S2 Chemistry HL

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Last updated 1:02 PM on 1/11/26
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36 Terms

1
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Define Ionic bonding

Electrostatic attraction between oppositely charged ions

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Define Covalent bonding

Electrostatic attraction between a shared pair and positively charged nuclei.

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Define Metallic bonding

Electrostatic attraction between a lattice of cations and a sea of delocalised electrons

4
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Properties of Ionic bonding

High melting points, low volatility, generally high solubility (in polar compounds), high conductivity (when molten), high brittleness

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Properties of Covalent bonding

Low melting point, high volatility, low solubility, poor conductivity, high brittleness

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Properties of Metallic bonding

High melting points, low volatility, very low solubility, high conductivity, high malleability and ductility.

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Volatility

A substance’s tendency to vaporise

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Solubility

The ability of a substance to dissolve another substance to form a uniform mixture/solution

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Conductivity

The ability of charged particles to move through a region of space

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Brittleness

a material's tendency to fracture or shatter suddenly under stress with little to no plastic (permanent) deformation.

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Malleability

Ability to be bent/reshaped when compressed

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Ductility

Ability to be drawn out into wire when stretched

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Bond polarity

Results from the difference electronegativities

<p>Results from the difference electronegativities </p>
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Polarity

Related to the way electrons are distributed within molecules/bonds

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Molecular polarity

describes electron distribution throughout whole molecules

<p>describes electron distribution throughout whole molecules </p>
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Polar molecules

When the electron distribution leads to a partial negative charge on one end of the molecule and a partial positive on the other. Creating a dipole moment, (In other words they look asymmetrical)

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Intermolecular forces

Electrostatic forces of attraction that keep molecules together

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London dispersion forces

Temporary induced dipole via random electron movement.

Occur in all molecules

<p>Temporary induced dipole via random electron movement. </p><p>Occur in all molecules </p>
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LDF Examples

He, Ne, Ar, Kr, O2, N2, I2, Cl2, CH4, C2H6, CO2

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Dipole induced dipole

The presence of a permanent dipole in the polar molecule induced the formation of temporary dipole in the neighbouring non-polar molecule

Between polar and non-polar molecules

<p>The presence of a permanent dipole in the polar molecule induced the formation of temporary dipole in the neighbouring non-polar molecule </p><p>Between polar and non-polar molecules </p>
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Dipole Induced Dipole examples

O2, I2, HCL, Ar

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Dipole Dipole

When a molecule is polar, it has a permanent dipole, therefore experiences dipole-dipole forces of attraction with neighbouring polar molecules

Between polar molecules ONLY

<p>When a molecule is polar, it has a permanent dipole, therefore experiences dipole-dipole forces of attraction with neighbouring polar molecules </p><p>Between polar molecules ONLY </p>
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Hydrogen bonding

Intermolecular attraction between two molecules which contain a hydrogen bond to a highly negative element like F,O,N

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Van Der Waal Forces

LDF/Dipole-Dipole/Dipole-induced Dipole

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Order of IMF (weakest-strongest)

LDF → D-ID→ D-D→ H bonds → Ionic/Covalent

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Covalent network structures

Vast/continuous 3D structures linked via strong covalent bonds/extreme hardness/high melting points

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Allotropes + arrangement

Diamond (tetrahedral) / Graphite (C atom bonded to 3 other c atoms) / Graphene (one layer of graphite

<p>Diamond (tetrahedral) / Graphite (C atom bonded to 3 other c atoms) / Graphene (one layer of graphite </p>
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Resonance bonds AHL

Two or more possible resonance structures to represent a molecule

<p>Two or more possible resonance structures to represent a molecule </p>
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Hybridisation AHL

Concept of mixing atomic orbitals to form new hybrid orbitals of new shapes

<p>Concept of mixing atomic orbitals to form new hybrid orbitals of new shapes </p>
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Electron geometry

determined by the total number of electron domains (both bonded pairs and lone pairs) surrounding a central atom

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Molecular Geometry

Describes the arrangement of only the atoms, ignoring lone pairs, resulting in the molecule's actual 3D shape

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<p><span>EG:Linear (2)</span></p>

EG:Linear (2)

2 pairs
No lone pairs = Linear
1 lone pair = Linear

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<p><span>EG: Trigonal Planar (3)</span></p>

EG: Trigonal Planar (3)


3 e groups
0 lone pairs = Trigonal Planar
1 lone pairs = Angular

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<p><span>EG: Tetrahedral (4)</span></p>

EG: Tetrahedral (4)

4 be- groups

0 lone pairs

BA: 109.5

MG: Tetrahedral
OR

3 be-groups

1 lone pair

<109.5

MG: trigonal pyramidal


OR

2 be- groups

2 lone pairs

«109.5

MG: bent

<p>4 be- groups </p><p>0 lone pairs </p><p>BA: 109.5 </p><p>MG: Tetrahedral <br>OR </p><p></p><p>3 be-groups </p><p>1 lone pair </p><p>&lt;109.5 </p><p>MG: trigonal pyramidal  </p><p><br>OR </p><p>2 be- groups </p><p>2 lone pairs </p><p>«109.5 </p><p>MG: bent <br></p>
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EG: Trigonal bipyramidal (5)

5 be- groups

0 lone pairs

BA: 120 (équatorial)/ 90 (axial)

MG: Trigonal bipyramidal

OR

4 be- groups

1 lone pairs

BA: <120 (équatorial)/ <90 (axial)

MG: Seesaw

OR

3 be- groups

2 lone paris

BA: <90

MG: T shaped

Or

2 be- groups

3 lone pairs

BA: 190

MG: Linear

<p>5 be- groups </p><p>0 lone pairs </p><p>BA: 120 (équatorial)/ 90 (axial)</p><p>MG: Trigonal bipyramidal</p><p>OR </p><p>4 be- groups </p><p>1 lone pairs </p><p>BA: &lt;120 (équatorial)/ &lt;90 (axial)</p><p>MG: Seesaw </p><p>OR </p><p>3 be- groups </p><p>2 lone paris </p><p>BA: &lt;90 </p><p>MG: T shaped </p><p>Or </p><p>2 be- groups </p><p>3 lone pairs </p><p>BA: 190 </p><p>MG: Linear </p>
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EG: Octahedral (6)

6 Be- groups

0 Lone pairs

BA: 90

MG: Octahedral

OR
5 Be- groups

1 lone pair

BA: <90

MG: square pyramidal

OR

4 Be- groups

2 lone pairs

BA: 90

MG: square planar

<p>6 Be- groups </p><p>0 Lone pairs</p><p>BA: 90</p><p>MG: Octahedral </p><p>OR <br>5 Be- groups </p><p>1 lone pair </p><p>BA: &lt;90 </p><p>MG: square pyramidal</p><p>OR</p><p>4 Be- groups </p><p>2 lone pairs</p><p>BA: 90 </p><p>MG: square planar </p>