obeying the octet rule can be...Ch. 4 - Using the molecular orbital model, write electron...Ch. 4 - Using the molecular orbital model, write electron...Ch. 4 - In which of the following diatomic molecules would...Ch. 4 - In terms of the molecular orbital model, which...Ch. 4 - Prob. 75ECh. 4 - Show how a hydrogen 1s atomic orbital and a...Ch. 4 - Use Figs. 4-54 and 4-55 to answer the following...Ch. 4 - The diatomic molecule OH exists in the gas phase....Ch. 4 - Prob. 79ECh. 4 - Describe the bonding in NO+, NO, and NO, using...Ch. 4 - Describe the bonding in the O3 molecule and the...Ch. 4 - Prob. 82ECh. 4 - Prob. 83AECh. 4 - Vitamin B6 is an organic compound whose deficiency...Ch. 4 - Two structures can be drawn for cyanuric acid: a....Ch. 4 - Prob. 86AECh. 4 - What do each of the following sets of...Ch. 4 - Aspartame is an artificial sweetener marketed...Ch. 4 - Prob. 89AECh. 4 - The three most stable oxides of carbon are carbon...Ch. 4 - Prob. 91AECh. 4 - Which of the following molecules have net dipole...Ch. 4 - The strucrure of TeF5 is Draw a complete Lewis...Ch. 4 - Complete the following resonance structures for...Ch. 4 - Prob. 95AECh. 4 - Describe the bonding in the first excited state of...Ch. 4 - Using an MO energy-level diagram, would you expect...Ch. 4 - Show how a dxz. atomic orbital and a pz, atomic...Ch. 4 - What type of molecular orbital would result from...Ch. 4 - Consider three molecules: A, B, and C. Molecule A...Ch. 4 - Prob. 101CWPCh. 4 - Predict the molecular structure, bond angles, and...Ch. 4 - Draw the Lewis structures for SO2, PCl3, NNO, COS,...Ch. 4 - Draw the Lewis structures for TeCl4, ICl5, PCl5,...Ch. 4 - A variety of chlorine oxide fluorides and related...Ch. 4 - Pelargondin is the molecule responsible for the...Ch. 4 - Complete a Lewis structure for the compound shown...Ch. 4 - Prob. 108CWPCh. 4 - Consider the molecular orbital electron...Ch. 4 - Place the species B2+ , B2, and B2 in order of...Ch. 4 - The compound NF3 is quite stable, but NCl3 is very...Ch. 4 - Predict the molecular structure for each of the...Ch. 4 - Prob. 113CPCh. 4 - Cholesterol (C27liu;O) has the following...Ch. 4 - Cyanamide (H2NCN), an important industrial...Ch. 4 - As compared with CO and O2, CS and S2 are very...Ch. 4 - Prob. 117CPCh. 4 - Use the MO model to explain the bonding in BeH2....Ch. 4 - Prob. 119CPCh. 4 - Arrange the following from lowest to highest...Ch. 4 - Prob. 121CPCh. 4 - Prob. 122CPCh. 4 - Carbon monoxide (CO) forms bonds to a variety of...Ch. 4 - The space-filling model for benzoic acid, a food...Ch. 4 - As the bead engineer of your starship in charge of...Ch. 4 - A flask containing gaseous N2 is irradiated with...Ch. 4 - Determine the molecular structure and...
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
- Review of this week's reaction: H2NCN (cyanamide) + CH3NHCH2COOH (sarcosine) + NaCl, NH4OH, H2O ----> H2NC(=NH)N(CH3)CH2COOH (creatine) Q7. Draw by hand the reaction of creatine synthesis listed above using line structures without showing the Cs and some of the Hs, but include the lone pairs of electrons wherever they apply. (4 pts) Q8. Considering the Zwitterion form of an amino acid, draw the Zwitterion form of Creatine. (2 pts) Q9. Explain with drawing why the C—N bond shown in creatine structure below can or cannot rotate. (3 pts)arrow_forwardWould the following organic synthesis occur in one step? Add any missing products, required catalysts, inorganic reagents, and other important conditions. Please include a detailed explanation and drawings showing how the reaction may occur in one step.arrow_forwardPlease help me answer a. Please and thank you I advance.arrow_forward
- Draw both of the chair flips for both the cis and trans isomers for the following compounds: 1,4-diethylcyclohexane 1-methyl-3-secbutylcyclohexanearrow_forwardPpplllleeeaaasssseeee hellppp wiithhh thisss physical chemistryyyyy I talked like this because AI is very annoyingarrow_forwardFor this question, if the product is racemic, input both enantiomers in the same Marvin editor. A) Input the number that corresponds to the reagent which when added to (E)-but-2-ene will result in a racemic product. Input 1 for Cl, in the cold and dark Input 2 for Oy followed by H₂O, Zn Input 3 for D₂ with metal catalyst Input 4 for H₂ with metal catalyst B) Draw the skeletal structure of the major organic product made from the reagent in part A Marvin JS Help Edit drawing C) Draw the skeletal structure of the major organic product formed when (2)-but-2-ene is treated with peroxyacetic acid. Marvin 35 Helparrow_forward
- Michael Reactions 19.52 Draw the products from the following Michael addition reactions. 1. H&C CH (a) i 2. H₂O* (b) OEt (c) EtO H₂NEt (d) ΕΙΟ + 1. NaOEt 2. H₂O' H H 1. NaOEt 2. H₂O*arrow_forwardRank the labeled protons (Ha-Hd) in order of increasing acidity, starting with the least acidic. НОН НЬ OHd Онсarrow_forwardCan the target compound at right be efficiently synthesized in good yield from the unsubstituted benzene at left? ? starting material target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. + More... Note for advanced students: you may assume that you are using a large excess of benzene as your starting material. C :0 T Add/Remove step Garrow_forward
- The following equations represent the formation of compound MX. What is the AH for the electron affinity of X (g)? X₂ (g) → 2X (g) M (s) → M (g) M (g) M (g) + e- AH = 60 kJ/mol AH = 22 kJ/mol X (g) + e-X (g) M* (g) +X (g) → MX (s) AH = 118 kJ/mol AH = ? AH = -190 kJ/mol AH = -100 kJ/mol a) -80 kJ b) -30 kJ c) -20 kJ d) 20 kJ e) 156 kJarrow_forwardA covalent bond is the result of the a) b) c) d) e) overlap of two half-filled s orbitals overlap of a half-filled s orbital and a half-filled p orbital overlap of two half-filled p orbitals along their axes parallel overlap of two half-filled parallel p orbitals all of the abovearrow_forwardCan the target compound at right be efficiently synthesized in good yield from the unsubstituted benzene at left? starting material target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. + More... Note for advanced students: you may assume that you are using a large excess of benzene as your starting material. C T Add/Remove step X ноarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
Chemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStax
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Principles of Modern ChemistryChemistryISBN:9781305079113Author:David W. Oxtoby, H. Pat Gillis, Laurie J. ButlerPublisher:Cengage Learning
Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:9781938168390
Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:OpenStax
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Principles of Modern Chemistry
Chemistry
ISBN:9781305079113
Author:David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
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 for Engineering Students
Chemistry
ISBN:9781337398909
Author:Lawrence S. Brown, Tom Holme
Publisher: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