| a. waves. | ||
| b. both waves and particles. | ||
| c. particles. | ||
| d. none of these choices. |
| a. waves. | ||
| b. particles. | ||
| c. both waves and particles. | ||
| d. none of these choices. |
| a. light diffraction. | ||
| b. the photoelectric effect. | ||
| c. color. | ||
| d. interference effects. |
| a. diffraction. | ||
| b. the photoelectric effect. | ||
| c. blackbody radiation. | ||
| d. absorption of light by an electron. |
| a. 2 | ||
| b. 1 | ||
| c. 4 | ||
| d. 3 |
| a. 3 | ||
| b. 5 | ||
| c. 4 | ||
| d. 1 |
| a. that electrons have momentum. | ||
| b. that electrons have mass. | ||
| c. the diffraction of electrons. | ||
| d. that electrons are attracted to the nucleus in an atom. |
| a. the wavelength of green light. | ||
| b. the photoelectric effect. | ||
| c. color of light. | ||
| d. intensity of light. |
| a. 4.733 x 10^(-33) m | ||
| b. 8.451 x 10^(33) m | ||
| c. 1.183 x 10^(-34) m | ||
| d. 1.657 x 10^(-35) m |
| a. 1.380 x 10^(-39) m | ||
| b. 6.599 x 10^(8) m | ||
| c. 7.273 x 10^(-4) m | ||
| d. 1.515 x 10^(-9) m |
| a. 3.300 x 10^(18) J | ||
| b. 3.030 x 10^(-19) J | ||
| c. 1.010 x 10^(-27) J | ||
| d. 4.573 x 10^(14) J |
| a. 6.912 x 10^(14) J | ||
| b. 1.526 x 10^(-27) J | ||
| c. 4.580 x 10^(-19) J | ||
| d. 2.180 x 10^(18) J |
| a. momentum. | ||
| b. Laplacian. | ||
| c. Hamiltonian. | ||
| d. Hermitian. |
| a. Single valued | ||
| b. Finite | ||
| c. Continuous | ||
| d. All of these choices |
| a. positive everywhere. | ||
| b. normalizable. | ||
| c. reliable. | ||
| d. none of these choices. |
| a. the Heisenberg uncertainty principle. | ||
| b. zero-point energy. | ||
| c. quantization of energy. | ||
| d. all of these choices. |
| a. quantization of energy. | ||
| b. the Heisenberg uncertainty principle. | ||
| c. zero-point energy. | ||
| d. all of these choices. |
| a. quantization. | ||
| b. quantum mechanical tunneling. | ||
| c. normalization. | ||
| d. zero-point energy. |
| a. It occurs in the harmonic oscillator system. | ||
| b. It is the phenomenon that wave functions can extend into the classically forbidden region, i.e., the region where a classical particle would have negative kinetic energy. | ||
| c. It becomes less as the mass of particle increases. | ||
| d. All of these choices |
| a. 2.87 x 10^(-22) J | ||
| b. 5.74 x 10^(-20) J | ||
| c. 0 | ||
| d. 2.87 x 10^(-20) J |
| a. 0 | ||
| b. 5.08 x 10^(-20) J | ||
| c. 2.54 x 10^(-20) J | ||
| d. 1.27 x 10^(-20) J |
| a. is a constant. | ||
| b. increases as the quantum number becomes larger. | ||
| c. decrease as the quantum number becomes larger. | ||
| d. none of these choices. |
| a. three angular nodes and one radial node. | ||
| b. four angular nodes and two radial nodes. | ||
| c. four angular nodes and one radial node. | ||
| d. two angular nodes and one radial node. |
| a. two angular nodes and two radial nodes. | ||
| b. one angular nodes and three radial nodes. | ||
| c. five angular nodes and three radial nodes. | ||
| d. one angular node and five radial nodes. |
| a. (2, 2, 1), (2, 1, -1), (2, 1, 0), (2, 1, 1), and (2, 0, 0). | ||
| b. (2, 1, -1), (2, 1, 0), (2, 1, 1), and (2, 0, 0). | ||
| c. (2, 1, -1), (2, 1, 0), (2, 1, 1), (2, 0, -1), (2, 0, 0), and (2, 0, 1). | ||
| d. (2, 2, -1), (2, 1, -1), (2, 1, 0), and (2, 1, 1). |
| a. 3. | ||
| b. 3.5. | ||
| c. 2. | ||
| d. 2.5. |
| a. 8.63 kcal/mol | ||
| b. 43.17 kcal/mol | ||
| c. 25.90 kcal/mol | ||
| d. 17.27 kcal/mol |
| a. 7.65 kcal/mol | ||
| b. 22.96 kcal/mol | ||
| c. 15.30 kcal/mol | ||
| d. 38.26 kcal/mol |
| a. pure rotational transition. | ||
| b. pure vibrational transition. | ||
| c. electronic transition. | ||
| d. none of these choices. |
| a. Pure rotational transition | ||
| b. Pure vibrational transition | ||
| c. Electronic transition | ||
| d. Ro-vibrational transition |
| a. J = 4 to J = 3 | ||
| b. J = 1 to J = 0 | ||
| c. J = 3 to J = 4 | ||
| d. J = 0 to J = 1 |
| a. J = 4 to J = 3 | ||
| b. J = 0 to J = 1 | ||
| c. J = 3 to J = 4 | ||
| d. J = 4 to J = 5 |
| a. Electronic transition | ||
| b. Rotational transition | ||
| c. Vibrational transition | ||
| d. Translational transition |
| a. Rotational transition | ||
| b. Ro-vibrational transition | ||
| c. Vibrational transition | ||
| d. Electronic transition |
| a. Fluorescence | ||
| b. Phosphorescence | ||
| c. Transference of energy to a nearby receptor molecule | ||
| d. All of these choices |
| a. Absorption of light by the vibrational transition obeys the Franck-Condon principle. | ||
| b. The ground electronic state has very similar vibrational states as the first electronic excited state. | ||
| c. The emission of light by vibrational transition obeys the Franck-Condon principle. | ||
| d. Both absorption and emission of light are measured by the same instrument. |
| a. Absorption of light from the ground electronic state starts at the ground vibrational state. | ||
| b. Both absorption and emission of light are directly proportional to concentration of the molecule | ||
| c. Emission of light from the electronically excited state starts at the ground vibrational state. | ||
| d. The Franck-Condon principle governs both absorption and emission of light by the molecule. |
| a. All protons align opposite to the field. | ||
| b. Some protons align with the field and some align opposite to it. | ||
| c. All protons align with the field. | ||
| d. All protons assume a random orientation. |
| a. The RF will force all spins to align opposite to the magnetic field. | ||
| b. The RF will force all spins to assume a random orientation. | ||
| c. The RF will force all spins to align with the magnetic field. | ||
| d. The RF will flip the spin so as to prompt a spin transition to a slightly higher energy state. |