Topic 2 Flashcards

Bonding, structure + shape of molecule (37 cards)

1
Q

Intramolecular v Intermolecular bonding

What’s a compound?

A

Intramolecular – bonding that takes places when atoms join to other atoms (bonding WITHIN a molecule)
[covalent/ionic/metallic]

Intermolecular – bonding BETWEEN molecules – much weaker than covalent/ionic/metallic
[Van der waals forces, permanent dipole-dipole, hydrogen bonding]

Compound - when different elements join/bond together (2 types of bonding in compounds - covalent + ionic)

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2
Q

Atoms to atoms bonding types

Ionic bonding?
Cations?
Anions?

A
  • The complete transfer of electrons from one atom to another
  • bonding of oppositely charged ions
  • Cations = Positive ions = Atoms which have lost electron = metallic
  • Anions = Negative ions = Atoms which have gained electron = non-metallic
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3
Q

Covalent bonding?

A
  • Electron sharing between non-metallic atoms that are both electron deficient in their outer orbitals
  • Only way to achieving full outer shell is by sharing their electrons
  • A shared pair of electrons where each atom donates one electron

dot + cross diagrm used

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4
Q

Dative covalent bonding / coordinate bonding

A
  • special case of covalent bond where 1 atom donates BOTH electrons that form the shared bond pair
  • A shared pair of electrons where one atom donates both electrons
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5
Q

Metallic bonding

A
  • bonding in metals, metal atoms lose their outer electron to gain stability+become positive ions (cations)
  • +the electrons become delocalised (not fixed in 1 place but are free to move around) + move around this structure of cations, holding it together through electrostatic attraction
  • metallic bonding refers to the strong electrostatic forces of attraction between the positively charged metal ions + the “sea” of delocalized electrons that surround them
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6
Q

What does electronegativity of an atom mean?

A
  • The electronegativity of an atom is the ability of its nucleus to attract electrons in a bond pair
  • EN explans different bondings
  • If the EN difference is 0 (the same atoms eg Cl – Cl) there will be a pure covalent bond
  • If the EN difference is very large there will be a complete transfer of electrons causing an ionic bond
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7
Q

Polar v non-polar covalent bonds

A
  • Polar bond = covalent bond between atoms of different electronegativities = the bonding electrons will be pulled towards the more EN atom =makes bond polar
  • In a polar bond, the difference in EN between 2 atoms causes a permanent dipole = difference in charge between 2 atoms caused by a shift in electron density in bond
  • Non-polar =covalent bond between 2 atoms of the same element (H2) is non-polar as they have equal electronegativities = e- are equally attracted to both nuclei
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8
Q

Intermediate bonds

Polarization of anions

A
  • pure ionic compounds have ions which are perfectly spherical
  • If there’s a large difference in charge / density between the cation + anion = the anion (because of its extra electron cloud) becomes distorted by the pull of the cation = polarization of the anion
  • Polarization = Distortion of anion’s electron cloud by a nearby cation
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9
Q

Fajan’s rules explain effect of ion size + ion charge in this situation

A
  • Either the anion/cation is highly charged (it would make the cations highly polarising + the anion highly polarisable)
  • the cation is small (so it will have a high charge density)
  • the anion is large (so the e- are far from the nucleus = less under its control)
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10
Q

What’s a a polar covalent molecule

A
  • A molecule in which the electrons are shared unequally between 2 atoms due to a difference in their electronegativities
  • This unequal sharing creates a dipole moment, where one end of the molecule has a partial positive charge (δ⁺) + the other end has a partial negative charge (δ⁻)
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11
Q

Inter-molecular forces [3 types]

  1. Permanent dipole
A
  • Dipole attraction = the negative part of one molecule is attracted to the positive part of another, hence there is a bond between the molecules
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12
Q
  1. Hydrogen bonding?
A
  • occurs when a hydrogen atom [the δ+] covalently bonded to a highly electronegative atom [the δ-] (such as nitrogen, oxygen or fluorine) interacts with another electronegative atom to from H bonds
  • The high EN difference results in the N, O or F atom having a much greater “share” of the electrons than the H atom
  • The O, N or F atom has lone pair(s), which are attracted strongly to the hydrogen nucleus
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13
Q
  1. Van der Waals (VdW) Forces
    / Temporary Dipoles
A
  • A group of weak intermolecular forces that occur between molecules, which arise due to temporary / permanent dipoles in molecules
  • If you consider an atom to be a central positive nucleus surrounded by e- which are constantly in motion ,there will at any one time be at least one atom whose electrons are on one side or the other
  • This causes a temporary dipole within the atom itself
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14
Q

Order of strength of the intermolecular forces

A

H-bonds –> permanent dipole –> temporary dipole (Van der waals)

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15
Q

What affects the strength of the Van der Waals (VdW) Forces

A
  1. The strength of the Van der Waals forces increases with the number of e- in the atom / molecule, since the temporary dipoles can be of a larger size if there are more e-
    - –> (noble gases such as helium / neon, which exist as single atoms + have relatively few electrons, the forces are weak = explains their very low boiling point)
  2. The strength also depends on the shape of the molecule - long molecules can have induced temporary dipoles all along them
    - –> In general, larger molecules will have larger Van der Waals forces
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16
Q

Giant structures

What is diamonds structure?
(C)

A
  • Giant covalent structure
  • Each carbon atom is covalently bonded to 4 other carbon atoms
  • collectively, these 4 bonds create extremely strong intermolecular forces
  • Atoms arrang themselves in a tetrahedral shape
17
Q

Diamond’s physical properties

A
  • very high melting + boiling points
  • Insoluble in water + non-aqueous solvents
  • Solid at room temperature
  • Does not conduct electricity (all outer e- are held in localised bonds)
  • Good thermal conductor as vibrations travel easily through stiff lattice
  • Crystalline – the hardest known natural material
18
Q

Sodium chloride’s structure
NaCl

A
  • Giant ionic lattice
  • ‘giant’ as its made up of the same basic unit repeated over + over again
  • The Na+ and Cl- ions are packed together
  • lattice is cube shaped
19
Q

Sodium chloride’s physical properties

A
  • Solid at room temperature
  • High melting + boiling point
  • Soluble in water
  • Conducts electricity when molten / in solution
  • Crystalline
20
Q

Graphite’s structure
C

A
  • Giant covalent molecule
  • Arranged in layers held together by weak Van der Waals forces
  • The carbon atoms in the layers are arranged in hexagons (each connected to 3 others, the non-bonded e- from carbon joins with others.)
  • These delocalised e- flow along layers but
    not between them
21
Q

Graphite’s physical properties

A
  • Solid at room temperature
  • High MPt/BPt
  • Insoluble in water + non-aqueous solvents
  • Conducts electricity in one direction/plane only
  • Feels soft when rubbed (used as a lubricant) because pressure makes the layers move across each other as the weak bonding is broken
22
Q

Iron’s structure
Fe

A
  • Giant structure of cations surrounded by a ‘sea of
    delocalised electrons’
  • atoms in iron are held together by metallic bonds
23
Q

Iron’s physical properties

A
  • Solid at room temperature
  • High MPt/BPt
  • Conducts electricity in all directions
  • Insoluble in water and non-polar solvents
  • High density
24
Q

Iodine’s structure

A
  • Giant molecular structure
  • covalent bonds
  • Weak van der Waals forces hold the I2 molecules in a 3-dimensional structure
25
Iodine's physical properties
- Solid at room temperature - Low MPt/BPt (as molecules are attracted to each other only by Van der Waal intermolecular forces, that are weak) - Soft - Does not conduct electricity - Virtually insoluble in water, very soluble in non-polar solvents
26
Carbon dioxide's structure
- Simple molecular structure - strong covalent bonding within molecule, - but only weak van der Waals forces between the molecules - A small light molecule (RMM = 44)
27
Carbon dioxide's physical properties
- Gas at room temperature - Low MPt/BPt
28
# shapes of molecules What are lone pairs? Free radicals? What are bonding pairs?
- **Lone pairs** - 2 electrons that are not shared - on a dot+cross diagram, when there's 2 dots not shared for eg = lone pair - also called unshared e- / non-bonding pair - Free radicals = contain one unpaired e- = very reactive - **Bonding pairs** of e- are shared with another atom in a covalent bond
29
VESPR theory
FC = V - (N+B) FC- formal charge V- number of valence (e- on outer shell) N- number of non-bonding e- B- Number of Bonds calculations of this NOT coming up, but maybe just what the theroy is - **A model used to predict the shapes of molecules based on the idea that electron pairs around a central atom will arrange themselves to minimize repulsion**
30
What are charge clouds?
- Bonding pairs + lone pairs exist as charge clouds - A charge cloud is an area where u have a very big chance off finding an electron pair - The e- don't stay still in them - they whizz around inside the charge cloud
31
When drawing shapes of molecules, what does the thick wedge, and the broken line show? What's a tetrahedral shaped molecule look like
Thick wedge - bond coming out of page Broken line - bond going into page - Tetrahedral - has 4 e- pairs: Bond at top of central atom, and then bottom 3 bonds slightly closer together compared to top one (EG methane CH4) - If top bond replaced by lone pair = bottom 3 get closer together=smaller angles = Trigonal Pyramidal
32
Angles in molecule shape [VESPR theory]
- E- = negative charge = charge clouds will repel eachother as much as they can = e- pairs will orient themselves as far away as possible = predicts the geometry - **Lone-pair charge clouds repel more than bonding-pair charge clouds** - The greatest angle are between lone pairs of e- =bond angles between bonding pairs are reduced as they're pushed together by lone-pair repulsion - **Lone-pair/Lone-pair** angles are biggest --> **Lone-pair-bonding-pair** angles are 2nd biggest --> **Bonding-pair/Bonding-pair** angles are smallest
33
How would u work out the shape of a molecule + the number of lone + e- pairs
1. What's the central atom? [EG: O for H2O] 2. Use periodic table to see how many e- on its outer shell [O = 6] 3. Add the number of atoms that the central atom is bonded to to this number [H2O has 2: 6+2=8] (double bond would count as 2 not 1 eg CO2 has 2 =, so ud do 4 +4) 4. Divide this by 2 to find number of electron pairs on central atom [8/2 = 4 e- pairs] 5. Compare number of e- pairs to number of bonds to find number of lone pairs [H2O =2 bonding-pairs + 2 lone-pairs]
34
QS comin gup in exam
MCQ - Is the compoun polar / non-polar? [halide groups make compound polar] - What's the number of lone pair? - shape? - molarity? - RMM?
35
What is VSEPR + what does it predict?
VSEPR V - valence S - shell E - electron P - Pair R - Repulsion VSEPR predict the arrangment of e- pairs around a central atom
36
Steric effect Steric hindrance?
- When atoms occupy a space close to eachother, this costs energy + can change the shape + reactivity of molecules - Steric hindrance - slows chemical reactions due to presence of steric bulk
37
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