Chemistry: The Central Science, Books a la Carte Edition & Solutions to Red Exercises for Chemistry & Mastering Chemistry with Pearson eText -- Access Card Package
1st Edition
ISBN: 9780134024516
Author: Theodore E. Brown, H. Eugene LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward, Matthew E. Stoltzfus
Publisher: PEARSON
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Chapter 9, Problem 74E
(a) What is the probability of finding an electron on the internuclear axis if the electron occupies a iT molecular orbital?
(b) For a hornonuclear diatomic molecule, what similarities and differences are there between the lT2p MO made from the 2pxatomic orbitals and the
(c) How do the
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The molecular orbitals depicted below are derived from 2p atomic orbitals in F₂⁺. (a) Give the orbital designations. (b) Which is occupied by at least one electron in F₂⁺? (c) Which is occupied by only one electron in F₂⁺?
If an electron is removed from a fluorine molecule, an F+2molecular ion forms.(a) Give the molecular electron configurations for F2 and F+2 (for the MOs constructed from valence AOs).(b) Give the bond order of each species.(c) Predict which species should be paramagnetic.(d) Predict which species has the greater bond dissociation energy.
The iodine bromide molecule, IBr, is an interhalogen compound.Assume that the molecular orbitals of IBr are analogous tothe homonuclear diatomic molecule F2. (a) Which valenceatomic orbitals of I and of Br are used to construct the MOs ofIBr? (b) What is the bond order of the IBr molecule? (c) One ofthe valence MOs of IBr is sketched here. Why are the atomicorbital contributions to this MO different in size? (d) What isthe label for the MO sketched below? (e) For the IBr molecule,how many electrons occupy the MO sketched below?
Chapter 9 Solutions
Chemistry: The Central Science, Books a la Carte Edition & Solutions to Red Exercises for Chemistry & Mastering Chemistry with Pearson eText -- Access Card Package
Ch. 9.2 - Prob. 9.1.1PECh. 9.2 - Prob. 9.1.2PECh. 9.2 - Prob. 9.2.1PECh. 9.2 - Prob. 9.2.2PECh. 9.2 - Prob. 9.3.1PECh. 9.2 - Prob. 9.3.2PECh. 9.3 - Prob. 9.4.1PECh. 9.3 - Prob. 9.4.2PECh. 9.5 - Prob. 9.5.1PECh. 9.5 - Prob. 9.5.2PE
Ch. 9.6 - Prob. 9.6.1PECh. 9.6 - Prob. 9.6.2PECh. 9.6 - Prob. 9.7.1PECh. 9.6 - Prob. 9.7.2PECh. 9.7 - Prob. 9.8.1PECh. 9.7 - Prob. 9.8.2PECh. 9.8 - Prob. 9.9.1PECh. 9.8 - Prob. 9.9.2PECh. 9 - Prob. 1DECh. 9 - Prob. 1ECh. 9 - Prob. 2ECh. 9 - Prob. 3ECh. 9 - Prob. 4ECh. 9 - Prob. 5ECh. 9 - Prob. 6ECh. 9 - Prob. 7ECh. 9 - Prob. 8ECh. 9 - Prob. 9ECh. 9 - Prob. 10ECh. 9 - Prob. 11ECh. 9 - Prob. 12ECh. 9 - Prob. 13ECh. 9 - Prob. 14ECh. 9 - Prob. 15ECh. 9 - Prob. 16ECh. 9 - Prob. 17ECh. 9 - Prob. 18ECh. 9 - Prob. 19ECh. 9 - Prob. 20ECh. 9 - Prob. 21ECh. 9 - Prob. 22ECh. 9 - Prob. 23ECh. 9 - Prob. 24ECh. 9 - Prob. 25ECh. 9 - Prob. 26ECh. 9 - Prob. 27ECh. 9 - Prob. 28ECh. 9 - Prob. 29ECh. 9 - Prob. 30ECh. 9 - Prob. 31ECh. 9 - Prob. 32ECh. 9 - Prob. 33ECh. 9 - Prob. 34ECh. 9 - Prob. 35ECh. 9 - Prob. 36ECh. 9 - Prob. 37ECh. 9 - Prob. 38ECh. 9 - Prob. 39ECh. 9 - Prob. 40ECh. 9 - Prob. 41ECh. 9 - Prob. 42ECh. 9 - Prob. 43ECh. 9 - Describe the intermediate that is thought to form...Ch. 9 - Prob. 45ECh. 9 - Prob. 46ECh. 9 - Prob. 47ECh. 9 - Prob. 48ECh. 9 - (a) Starting with the orbital diagram of a boron...Ch. 9 - Prob. 50ECh. 9 - Prob. 51ECh. 9 - Prob. 52ECh. 9 - Prob. 53ECh. 9 - Prob. 54ECh. 9 - Prob. 55ECh. 9 - Prob. 56ECh. 9 - Prob. 57ECh. 9 - Prob. 58ECh. 9 - Prob. 59ECh. 9 - Prob. 60ECh. 9 - Prob. 61ECh. 9 - Prob. 62ECh. 9 - Prob. 63ECh. 9 - Prob. 64ECh. 9 - In the formate ion, HCO2-, the carbon atom is the...Ch. 9 -
9.66 Consider the Lewis structure shown below....Ch. 9 - Prob. 67ECh. 9 - Prob. 68ECh. 9 - Prob. 69ECh. 9 - Prob. 70ECh. 9 - Prob. 71ECh. 9 - Prob. 72ECh. 9 - Prob. 73ECh. 9 - (a) What is the probability of finding an electron...Ch. 9 - Prob. 75ECh. 9 - Prob. 76ECh. 9 - Prob. 77ECh. 9 - Prob. 78ECh. 9 - Prob. 79ECh. 9 - Prob. 80ECh. 9 - Prob. 81ECh. 9 - Prob. 82ECh. 9 - Prob. 83ECh. 9 - Prob. 84ECh. 9 - Prob. 85AECh. 9 - Prob. 86AECh. 9 - Prob. 87AECh. 9 - Prob. 88AECh. 9 - Prob. 89AECh. 9 - Prob. 90AECh. 9 - Prob. 91AECh. 9 - Prob. 92AECh. 9 - Prob. 93AECh. 9 - Prob. 94AECh. 9 - Prob. 95AECh. 9 - Prob. 96AECh. 9 - Prob. 97AECh. 9 - Prob. 98AECh. 9 - A typical amino acid with one amino group and one...Ch. 9 - The azide ion, N3-, is linear with two N—N bonds...Ch. 9 - Prob. 101AECh. 9 - Prob. 102AECh. 9 - Prob. 103AECh. 9 - Prob. 104AECh. 9 - Prob. 105AECh. 9 - Prob. 106AECh. 9 - How many hydrogen atoms are in 2, 2-...Ch. 9 - Prob. 108AECh. 9 - Prob. 109AECh. 9 - Prob. 110AECh. 9 - Prob. 111AECh. 9 - Prob. 112AECh. 9 - Prob. 113IECh. 9 - Prob. 114IECh. 9 - Prob. 115IECh. 9 - Prob. 116IECh. 9 - Practice Exercise 2 Name the dipeptide and give...Ch. 9 - How many chiral carbon atoms are there in the...Ch. 9 - Prob. 119IECh. 9 - Prob. 120IECh. 9 - Prob. 121IECh. 9 - Prob. 122IE
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- The compound sketched below is acetylsalicylic acid, commonly known as aspirin. (a) What are the approximate values of the angles marked A, B, C, and D? (b) What hybrid orbitals are used by carbon atoms 1, 2, and 3ss?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_forwardIn each of the following molecules, a central atom is surrounded by a total of three atoms or unshared electron pairs: SnCl2, BCl3, SO2. In which of these molecules would you expect the bond angle to be less than 120? Explain your reasoning.arrow_forward
- Aspirin, or acetylsalicylic acid, has the formula C9H8O4 and the skeleton structure (a) Complete the Lewis structure and give the number of bonds and bonds in aspirin. (b) What is the hybridization about the CO2H carbon atom (colored blue)? (c) What is the hybridization about the carbon atom in the benzene-like ring that is bonded to an oxygen atom (colored red)? Also, what is the hybridization of the oxygen atom bonded to this carbon atom?arrow_forwardCompare and contrast the molecular orbital and ionic bonding descriptions of LiF.arrow_forwardDo lone pairs about a central atom affect the hybridization of the central atom? If so, how?arrow_forward
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- The diagram that follows shows the highest-energy occupiedMOs of a neutral molecule CX, where element X is in thesame row of the periodic table as C. (a) Based on the numberof electrons, can you determine the identity of X? (b) Wouldthe molecule be diamagnetic or paramagnetic? (c) Considerthe π2p MOs of the molecule. Would you expect them to havea greater atomic orbital contribution from C, have a greateratomic orbital contribution from X, or be an equal mixtureof atomic orbitals from the two atoms?arrow_forwardWhy does the energy ordering of the molecular orbitals of the second-period diatomic molecules change in going from N2 to O2?arrow_forwardEthyl acetate, C4H8O2, is a fragrant substance used both as asolvent and as an aroma enhancer. Its Lewis structure is (a) What is the hybridization at each of the carbon atomsof the molecule? (b) What is the total number of valenceelectrons in ethyl acetate? (c) How many of the valence electronsare used to make s bonds in the molecule? (d) Howmany valence electrons are used to make p bonds? (e) Howmany valence electrons remain in nonbonding pairs in themolecule?arrow_forward
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