
(a)
Interpretation:
Whether the molecule hexamethylbenzene,
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 diacetylene,
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 cyanide radical,
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 cyanogen,
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 sulfur tetrafluoride,
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 hydrogen sulphide,
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 dimensions 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
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- A mixture of C7H12O2, C9H9OCl, biphenyl and acetone was put together in a gas chromatography tube. Please decide from the GC resutls which correspond to the peak for C7,C9 and biphenyl and explain the reasoning based on GC results. Eliminate unnecessary peaks from Gas Chromatography results.arrow_forwardIs the molecule chiral, meso, or achiral? CI .CH3 H₂C CIarrow_forwardPLEASE HELP ! URGENT!arrow_forward
- Identify priority of the substituents: CH3arrow_forwardHow many chiral carbons are in the molecule? OH F CI Brarrow_forwardA mixture of three compounds Phen-A, Acet-B and Rin-C was analyzed using TLC with 1:9 ethanol: hexane as the mobile phase. The TLC plate showed three spots of R, 0.1 and 0.2 and 0.3. Which of the three compounds (Phen-A; Acet-B or Rin-C) would have the highest (Blank 1), middle (Blank 2) and lowest (Blank 3) spot respectively? 0 CH: 0 CH, 0 H.C OH H.CN OH Acet-B Rin-C phen-A A A <arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher: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

