4. Bonding Flashcards

1
Q

Ionic Bonding

A

The electrostatic attraction between oppositely charged ions

  • Cations: positive charge, lose valence electrons (metals)
  • Anions: negative charge, gain valence electrons (non-metals)
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2
Q

Ionic Bond Properties

A
  • non directional bond - strength of bond eaqual in all directions
  • conducts electricity when molten/ in solution
  • high melting/ boiling points
  • hard solids
  • low volatility
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3
Q

Covalent Bonding

A

The electrostatic attraction between a pair of electrons and positively charged nuclei

  • bonding electron pairs
  • electrons not involved in bonding are called non-bonding e- pairs
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4
Q

Electronegativity Difference

A
  • Covalent - high electronegativity locks the electrons in covalent bonds
  • Metalic - Low electronegativity allows electrons to float in seas
  • Ionic - high electronegativity difference means uneven sharing

< 0.4 ——————————————— 1.8<

nonpolar polar ionic

covalent bond covalent bond

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5
Q

Polarity

A
  • Partial positive charge (positive/ negative)
  • The overall charge = Dipole movement
  • The molecular is polar if the electron densities are not symmetrical (eg H2O)
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6
Q

Ionic Bond strength

A
  • electrostatic attraction between positive and negative ions
  • the smaller the ions / the greater the charge on the ions, the stronger the attraction between the ions
    • greater charge density within the structure
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7
Q

Covalent Bond strength

A
  • shared pair of electrons between atoms
  • the shorter the bond, the stronger it is
    • triple bonds are shorter and stronger than double bonds
    • triple > double > single
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8
Q

Metallic Bond strength

A
  • attraction between lattice of positive metal ions and delocalized outer shell electrons
  • the smaller the metal ions, the greater the charge on ions
  • the more delocalised outer shell electrons there are, the stronger the attraction between the ions and electrons
    • greater charge density within the structure
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9
Q

Lewis Structures

A
  • representations of molecules showing all electrons, bonding and nonbinding
  • each bond contains 2 electrons
  • elements pair up according to the octet rule
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10
Q

Exceptions to the Octet rule

A
  • Boron - forms stable compounds with just 3 valence electrons
    • highly reactive
  • Beryllium - forms stable compounds with just 2 valence electrons
  • compounds that break the octet rule are often toxic and dangerous, ready to react so the octet rule is obeyed
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11
Q

VSEPR Theory

A

Valence Shell Electron Pair Repulsion

Electron domain - the number of bonds/ electron pairs there are on the central atom

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12
Q

Shapes w/ non-bonding electron pairs

A

If a molecule / ion has lone pairs on the central atom, the shapes are slightly distorted away from the regular shapes

because of extra repulsion caused by the lone pairs

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13
Q

Shape Angles - Linear

A

180

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14
Q

Shape Angles - Bent

A

105

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15
Q

Shape Angles - Trigonal Planar

A

120

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16
Q

Shape Angles - pyramidal

A

107

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17
Q

Shape Angles - Tetrahedral

A

109.5

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18
Q

Shape Angles - Octahedral

A

90

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19
Q

Resonance structures

A

When a lewis structure allows for the same arrangement of atoms but a different but equally valid arrangement of electrons, resonance occurs

  • Electrons are delocalized and are spread over 2 bonding orbitals
  • Located in the p orbitals - overlapping p orbitals create pi bonds with delocalized electrons
20
Q

Allotropes

A

Compounds of the same element that differ in structure

eg Carbon

21
Q

Diamond (structure & properties)

A
  • Each carbon bonded to 4 other carbons by sp3 hybridization
  • High melting point
    • strong directional covalent bond
  • Extremely hard
    • difficult to break atoms apart/ move them in relation to one another
  • No electrical conductivity
    • electrons are localized in specific bonds
  • Insoluble in polar and non-polar solvents because molecular bonds are stronger than any IMF
22
Q

Graphite (structure)

A
  • Carbon atoms bonded via sp2 hybridization
  • form sheets of 6 sided rings with p-orbitals perpendicular from plane of ringt
    • presence of p orbitals allows for stronger london forces that hold the sheets together
23
Q

Graphite (properties)

A
  • Conducts electricity - delocalized electrons
  • Slippery - sheets can slip past each other
  • High melting point - delocalized electrons
  • Insoluble
24
Q

Fullerenes

A

Buckyballs

  • carbon atoms bond in units of 60 atoms, with interlocking 6 sided and 5 sided rings
  • sp2 hybridization - extra p orbitals form pi bonds resulting in the properties

Properties

  • Super strong
  • conduct electricity and heat with low resistance
  • free radical scavenger
25
Q

Silicon structures

A
  • SiO2 repeating in a tetrahedral structure
  • Si is larger than C so the Si-Si bond length is greater
    • the greater the bond length, the lower the bond enthalpy
    • easier to break
    • more reactive than diamond
26
Q

Intermolecular Forces - London Forces

A
  • between 2 non-polar molecules
  • caused by the motion of electrons around a nucleus
    • creation of temporary dipoles / instantaneous induced dipoles
  • increases with atomic radii
27
Q

Intermolecular Forces - Dipole Dipole Forces

A
  • between 2 polar molecules
    • permanent dipole
  • the partially charged ends of the molecules attract and repel each other
  • LDFs are always acting as well
  • usually asymmetrical molecules
    • except for bent structured molecules eg water
28
Q

Intermolecular Forces - Hydrogen Bonds

A
  • between an electronegative atom from one molecule and a hydrogen atom from another
    • N, O, F
  • super strong dipole dipole bond
  • hydrogen bond 5% stronger than an average covalent bond due to lack of underlying layer of electrons
29
Q

Effect of IMF on Boiling Points

A
  • phase change is when the IMF are overcome
  • liquid turns into a gas when the attractive forces between the particles are completely broken
  • Covalent macromolecular structure - extremely high melting / boiling points
  • Metals/ Ionic compounds - high boiling points due to ionic attractions
  • The weaker the attractive forces, the more volatile the substance
30
Q

Metallic Bonding

A

The electrostatic attraction between a lattice of positive ions and delocalized electrons

  • strength of bond increases with charge of ion
  • conducts electricty - delocalized electrons
  • malleable - close-packed layers of positive ions can slide over each other without breaking more bonds than are made
31
Q

Alloys

A

Mixtures of metals and one or more other elements

Produces increased

  • strength
  • durability
  • hardness
  • resistance to corrosion
  • magnetic properties
    • due to the different elements being of different sizes preventing the easy sliding between 2 atoms
32
Q

Composition of Brass and Steel

A

Brass

Copper and Zinc

Steel

Iron and Carbon

33
Q

Formal Charge (FC)

A

FC = valence e- - 0.5bonding e- - non-binding e-

Most favored Lewis Structure:

Structure with the FC closest to zero

The structure with the negative FC on the most electronegative atom

34
Q

Overlapping Orbitals

A
  • Sigma bonds result from the axial overlap of orbitals
  • Pi bonds result from the sideways overlap of parallel p orbitals
  • double bonds fomed by 1 sigma and 1 pi bond
  • triple bonds formed by 1 sigma and 2 pi bonds
35
Q

Sigma Bonds

A
  • Head to head overlap
  • Cylindrical symmetry of electron density around the internuclear axis
36
Q

Pi Bonds

A
  • Side-to-side overlap
  • Electron density above and below the internuclear axis
  • electron overlap is weaker, yet there is an extra bond –> energy required to break them is more
37
Q

Importance of Ozone

A
  • At ground level reacts with chemicals to form smog, harms respiratory systems and degrades materials
  • At atmospheric levels is essential for life
    • absorbs UV radiation
    • exothermic reactions cause a temp. inversion in the stratosphere –> prevents convection keeping the layers of atmosphere stable
38
Q

Ozone Formation Equation

A

O2(g) + UV (242nm) –> O•(g) + O•(g)

O•(g) + O2(g) –> O3(g)

exothermic

39
Q

Ozone Depletion Equation

A

O3(g) + UV(330nm) –> O2(g) + O•(g)

O3(g) + O•(g) –> 2O2(g)

40
Q

Catalytic Ozone Destruction - Nitrogen Oxides

A

NO•(g) + O3(g) –> NO2(g) + O2(g)

NO2(g) + O• –> NO•(g) + O2(g)

41
Q

Catalytic Ozone Destruction - Chlorofluorocarbons

A

CCl2F2(g) –> CClF2(g) + Cl•(g)

Cl•(g) + O3(g) –> O2(g) + ClO•(g)

ClO•(g) + O•(g) –> O2(g) + Cl•(g)

42
Q

Bond Order

A

The measurement of the number of e- involved in bonds between two atoms in a molecule (if bond order = 0, there is no bonding)

Bond Order = Total bonding pairs / total no. of positions

eg Ozone O3 = 3/2

43
Q

Hybridization (definition)

A

The mixing of different types of orbitals to produce new types of orbitals –> most hybrid orbitals are combinations of s and p orbitals that then form sigma bonds

number of electron domains = amount of hybridization there is

2: sp // 3: sp2 // 4: sp3

44
Q

Two sp orbitals

A
  • Triple bonds
  • 2 sp orbitals form a sigma bond between the carbons, and two pairs of p orbitals overlap to form the 2 pi bonds
45
Q

Three sp orbitals

A
  • sp2 orbital on carbon overlaps to form a sigma bond with the orbital in oxygen
  • the unhybridized p orbitals overlap in pi fashion
46
Q

Four sp orbitals

A
  • sp3 orbitals on carbon overlap to form a sigma bond with orbitals in H