Student Solutions Manual for Oxtoby/Gillis/Butler's Principles of Modern Chemistry, 8th
8th Edition
ISBN: 9798214170251
Author: David W. Oxtoby, H. Pat Gillis and Laurie J. Butler
Publisher: Cengage Learning US
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Chapter 3, Problem 38P
The percent ionic character of the bonds in several interhalogen Molecules (as estimated from their measured dipole moments and bond lengths) are ClF (11%), BrF(15%), BrCl (5.6%), ICl(5.8%), and IBr (10%). Estimate the percent ionic characters for each of these molecules, using the equation in Problem 37, and compare them with the given values.
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Chapter 3 Solutions
Student Solutions Manual for Oxtoby/Gillis/Butler's Principles of Modern Chemistry, 8th
Ch. 3 - Before the element scandium was discovered in...Ch. 3 - Prob. 2PCh. 3 - Prob. 3PCh. 3 - Prob. 4PCh. 3 - Prob. 5PCh. 3 - A gold nucleus is located at the origin of...Ch. 3 - Prob. 7PCh. 3 - A gold nucleus is located at the origin of...Ch. 3 - Prob. 9PCh. 3 - Prob. 10P
Ch. 3 - Use the data in Table 3.1 to plot the logarithm of...Ch. 3 - Use the data in Table 3.1 to plot the logarithm of...Ch. 3 - Prob. 13PCh. 3 - Prob. 14PCh. 3 - Prob. 15PCh. 3 - Prob. 16PCh. 3 - Prob. 17PCh. 3 - Prob. 18PCh. 3 - HF has equilibrium bond length of 0.926 A and bond...Ch. 3 - Prob. 20PCh. 3 - For each of the following atoms or ions, state the...Ch. 3 - Prob. 22PCh. 3 - Use the data in Figure 3.11 and Table 3.2 to...Ch. 3 - Use the data in Figure 3.11 and Table 3.2 to...Ch. 3 - Prob. 25PCh. 3 - In a gaseous RbF molecule, the bond length is...Ch. 3 - The bond lengths of the XH bonds in NH3,PH3 , and...Ch. 3 - Arrange the following covalent diatomic molecules...Ch. 3 - The bond length in HI(1.62) is close to the sum of...Ch. 3 - Prob. 30PCh. 3 - Use electronegativity values to arrange the...Ch. 3 - Use electronegativity values to rank the bonds in...Ch. 3 - Prob. 33PCh. 3 - Prob. 34PCh. 3 - Prob. 35PCh. 3 - Estimate the percent ionic character of the bond...Ch. 3 - The percent ionic character of a bond can be...Ch. 3 - The percent ionic character of the bonds in...Ch. 3 - Assign formal charges to all atoms in the...Ch. 3 - Assign formal charges to all atoms in the...Ch. 3 - Determine the formal charges on all the atoms in...Ch. 3 - the formal charges on all the atoms in the...Ch. 3 - Prob. 43PCh. 3 - In each of the following Lewis diagrams, Z...Ch. 3 - Draw Lewis electron dot diagrams for the following...Ch. 3 - Prob. 46PCh. 3 - Prob. 47PCh. 3 - Acetic acid is the active ingredient of vinegar....Ch. 3 - Under certain conditions, the stable form of...Ch. 3 - White phosphorus (P4) consists of four phosphorus...Ch. 3 - Draw Lewis electron dot diagrams for the following...Ch. 3 - Draw Lewis electron dot diagrams for the following...Ch. 3 - Draw Lewis diagrams for the two resonance forms of...Ch. 3 - Draw Lewis diagrams for the three resonance forms...Ch. 3 - Methyl isocyanate, which was involved in the...Ch. 3 - Prob. 56PCh. 3 - Draw Lewis diagrams for the following compounds....Ch. 3 - Draw Lewis diagrams for the following ions. In the...Ch. 3 - Prob. 59PCh. 3 - Prob. 60PCh. 3 - For each of the following molecules or molecular...Ch. 3 - For each of the following molecules or molecular...Ch. 3 - Give an example of a molecule or ion having a...Ch. 3 - Give an example of a molecule or ion having a...Ch. 3 - For each of the answers in Problem 59, state...Ch. 3 - For each of the answers in Problem 60, state...Ch. 3 - Prob. 67PCh. 3 - Mixing SbCl3 and GaCl3 in a 1:1 molar ratio (using...Ch. 3 - (a) Use the VSEPR theory to predict the structure...Ch. 3 - Ozone (O3) has a nonzero dipole moment. In the...Ch. 3 - Assign oxidation numbers to the atoms in each of...Ch. 3 - Prob. 72PCh. 3 - Prob. 73PCh. 3 - Prob. 74PCh. 3 - Prob. 75PCh. 3 - Prob. 76PCh. 3 - Prob. 77PCh. 3 - Prob. 78PCh. 3 - Prob. 79PCh. 3 - Prob. 80PCh. 3 - Prob. 81PCh. 3 - Prob. 82PCh. 3 - Prob. 83PCh. 3 - Prob. 84PCh. 3 - Prob. 85APCh. 3 - Prob. 86APCh. 3 - At large interatomic separations, an alkali halide...Ch. 3 - Prob. 88APCh. 3 - Prob. 89APCh. 3 - Two possible Lewis diagrams for sulfine (H2CSO)...Ch. 3 - There is persuasive evidence for the brief...Ch. 3 - The compound SF3N has been synthesized. (a) Draw...Ch. 3 - Prob. 93APCh. 3 - The molecular ion S3N3 has the cyclic structure ...Ch. 3 - Prob. 95APCh. 3 - Prob. 96APCh. 3 - Prob. 97APCh. 3 - Prob. 98APCh. 3 - A stable triatomic molecule can be formed that...Ch. 3 - The gaseous potassium chloride molecule has a...Ch. 3 - (a) Predict the geometry of the SbCl52 ion, using...Ch. 3 - Prob. 102APCh. 3 - Predict the arrangement of the atoms about the...Ch. 3 - Prob. 104APCh. 3 - Prob. 105APCh. 3 - Prob. 106APCh. 3 - Prob. 107APCh. 3 - Prob. 108APCh. 3 - (a) Determine the oxidation number of lead in each...Ch. 3 - Prob. 110APCh. 3 - Prob. 111CPCh. 3 - Prob. 112CPCh. 3 - A compound is being tested for use as a rocket...Ch. 3 - Prob. 114CP
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- Use the References to access important values if needed for this question. What is the IUPAC name of each of the the following? 0 CH3CHCNH₂ CH3 CH3CHCNHCH2CH3 CH3arrow_forwardYou have now performed a liquid-liquid extraction protocol in Experiment 4. In doing so, you manipulated and exploited the acid-base chemistry of one or more of the compounds in your mixture to facilitate their separation into different phases. The key to understanding how liquid- liquid extractions work is by knowing which layer a compound is in, and in what protonation state. The following liquid-liquid extraction is different from the one you performed in Experiment 4, but it uses the same type of logic. Your task is to show how to separate apart Compound A and Compound B. . Complete the following flowchart of a liquid-liquid extraction. Handwritten work is encouraged. • Draw by hand (neatly) only the appropriate organic compound(s) in the boxes. . Specify the reagent(s)/chemicals (name is fine) and concentration as required in Boxes 4 and 5. • Box 7a requires the solvent (name is fine). • Box 7b requires one inorganic compound. • You can neatly complete this assignment by hand and…arrow_forwardb) Elucidate compound D w) mt at 170 nd shows c-1 stretch at 550cm;' The compound has the ff electronic transitions: 0%o* and no a* 1H NMR Spectrum (CDCl3, 400 MHz) 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppm 13C{H} NMR Spectrum (CDCl3, 100 MHz) Solvent 80 70 60 50 40 30 20 10 0 ppm ppm ¹H-13C me-HSQC Spectrum ppm (CDCl3, 400 MHz) 5 ¹H-¹H COSY Spectrum (CDCl3, 400 MHz) 0.5 10 3.5 3.0 2.5 2.0 1.5 1.0 10 15 20 20 25 30 30 -35 -1.0 1.5 -2.0 -2.5 3.0 -3.5 0.5 ppm 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppmarrow_forward
- Part I. a) Elucidate the structure of compound A using the following information. • mass spectrum: m+ = 102, m/2=57 312=29 • IR spectrum: 1002.5 % TRANSMITTANCE Ngg 50 40 30 20 90 80 70 60 MICRONS 5 8 9 10 12 13 14 15 16 19 1740 cm M 10 0 4000 3600 3200 2800 2400 2000 1800 1600 13 • CNMR 'H -NMR Peak 8 ppm (H) Integration multiplicity a 1.5 (3H) triplet b 1.3 1.5 (3H) triplet C 2.3 1 (2H) quartet d 4.1 1 (2H) quartet & ppm (c) 10 15 28 60 177 (C=0) b) Elucidate the structure of compound B using the following information 13C/DEPT NMR 150.9 MHz IIL 1400 WAVENUMBERS (CM-1) DEPT-90 DEPT-135 85 80 75 70 65 60 55 50 45 40 35 30 25 20 ppm 1200 1000 800 600 400arrow_forward• Part II. a) Elucidate The structure of compound c w/ molecular formula C10 11202 and the following data below: • IR spectra % TRANSMITTANCE 1002.5 90 80 70 60 50 40 30 20 10 0 4000 3600 3200 2800 2400 2000 1800 1600 • Information from 'HAMR MICRONS 8 9 10 11 14 15 16 19 25 1400 WAVENUMBERS (CM-1) 1200 1000 800 600 400 peak 8 ppm Integration multiplicity a 2.1 1.5 (3H) Singlet b 3.6 1 (2H) singlet с 3.8 1.5 (3H) Singlet d 6.8 1(2H) doublet 7.1 1(2H) doublet Information from 13C-nmR Normal carbon 29ppm Dept 135 Dept -90 + NO peak NO peak 50 ppm 55 ppm + NO peak 114 ppm t 126 ppm No peak NO peak 130 ppm t + 159 ppm No peak NO peak 207 ppm по реак NO peakarrow_forwardCould you redraw these and also explain how to solve them for me pleasarrow_forward
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