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(a)
Interpretation:
Whether the molecule dimethylacetylene,
Concept introduction:
Nonlinear molecules can rotate in three independent and mutually perpendicular directions. It is not necessary that the rotation in one dimension is equivalent to rotations in the other two directions. The moment of inertia for each dimension of each rotation is usually different. If a molecule has three different moments of inertia, it is called an asymmetric top molecule. If a molecule has two of its three moments of inertia equal, it is called symmetric top molecule. If the two equal moments of inertia are lower than the unique moment of inertia, then the molecule is called oblate tops. If the two equal moments of inertia are higher than the unique moment of inertia, then the molecule is called prolate tops. For linear molecule, the moment of inertia along the molecular axis is zero. Spherical top molecules have no net dipole moment or net dipole moment is equal to zero.
(b)
Interpretation:
Whether the molecule sulfur hexafluoride,
Concept introduction:
Nonlinear molecules can rotate in three independent and mutually perpendicular directions. It is not necessary that the rotation in one dimension is equivalent to rotations in the other two directions. The moment of inertia for each dimension of each rotation is usually different. If a molecule has three different moments of inertia, it is called an asymmetric top molecule. If a molecule has two of its three moments of inertia equal, it is called symmetric top molecule. If the two equal moments of inertia are lower than the unique moment of inertia, then the molecule is called oblate tops. If the two equal moments of inertia are higher than the unique moment of inertia, then the molecule is called prolate tops. For linear molecule the moment of inertia along the molecular axis is zero. Spherical top molecules have no net dipole moment or net dipole moment is equal to zero.
(c)
Interpretation:
Whether the molecule phosphate ion,
Concept introduction:
Nonlinear molecules can rotate in three independent and mutually perpendicular directions. It is not necessary that the rotation in one dimension is equivalent to rotations in the other two directions. The moment of inertia for each dimension of each rotation is usually different. If a molecule has three different moments of inertia, it is called an asymmetric top molecule. If a molecule has two of its three moments of inertia equal, it is called symmetric top molecule. If the two equal moments of inertia are lower than the unique moment of inertia, then the molecule is called oblate tops. If the two equal moments of inertia are higher than the unique moment of inertia, then the molecule is called prolate tops. For linear molecule the moment of inertia along the molecular axis is zero. Spherical top molecules have no net dipole moment or net dipole moment is equal to zero.
(d)
Interpretation:
Whether the molecule glycine,
Concept introduction:
Nonlinear molecules can rotate in three independent and mutually perpendicular directions. It is not necessary that the rotation in one dimension is equivalent to rotations in the other two directions. The moment of inertia for each dimension of each rotation is usually different. If a molecule has three different moments of inertia, it is called an asymmetric top molecule. If a molecule has two of its three moments of inertia equal, it is called symmetric top molecule. If the two equal moments of inertia are lower than the unique moment of inertia, then the molecule is called oblate tops. If the two equal moments of inertia are higher than the unique moment of inertia, then the molecule is called prolate tops. For linear molecule the moment of inertia along the molecular axis is zero. Spherical top molecules have no net dipole moment or net dipole moment is equal to zero.
(e)
Interpretation:
Whether the molecule cis
Concept introduction:
Nonlinear molecules can rotate in three independent and mutually perpendicular directions. It is not necessary that the rotation in one dimension is equivalent to rotations in the other two directions. The moment of inertia for each dimension of each rotation is usually different. If a molecule has three different moments of inertia, it is called an asymmetric top molecule. If a molecule has two of its three moments of inertia equal, it is called symmetric top molecule. If the two equal moments of inertia are lower than the unique moment of inertia, then the molecule is called oblate tops. If the two equal moments of inertia are higher than the unique moment of inertia, then the molecule is called prolate tops. For linear molecule the moment of inertia along the molecular axis is zero. Spherical top molecules have no net dipole moment or net dipole moment is equal to zero.
(f)
Interpretation:
Whether the molecule trans
Concept introduction:
Nonlinear molecules can rotate in three independent and mutually perpendicular directions. It is not necessary that the rotation in one dimension is equivalent to rotations in the other two directions. The moment of inertia for each dimension of each rotation is usually different. If a molecule has three different moments of inertia, it is called an asymmetric top molecule. If a molecule has two of its three moments of inertia equal, it is called symmetric top molecule. If the two equal moments of inertia are lower than the unique moment of inertia, then the molecule is called oblate tops. If the two equal moments of inertia are higher than the unique moment of inertia, then the molecule is called prolate tops. For linear molecule the moment of inertia along the molecular axis is zero. Spherical top molecules have no net dipole moment or net dipole moment is equal to zero.
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Chapter 14 Solutions
Physical Chemistry
- Draw the Lewis structure of C2H4Oarrow_forwarda) 5. Circle all acidic (and anticoplanar to the Leaving group) protons in the following molecules, Solve these elimination reactions, and identify the major and minor products where appropriate: 20 points + NaOCH3 Br (2 productarrow_forwardNonearrow_forward
- Dr. Mendel asked his BIOL 260 class what their height was and what their parent's heights were. He plotted that data in the graph below to determine if height was a heritable trait. A. Is height a heritable trait? If yes, what is the heritability value? (2 pts) B. If the phenotypic variation is 30, what is the variation due to additive alleles? (2 pts) Offspring Height (Inches) 75 67.5 60 52.5 y = 0.9264x + 4.8519 55 60 65 MidParent Height (Inches) 70 75 12pt v V Paragraph B IUA > AT2 v Varrow_forwardExperiment: Each team will be provided with 5g of a mixture of acetanilide and salicylic acid. You will divide it into three 1.5 g portions in separate 125 mL Erlenmeyer flasks savıng some for melting point analysis. Dissolve the mixture in each flask in ~60mL of DI water by heating to boiling on a hotplate. Take the flasks off the hotplate once you have a clear solution and let them stand on the bench top for 5 mins and then allow them to cool as described below. Sample A-Let the first sample cool slowly to room temperature by letting it stand on your lab bench, with occasional stirring to promote crystallization. Sample B-Cool the second sample 1n a tap-water bath to 10-15 °C Sample C-Cool the third sample in an ice-bath to 0-2 °C Results: weight after recrystalization and melting point temp. A=0.624g,102-115° B=0.765g, 80-105° C=1.135g, 77-108 What is the percent yield of A,B, and C.arrow_forwardRel. Intensity Q 1. Which one of the following is true of the compound whose mass spectrum is shown here? Explain how you decided. 100 a) It contains chlorine. b) It contains bromine. c) It contains neither chlorine nor bromine. 80- 60- 40- 20- 0.0 0.0 TT 40 80 120 160 m/z 2. Using the Table of IR Absorptions how could you distinguish between these two compounds in the IR? What absorbance would one compound have that the other compound does not? HO CIarrow_forward
- Illustrate reaction mechanisms of alkenes with water in the presence of H2SO4, detailing each step of the process. Please show steps of processing. Please do both, I will thumb up for sure #1 #3arrow_forwardDraw the following molecule: (Z)-1-chloro-1-butenearrow_forwardIdentify the molecule as having a(n) E, Z, cis, or trans configuration. CH3 H₁₂C ○ E ○ z ○ cis transarrow_forward
- Identify the molecule as having a(n) E, Z, cis, or trans configuration. H₂C- CH3 О Е ○ cis ○ transarrow_forwardThe decomposition of dinitrogen pentoxide according to the equation: 50°C 2 N2O5(g) 4 NO2(g) + O2(g) follows first-order kinetics with a rate constant of 0.0065 s-1. If the initial concentration of N2O5 is 0.275 M, determine: the final concentration of N2O5 after 180 seconds. ...arrow_forwardDon't used hand raitingarrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningGeneral Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage Learning
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