CBI 1: Fundamentals of Chemistry Part 1 Flashcards

1
Q

Define Atom

A
  • the smallest particle of an element that still retains the identity of a given chemical element
  • an atom comprises of a central nucleus, surrounded by electrons
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2
Q

Define element

A
  • a species of atom all with the same number of protons in the atomic nucleus
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3
Q

Define isotope

A
  • atoms of an element that have the same atomic number, but differ in the number of neutrons
  • therefore having a different atomic mass number
  • isotopes contain the same number of electrons, and therefore exhibit similar chemistry
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4
Q

Define period (of the periodic table)

A
  • elements int he same period contain the same number of electron shells, but differing numbers of valence electrons
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5
Q

Define group (of the periodic table)

A
  • elements that have the same number of valence electrons
  • elements in the same group exhibit similar chemical properties
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6
Q

Define the Pauli exclusion principle

A

No two electrons can have the same set of the four quantum numbers

  • therefore, if principle, orbital and magnetic are the same, then spin number is different
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7
Q

Define the aufbau principle

A
  • the orbitals of lower energy are filled in first with the electrons and only then the orbitals of high energy are filled
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8
Q

Define molecule

A
  • an electrically neutral entity consisting of more than one atom
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9
Q

What is the unified atomic mass unit (u) ?

A
  • also known as Dalton (Da)
  • 1/12 of the mass of an atom of carbon-12
  • which is approximately the mass of a proton or a neutron (1.66 x 10 -27 kg)
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10
Q

What properties demonstrate periodicity?

A
  • Ionization energy:
  • The first ionisation energy is the energy required to eject an electron out of a neutral atom or molecule in its ground state. Subsequent ionization energies relate to the energy required to eject additional electrons.
  • Electronegativity:
  • The power of an atom to attract electrons to itself.
  • Electron affinity:
  • A measure of the energy change that occurs when an additional electron is attached to a neutral atom.
  • Atomic radius:
  • A measure of the distance from the centre of an atomic nucleus to the outermost shell of electron in an atom
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11
Q

Describe the Rutherford-Bohr model of the Atom

A
  • Describes the hydrogen atom with a positively charged nucleus which lies at the centre of the atom surrounded by negatively charged electrons in specific orbits
  • This sought to reconcile observations relating to atomic spectroscopy and limitations of previous ‘planetary’ models and represents the first non-classic atomic model
  • It represented a major advance in understanding of atomic structure and explaining empirical findings
  • But had a number of limitations: primarily couldn’t be used to make accurate predictions for atoms with more than one electron
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12
Q

Describe the Quantum Mechanical Model of the atom

A
  • Erwin Schrodinger suggested that electrons do not orbit the atomic nucleus in a rigidly-defined circular orbits, but that there was some probability associated with them being at a particular distance from the nucleus, that could be described as a mathematical function
  • A quantum mechanical model of the atom explains the behaviour of electrons as waves:
  1. Electrons can be considered to have wave-like properties (matter waves), specifically standing waves.
  2. The allowed behavior of matter waves can be described by the Schrödinger wave equation.
  3. Solutions of this wave equation are known as wave functions and can be used to describe the probability density, which describes the probability of an electron being found at a particular point in space in/around an atom.
  4. Solving the wave equation for electrons with different amounts of energy produces a set of probablity densities for a given atom.
  5. Chemists define the region in an atom that encloses where the electron is likely to be 90% of the time as an atomic orbital.
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13
Q

Define atomic orbital

A
  • a region in an atom where there is a high probability of finding an electron
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14
Q

What are the four types of quantum numbers and what do they describe?

A
  • the four quantum numbers are:
  • Principal (n)
  • Orbital (or azimuthal) (l)
  • Magnetic (ml)
  • Spin (ms)
  • quantum numbers describe the size, shape and number of atomic orbitals and the electrons they contain
  • no two electrons within an atom can have the same set of these four quantum numbers
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15
Q

What is the principle quantum number (n) ?

A
  • Specifies the ‘shell’
  • N = 1, 2, 3 etc
  • Specifies the size of the orbital
  • Orbitals with a larger number extend further from the nucleus and have higher energies (less tightly bound)
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16
Q

What is the orbital quantum number(l) ?

A
  • Specifies the subshell and determines the set of shapes the orbital can take
  • Values can be: l = 0, 1, 2 … (n-1) where n is the principal quantum number
  • Subshells denoted by the letters: s, p, d, f, g…
  • L = 0 denoted by s
  • L = 1 denoted by p
  • L = 2 denoted by d
  • L = 3 denoted by f
  • Depending on the value of l, orbitals have different shapes
    • S-orbitals are spherical
    • P-orbitals are a pair of drop-shaped lobes on opposing sides of the nucleus
    • D-orbitals are also lobed
    • F-orbitals have multiple sets of lobes
  • The third principle shell (n=3) has three subshells denoted by s, p, d corresponding to l = 0, 1, 2
17
Q

What is the magnetic quantum number?

A
  • specifies the possible orientation of the orbital shapes
18
Q

What is the spin quantum number?

A
  • Dictates that each of the orbitals can house two electrons and no more
  • Can take one of two values:
    • –½
  • Electrons in orbitals obey the Pauli exclusion principle which is:
    • No two electrons can have the same set of the four quantum numbers
19
Q

Describe how orbitals are occupied in the atom

A
  • there can be a max of two electrons in one orbital
  • Each must have opposite spin (Pauli exclusion principle)
  • Electrons occupy the lowest energy orbital first (aufbau principle):
    • The orbitals of lower energy are filled in first with the electrons and only then the orbitals of high energy are filled
  • Electrons only pair up if there is no orbital of the same energy available (Hund’s rule)
    • Negatively-charged electrons repel each other and will try to occupy regions of available space that are as far away as is possible (I.e. different degenerate subshells) before they have to occupy the same atomic orbital by pairing up
20
Q

What is Hund’s Rule?

A

Electrons will fill separate orbitals in the same subshell before pairing up, and unpaired electrons will have the same spin.

21
Q

What is the Mandelung Rule?

A
  • At higher energy levels (n>3), the orbital energies begin to overlap
  • 4s < 3d so 4s is filled up first
22
Q

Describe ionic bonding

A
  • Look through e-module
23
Q

Describe covalent bonding

A
  • Look through e-module
24
Q

What causes a polar covalent bond?

A
25
Q

What is VSEPR theory used for and what does it stand for?

A
26
Q

Describe the typical geometrical arrangements with different electron regions

A
27
Q

What are the two theories in which chemical bonding is explained?

A
  • Valence Bond theory (VB)
  • Molecular Orbital (MO) theory
28
Q

Describe Valence Bond (VB) theory

A

Two key concepts:

  1. Overlap of Atomic Orbitals:
    - the bonding electrons are localised in the region of atomic orbital overlap
  2. Hybridisation:
    - there may be hybrid character between several possible types of orbitals
29
Q

Explain the types of bonding atomic orbital overlaps cause

A
  • For each covalent bond, there is a condition of maximum overlap that leads to maximum bond strength
  • For atomic orbitals with directional lobes (p, d, f) the maximum overlap will occur when atomic orbitals overlap end-to-end, along the bond axis
  • Sigma bonds are formed by the end-to-end overlap of s, p, d, f orbitals
  • Pi-bonds are formed when p, d, or f orbitals overlap sideways (I.e. parallel) to sigma-bonds
    • The overlap is less and the bond is weaker
    • The overlap is not occurring directly along the axis, but parallel to it
    • Pi-bonds prevent free rotation around the axis
30
Q

Explain the problem hybridisation solves using carbon as an example

A
31
Q

Describe orbital hybridization

A
  • Involves combining the atomic orbitals in the valence shell to make a new set of orbitals that includes hybridized orbitals
  • In methane, the carbon is bonded to four H atoms and orbital hybridization explains how the 2s atomic orbital and the three 2p orbitals combine to form four new sp3 hybridized orbitals
  • These are energetically equivalent (we say that they are degenerate) and each can contain one of the four valence electrons in carbon
  • We can now overlap these hybridized orbitals to make four covalent bonds
  • As they are degenerate, the sp3 hybridized orbitals point to the corners of a tetrahedron; one part s-character and three parts p-character
  • The number of hybrid orbitals is equal to the total number of orbitals
32
Q

State the type of hybridization in these atoms and draw their electronic configuration:

  • nitrogen
  • oxygen
  • beryllium
  • boron
A
33
Q

How does valence bonding explain the character of double and triple bonds?

A
34
Q

Describe the type of hybridization in carbon double and triple bonds and their configuration

A
35
Q

Explain how double bonds can form in ethylene

A
36
Q

Explain how triple bonds can form acetylene

A
37
Q

Describe molecular orbital (MO) theory

A
  • An alternative to VB theory
  • One of the differences is that MO assumes there are empty orbitals
  • Molecular spectroscopy techniques provide evidence on the existence of these
  • MO theory already implies that molecular orbitals are delocalised over the molecule
  • MO theory can predict accurately bond lengths and bond energies – useful for molecular modelling
  • Major drawback is that for large molecules, the theory get horrendously complex