General Chemistry: Atoms First
2nd Edition
ISBN: 9780321809261
Author: John E. McMurry, Robert C. Fay
Publisher: Prentice Hall
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 5.3, Problem 5.5P
Describe the bonding in propane, C3H8, a fuel often used in rural homes and campers, and tell what kinds of orbitals on each atom overlap to form the C─C and C─H bonds.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
How would you describe the molecular geometry of C2H2F2, and what are its bond angles?
Draw the molecular shapes and predict the bond angles (relative to the ideal angles) of (a) PF3 and (b) COCl2.
For the carbonate ion, CO3 2−, draw all of the resonance structures. Identify which orbitals overlap to create each bond.
Chapter 5 Solutions
General Chemistry: Atoms First
Ch. 5.1 - Predict the shapes of the following molecules or...Ch. 5.1 - Acetic acid, CH3CO2H, is the main organic...Ch. 5.1 - Benzene, C6H6, is a cyclic molecule in which all...Ch. 5.1 - What is the geometrical arrangement of charge...Ch. 5.3 - Describe the bonding in propane, C3H8, a fuel...Ch. 5.4 - Describe the hybridization of the carbon atom in...Ch. 5.4 - Describe the hybridization of each carbon atom in...Ch. 5.4 - Describe the hybridization of the carbon atom in...Ch. 5.4 - Describe the hybridization of the carbon atom in...Ch. 5.4 - Describe the hybridization of the carbon atom in...
Ch. 5.4 - Identify each of the following sets of hybrid...Ch. 5.4 - The following ball-and-stick molecular model is a...Ch. 5.5 - Construct an MO diagram for the He2+ ion. Is this...Ch. 5.6 - The B2 and C2 molecules have MO diagrams similar...Ch. 5.7 - Draw two electron-dot resonance structures for the...Ch. 5.7 - Why is molecular shape so important in biological...Ch. 5.7 - Prob. 5.17CPCh. 5 - What is the geometry around the central atom in...Ch. 5 - Prob. 5.19CPCh. 5 - Prob. 5.20CPCh. 5 - Prob. 5.21CPCh. 5 - Prob. 5.22CPCh. 5 - Prob. 5.23CPCh. 5 - Prob. 5.24SPCh. 5 - Prob. 5.25SPCh. 5 - Prob. 5.26SPCh. 5 - How many charge clouds are there around central...Ch. 5 - Prob. 5.28SPCh. 5 - Prob. 5.29SPCh. 5 - What shape do you expect for each of the following...Ch. 5 - Prob. 5.31SPCh. 5 - Prob. 5.32SPCh. 5 - Prob. 5.33SPCh. 5 - What bond angles do you expect for each of the...Ch. 5 - Prob. 5.35SPCh. 5 - Prob. 5.36SPCh. 5 - Prob. 5.37SPCh. 5 - Prob. 5.38SPCh. 5 - A potential replacement for the chlorofluorocarbon...Ch. 5 - Prob. 5.40SPCh. 5 - Prob. 5.41SPCh. 5 - Prob. 5.42SPCh. 5 - Prob. 5.43SPCh. 5 - What hybridization do you expect for atoms that...Ch. 5 - Prob. 5.45SPCh. 5 - Prob. 5.46SPCh. 5 - What hybridization would you expect for the...Ch. 5 - Prob. 5.48SPCh. 5 - Prob. 5.49SPCh. 5 - Prob. 5.50SPCh. 5 - Prob. 5.51SPCh. 5 - Prob. 5.52SPCh. 5 - Prob. 5.53SPCh. 5 - Prob. 5.54SPCh. 5 - Prob. 5.55SPCh. 5 - Prob. 5.56SPCh. 5 - Prob. 5.57SPCh. 5 - Prob. 5.58SPCh. 5 - Prob. 5.59SPCh. 5 - Prob. 5.60SPCh. 5 - Prob. 5.61SPCh. 5 - Prob. 5.62CHPCh. 5 - The following molecular model is a representation...Ch. 5 - Prob. 5.64CHPCh. 5 - Prob. 5.65CHPCh. 5 - Prob. 5.66CHPCh. 5 - Prob. 5.67CHPCh. 5 - Calcium carbide, CaC2, reacts with water to...Ch. 5 - Prob. 5.69CHPCh. 5 - The N2O5 molecule has six NO bonds and two NO ...Ch. 5 - In the cyanate ion, OCN, carbon is the central...Ch. 5 - Aspirin has the following connections among atoms....Ch. 5 - Prob. 5.73CHPCh. 5 - At high temperatures, sulfur vapor is...Ch. 5 - Carbon monoxide is produced by incomplete...Ch. 5 - Prob. 5.76CHPCh. 5 - Prob. 5.77CHPCh. 5 - Prob. 5.78CHPCh. 5 - The diatomic cyanide ion (CN) and nitrosonium ion...Ch. 5 - Prob. 5.80MPCh. 5 - Prob. 5.81MPCh. 5 - Prob. 5.82MP
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
- It is possible to write a simple Lewis structure for the SO42- ion, involving only single bonds, which follows the octet rule. However, Linus Pauling and others have suggested an alternative structure, involving double bonds, in which the sulfur atom is surrounded by six electron pairs. (a) Draw the two Lewis structures. (b) What geometries are predicted for the two structures? (c) What is the hybridization of sulfur in each case? (d) What are the formal charges of the atoms in the two structures?arrow_forwardTwo compounds have the molecular formula N3H3. One of the compounds, triazene, contains an NN bond; the other compound, triaziridene, does not. (a) Write the correct Lewis structures for each compound. (b) Approximate the bond angle between the three nitrogen atoms in each compound.arrow_forwardFormamide, HC(O)NH2, is prepared at high pressures from carbon monoxide and ammonia, and serves as an industrial solvent (the parentheses around the O indicate that it is bonded only to the carbon atom and that the carbon atom is also bonded to the H and the N atoms). Two resonance forms (one with formal charges) can be written for formamide. Write both resonance structures, and predict the bond angles about the carbon and nitrogen atoms for each resonance form. Are they the same? Describe how the experimental determination of the HNH bond angle could be used to indicate which resonance form is more important.arrow_forward
- The sulfamate ion, H2NSO3, can be thought of as having been formed from the amide ion, NH2, and sulphur trioxide, SO3. (a) What are the electron-pair and molecular geometries or the amide ion and or SO3? What are the hybridizations of the N and S atoms, respectively? (b) Sketch a structure for the sulfamate ion, and estimate the bond angles. (c) What changes in hybridization do you expect for N and S in the course of the reaction NH2 + SO3 H2NSO3? (d) Is SO3 the donor of an electron pair or the acceptor of an electron pair in the reaction with amide ion? Does the electrostatic potential map shown below confirm your prediction?arrow_forwardWhat is the shape of the dichloromethane (CH2C12) molecule? Predict the Cl —C —Clbond angle.arrow_forwardDraw the best Lewis dot structure for BrO₄⁻, being sure to give the electronic geometry, molecular geometry, hybridization of the central element, polarity, and bond angle around the central element.arrow_forward
- Describe the bond angles to be found in each of the following molecular structures: (a) trigonal planar, (b) tetrahedral, (c) octahedral, (d) linear.arrow_forwardWrite the best Lewis dot structure for NH₄⁺, being sure to give the electronic geometry, molecular geometry, hybridization of the central element, polarity, and bond angle around the central element.arrow_forwardDraw the Lewis structure of the molecule. What do you predict for the bond order of the C¬S bonds?arrow_forward
- Draw the Lewis structure for chloroform, CHCl3. What are its electron-pair and molecular geometries? What orbitals on C, H, and Cl overlap to form bonds involving these elements?arrow_forward17) What are the "theoretical" values for the C−C≡C bond angles?arrow_forwardWrite the best Lewis dot structure for N₃⁻, give the electronic geometry, molecular geometry, hybridization of the central element, polarity, and bond angle around the central element.arrow_forward
arrow_back_ios
arrow_forward_ios
Recommended textbooks for you
- Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
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: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
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