Chemistry: Structure and Properties & Modified MasteringChemistry with Pearson eText -- ValuePack Access Card -- for Chemistry: Structure and Properties Package
1st Edition
ISBN: 9780133884517
Author: Nivaldo J. Tro
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 7, Problem 44E
Write a hybridization and bonding scheme for each molecule that contains more than one interior atom. Indicate the hybridization about each interior atom. Sketch the structure, including overlapping orbitals, and label all bonds using the notation shown in Examples 6.1 and 6.2.
- C2H2 (skeletal structure HCCH)
- C2H4 (skeletal structure H2CCH2)
- C2H6 (skeletal structure H3CCH3)
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Write a hybridization and bonding scheme for each molecule.Sketch the molecule, including overlapping orbitals, and label allbonds using the notation shown in Examples 6.1 and 6.2.a. CH2Br2b. SO2c. NF3d. BF3
1- Use the molecular orbital model to predict the bond order and magnetism of each of the following molecules.a- COb- CO+c- CO2+
2- Compare and contrast bonding molecular orbitals with antibonding molecularorbitals.
3- Consider the following electron configuration:(σ3s)2(σ3s*)2(σ3p)2(π3p)4(π3p*)4Give four species that, in theory, would have this electron configuration.
4- Predict which substance in each of the following pairs would have the greaterintermolecular forces.I. CO2 or OCSII. SeO2 or SO2III. CH3CH2CH2NH2 or H2NCH2CH2NH2IV. CH3CH3 or H2COV. CH3OH or H2CO
5- Explain why water forms into beads on a waxed car finish.
6- At which temperature does water have its greatest density?
7- At room temperature, F2 and Cl2 are gases, Br2 is a liquid, and I2 is solid. This is because of what?
1.
a) Draw the dominant Lewis structure for the allene molecule (1,2-propyl diene, CH2CCH2 ) and use VSEPR theory to determine the molecule's geometry. In specifying the geometry give all bond angles and specify which nuclei lie in the same plane.
b) Propose a hybridization and bonding scheme for the atoms in allene. That is, specify how each of the atoms is hybridized, which atomic orbitals overlap to form bonding molecular orbitals, and the nature (i.e., 0", 7f, etc.) of these molecular orbitals.
c) Draw a plausible valence molecular orbital level diagram for allene (include only bonding MOs) based on the results from (b).
d) Based on the work from (c) deduce the valence electronic configuration of the ground state of allene.
e) Is the molecule planar or nonplanar? Explain your answer
Chapter 7 Solutions
Chemistry: Structure and Properties & Modified MasteringChemistry with Pearson eText -- ValuePack Access Card -- for Chemistry: Structure and Properties Package
Ch. 7 - Determine the hybridization about 0 in CH3OH.Ch. 7 - Determine the hybridization about C in H2CO.Ch. 7 - According to the valance bond theory, which kind...Ch. 7 - Use molecular orbital theory to determine the bond...Ch. 7 - Use molecular orbital theory to predict which...Ch. 7 - Use molecular orbital theory to determine which...Ch. 7 - Which hybridization scheme occurs about nitrogen...Ch. 7 - Prob. 8SAQCh. 7 - Prob. 9SAQCh. 7 - Prob. 10SAQ
Ch. 7 - Which type of orbitals overlap to form the sigma...Ch. 7 - Prob. 12SAQCh. 7 - Prob. 1ECh. 7 - What is a chemical bond according to valence bond...Ch. 7 - In valence bond theory, what determines the...Ch. 7 - In valence bond theory, the interaction energy...Ch. 7 - What is hybridization? Why is hybridization...Ch. 7 - How does hybridization of the atomic orbitals in...Ch. 7 - How is the number of hybrid orbitals related to...Ch. 7 - Sketch each hybrid orbital sp sp2 sp3 sp3d sp3d2Ch. 7 - Prob. 9ECh. 7 - Name the hybridization scheme that corresponds to...Ch. 7 - What is a chemical bond according to molecular...Ch. 7 - Explain the difference between hybrid atomic...Ch. 7 - What is a bonding molecular orbital?Ch. 7 - Prob. 14ECh. 7 - What is the role of wave interference in...Ch. 7 - Prob. 16ECh. 7 - Prob. 17ECh. 7 - Prob. 18ECh. 7 - Prob. 19ECh. 7 - Prob. 20ECh. 7 - Prob. 21ECh. 7 - When applying molecular orbital theory to...Ch. 7 - In molecular orbital theory, what is a nonbonding...Ch. 7 - Write a short paragraph describing chemical...Ch. 7 - Prob. 25ECh. 7 - Prob. 26ECh. 7 - Prob. 27ECh. 7 - Prob. 28ECh. 7 - Prob. 29ECh. 7 - Prob. 30ECh. 7 - The valence electron configurations of several...Ch. 7 - The valence electron configurations of several...Ch. 7 - Draw orbital diagrams (boxes with arrows in them)...Ch. 7 - Draw orbital diagrams (boxes with arrows in them)...Ch. 7 - Prob. 35ECh. 7 - Draw orbital diagrams (boxes with arrows in them)...Ch. 7 - Which hybridization scheme allows the formation of...Ch. 7 - Which hybridization scheme allows the central atom...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Consider the structure of the amino acid alanine...Ch. 7 - Consider the structure of the amino acid aspartic...Ch. 7 - Sketch the bonding molecular orbital that results...Ch. 7 - Sketch the antibonding molecular orbital that...Ch. 7 - Draw an MO energy diagram and predict the bond...Ch. 7 - Draw an MO energy diagram and predict the bond...Ch. 7 - Sketch the bonding and antibonding molecular...Ch. 7 - Sketch the bonding and antibonding molecular...Ch. 7 - Using the molecular orbital energy ordenng for...Ch. 7 - Using the molecular orbital energy ordering for...Ch. 7 - Apply molecular orbital theory to predict if each...Ch. 7 - Apply molecular orbital theory to predict if each...Ch. 7 - According to MO theory, which molecule or ion has...Ch. 7 - According to MO theory, which molecule or ion has...Ch. 7 - Draw an MO energy diagram for CO. (Use the energy...Ch. 7 - Draw an MO energy diagram for HCI. Predict the...Ch. 7 - Prob. 61ECh. 7 - Prob. 62ECh. 7 - Prob. 63ECh. 7 - Prob. 64ECh. 7 - Prob. 65ECh. 7 - Prob. 66ECh. 7 - For each compound, draw the Lewis structure,...Ch. 7 - For each compound, draw the Lewis structure,...Ch. 7 - Amino acids are biological compounds that link...Ch. 7 - The genetic code is based on four different bases...Ch. 7 - The structure of caffeine, present in coffee and...Ch. 7 - The structure of acetylsalicylic acid (aspirin) is...Ch. 7 - Draw a molecular orbital energy diagram for CIF....Ch. 7 - Draw Lewis structures and MO diagrams for CN+, CN,...Ch. 7 - Bromine can form compounds or ions with any number...Ch. 7 - The compound C3H4 has two double bonds. Describe...Ch. 7 - How many hybrid orbitals do we use to describe...Ch. 7 - Prob. 78ECh. 7 - In VSEPR theory, which uses the Lewis model to...Ch. 7 - The resuts of a molecular orbital calculation for...Ch. 7 - Prob. 81ECh. 7 - cis-2-Butene isomerizes (changes its structure) to...Ch. 7 - The ion CH5 + can form under very special...Ch. 7 - Neither the VSEPR model nor the hybridization...Ch. 7 - Prob. 85ECh. 7 - The most stable forms of the nonmetals in groups...Ch. 7 - Consider the bond energies of three iodine...Ch. 7 - How many atomic orbitals form a set of sp3hybrid...
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
- Allene (1,2-propadicne), a gas, has the following structure: What is the hybridization at each carbon atom? What is the geometry about each carbon atom? Using valencebond theory, describe the bonding about the center carbon atom. 1,3-dichloroallene is a derivative of allene with the following structure: Is this a polar molecule? (If you have difficulty visualizing the structure of this molecule, you might build a molecular model of it.)arrow_forwardMethylcyanoacrylate is the active ingredient in super glues. Its Lewis structure is (a) How many sigma bonds are in the molecule? (b) How many pi bonds are in the molecule? (c) What is the hybridization of the carbon atom bonded to nitrogen? (d) What is the hybridization of the carbon atom bonded to oxygen? (e) What is the hybridization of the double-bonded oxygen?arrow_forwardThere are two compounds with the molecular formula HN3. One is called hydrogen azide; the other is cyclotriazene. (a) Write the Lewis structure for each compound. (b) Designate the hybridization of each nitrogen in hydrogen azide. (c) What is the hybridization of each nitrogen in cyclotriazene? (d) How many sigma bonds are in hydrogen azide? In cyclotriazene? (e) How many pi bonds are in hydrogen azide? In cyclotriazene? (f) Give approximate values for the N-to-N-to-N bond angles in each molecule.arrow_forward
- 7.59 What type of hybrid orbital is generated by combining the valence s orbital and all three valence p orbitals of an atom? How many hybrid orbitals result?arrow_forwardGive the hybridization of each central atom in the following molecules. (a) cyclohexene (b) phosgene, Cl2CO (c) glycine, H2NC(1)H2C(2)OOH (Note: Numbers in parentheses label each carbon atom.)arrow_forwardIn the molecular orbital mode l, compare and contrast bonds with bonds. What orbitals form the bonds and what orbitals form the bonds? Assume the z-axis is the internuclear axis.arrow_forward
- Aspartame is a compound that is 200 times sweeter than sugar and is used extensively (under the trade name NutraSweet) in diet soft drinks. The skeleton structure of the atoms in aspartame is (a) Complete the Lewis structure and give the number of and bonds in aspartame. (b) What is the hybridization about each carbon atom that forms a double bond with an oxygen atom? (c) What is the hybridization about each nitrogen atom?arrow_forwardThe bond length in C2 is 131 pm. Compare this with the bond lengths in C2H2 (120 pm), C2H4 (134 pm), and C2H6 (153 pm). What bond order would you predict for C2 from its bond length? Does this agree with the molecular orbital configuration you would predict for C2?arrow_forwardSpecify the electron-pair and molecular geometry for each underlined atom in the following list. Describe the hybrid orbital set used by this atom in each molecule or ion. (a) CSe2 (b) SO2 (c) CH2O (d) NH4ssarrow_forward
- Strike-anywhere matches contain a layer of KClO3 and a layer of P4S3. The heat produced by the friction of striking the match causes these two compounds to react vigorously, which sets fire to the wooden stem of the match. KCIO3 contains the ClO3 ion. P4S3 is an unusual molecule with the skeletal structure. (a) Write Lewis structures for P4S3 and the ClO3 ion. (b) Describe the geometry about the P atoms, the S atom, and the Cl atom in these species. (c) Assign a hybridization to the P atoms, the S atom, and the Cl atom in these species. (d) Determine the oxidation states and formal charge of the atoms in P4S3 and the ClO3 ion.arrow_forwardMinoxidil (C9H15N15O) is a compound produced by the Pharmacia Upjohn Company that has been approved as a treatment for some types of male pattern baldness. Note that in such shorthand ring structures, each point where lines meet is a carbon atom and that the hydrogen atoms bonded to the carbon atoms in the rings have been omitted. There will be four bonds to each carbon atom. a. Give the hybridization of the five nitrogen atoms in minoxidil. b. Give the hybridization of each of the nine carbon atoms in minoxidil. c. Give the approximate values for the bond angles marked a, b, c, d, e, and f. d. Including all the hydrogen atoms, how many bonds exist in minoxidil? e. How many bonds exist in minoxidil?arrow_forwardThe structure of amphetamine, a stimulant, is shown below. (Replacing one H atom on the NH2, or amino, group with CH3 gives methamphetamine a particularly dangerous drug commonly known as speed.) (a) What are the hybrid orbitals used by the C atoms of the C6 ring. by the C atoms of the side chain, and by the N atom? (b) Give approximate values for the bond angles A, B, and C. (c) How many bonds and bonds are in the molerule? (d) Is the molecule polar or nonpolar? (e) Amphetamine reacts readily with a proton (H+) in aqueous solution. Where does this proton attach to the molecule? Explain how the electrostatic potential map predicts this site of protonation.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry for Engineering StudentsChemistryISBN:9781285199023Author:Lawrence S. Brown, Tom HolmePublisher:Cengage Learning
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStax
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:9781285199023
Author:Lawrence S. Brown, Tom Holme
Publisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
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
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