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 solutionChapter 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
- The 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_forwardThe 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_forwardDescribe the hybridization around the central atom and the bonding in SCl2 and OCS.arrow_forward
- Draw the Lewis structure for 1, 1-dimethylhydrazine [(CH3)2NNH2, a compound used as a rocket fuel]. What: is the hybridization for the two nitrogen atoms in this molecule? What orbitals overlap to form the bond between the nitrogen atoms?arrow_forwarda Nitrogen trifluoride, NF3, is a relatively unreactive, colorless gas. How would you describe the bonding in the NF3 molecule in terms of valence bond theory? Use hybrid orbitals. b Silicon tetrafluoride, SiF4, is a colorless gas formed when hydrofluoric acid attacks silica (SiO2) or glass. Describe the bonding in the SiF4 molecule, using valence bond theory.arrow_forwardA neutral molecule is identified as a tetrafluoride, XF4, where X is an unknown atom. If the molocule has a dipole moment of 0.63 D, can you give some possibilities for the identity of X?arrow_forward
arrow_back_ios
arrow_forward_ios
Recommended textbooks for you
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher: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 & 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: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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