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. |