PHYSICAL CHEMISTRY: true/false – Flashcards
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Electron diffraction is one physical observation that lead to the discovery of quantum mechanics
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true
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Quantization of energy is an important observation for atomic and molecular scale systems
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true
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Blackbody radiation cannot be explained by classical mechanics
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true
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A wave function tells the amplitude of a wave function as a function of time but not position
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false
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In quantum mechanics, physical observables each have a corresponding operator
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true
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Whether quantum mechanics is necessary to describe a system is based on the degree to which allowed energy values form a continuous spectrum
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true
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An operator always operates on the function to its left
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false: to its right
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A group of functions labeled a complete set can be combined to describe any state
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true
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The Schrodinger equation generates a family of wave functions that are orthogonal to each other
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true
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Postulates are the foundation of a theory
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true
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Operators always form an eigenfunction/eigenvalue relationship with the wave functions of the Schrodinger equation
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false
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The particle in a box system has wavefunctions that are not continuous at the sides of the box
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false
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Despite infinite potential energy outside, the particle of a box in a boxy system has a nonzero probability of being outside the box
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false
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The probability of finding the particle in a particle in a box system does not depend on what part of the box you are looking at
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false
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The particle in a box system can also be considered in 2 and 3 dimensions
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true
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The energy levels of a particle in an infinite box are farther apart for a heavier particle
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false
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Particles in a box with finite potential energy walls have no probability of being outside the box
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false
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The higher in kinetic energy of a state, the less likely it will be in a classically forbidden area
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false
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Reactions involving quantum mechanical tunneling have a higher probability for lighter atoms
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true
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Boundary conditions, initial conditions and normalization are important in determining specific wave functions
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true
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Odd functions satisfy the relationship: f(-x)=-f(x)
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true
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the potential energy of the rigid rotor system has the form: kx^2/2
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false
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Harmonic oscillator wave functions have a non-zero probability of being in classically forbidden region
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true
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Rotational energy levels are further apart in energy than vibrational energy levels
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false
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The distinct energy levels described by quantum mechanics make spectroscopy a good way to identify molecules
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true
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Spectroscopy depends on interaction of oscillating electric fields from EM radiation and matter
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true
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Spontaneous absorption of light moves a system to a higher energy state
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true
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The harmonic oscillator model is best for describing low quantum number vibrational states
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true
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Rotational spectroscopy is often used by organic chemists to identify functional groubs
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false: vibrational spectroscopy
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The width of infrared absorptions is due to transitions occurring in rotational states within vibrational states
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true
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The electrons around atoms are best described using quantum mechanics
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true
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The principle quantum number of a hydrogen orbital can be determined by its shape (spherical, dumbell)
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false
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The energy of the hydrogen atom wavefunctions depends primarily on the principle quantum number, n
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true
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An orbital is defined as a multielectron wavefunction
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false: a single electron wavefunction
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The electrons of the helium atom are described well by the hydrogen atom wave functions and changing the nuclear charge
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false
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In the quantum mechanical treatment of atoms we assumed the nucleus was immobile (the nucleus does not move)
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true
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Electron spin is a direct result of the Schrodinger equation
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false
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Variational method is the most common approximation method to solve Schrodinger equation
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true
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Matrices are used to represent wave functions and include electron spin
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True
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Variational parameters are optimized when they maximize the energy of the trial wave function
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false: when they minimize the energy of the trial wavefunction
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Molecular orbitals are more often written as a linear combination of atomic orbitals
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true
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A basis set is a collection of wavefunctions used to approximate a wavefunction that cannot be solved for exactly
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true
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The hartree-fock method provides a way to determine molecular orbitals without applying any approximation
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false
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For every bonding orbital that is formed an antibonding orbital is formed
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true
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Bonding orbitals have a higher energy than the atomic orbitals that combine to make the bonding orbital
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false