Week 1 Lectures Flashcards

1
Q

Define elements

A

A substance that cannot be broken down to other substances by chemical reactions

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2
Q

How many naturally-occurring elements are there?

A

92

Each one has a unique symbol, usually from the first one or two letters of the name, often from Latin or German

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3
Q

Systems become as stable as possible to…

A
  • minimise their energy and maximise their entropy
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4
Q

How many elements are known to be essential for life?

A

About 25!

Four elements: carbon, oxygen, hydrogen, nitrogen - make up 96% of living matter

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5
Q

Define atom

A

Smallest unit of matter which still retains the properties of an element

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6
Q

Mass of proton and neutron =

A

1.66 x 10^-24 g

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7
Q

What is atomic number

A

Number of protons

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8
Q

Atomic mass

A

Sun of masses of all components (e, p, n)

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9
Q

An isotope…

A

Different mass number, same atomic number

They all have exactly the same chemical properties ! (Chemically identical but different masses)

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10
Q

Name 3 different types of atomic orbitals

A

1s —> 2 electrons
2s —> 2 electrons
2P —> 6 electrons (total - 2 in each)

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11
Q

What is a compound?

A

A substance consisting of two or more elements on a fixed ratio

For example, table salt (NaCl) is a compound with equal numbers of chlorine and sodium atoms.

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12
Q

List 4 different bonds

A

Covalent

Hydrogen

Ionic

van der Waal’s

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13
Q

What is a covalent bond

What is the different between non-polar and polar

A

Sharing of electrons by two atoms

Polar covalent bonds are not equal sharing, while non-polar covalent bonds are equal sharing

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14
Q

Hydrogen bonds form…

A

Molecules with polar bonds!

  • they’re weak compared with covalent or ionic bonds. But are very strong when together
  • they’re crucial to life on earth!
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15
Q

Ionic bonds form when

A

Form when two atoms, very different in attraction for valence electrons come together.

A crystal is formed. (Between ions)

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16
Q

van der Waal’s forces

A

Form between molecular substances such as non-polar and polar. Once formed, electrons tend to be stable!

  • they’re very weak
  • Strength = 0.5kJ/mole
  • very short range
  • collectively strong
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17
Q

Formation of water molecule

A

Polar covalent bonds

Nucleus has slightly (delta) negative charge, so H has slightly positive charge

2 low e- pairs, where negative charge sits, not involved in bonding

2 e- shared with H, involved in bonding

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18
Q

What is an orbital level?

A

A region of space an electron inhabits around the nucleus of an atom

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19
Q

What is the code for a hybrid orbital?

A

SP^3
(3P orbital and 1S orbital together)

Where different orbital levels mix due to different energy levels

20
Q

Orbital shapes of the different level orbitals

A

S = Spherical shape around the nucleus
P = Dungbell shape
Hybrid = Balloon shape (combination of S and P)

21
Q

Electronegativity is?

A

The tendency of an atom to attract emectrons

22
Q

Water molecule shape?

A

Each bond is directed towards one corner of a tetrahedron (usually angle of 109.5°)

(Not shared electrons held closer to nucleus by O2)
Long pairs repel each other more than bonding pairs, reducing bond angle to 104.5°

2 lone pairs bond to the other H2O due to delta negative / positive attracting each other, and join via a hydrogen bond!

23
Q

Effect of hydrogen bonds in water: 1

A

Higher boiling point

Have to use energy to break collectively strong H bonds before vapour can be made

24
Q

Effect of hydrogen bonds in water: 2

A

Higher cohesion

Allows a whole column of water to travel up the xylem and into the leaf during transpiration
(Cohesion tension theory)

25
Effect of hydrogen bonds in water: 3
High heat of vaporisation (Energy to convert 1G of water from liquid to gas at 25°) 580 calories (2426.72J) to convert 1G of water to a gas - meaning sweat cools us down as kinetic energy of water molecule left is reduced, so a cooling action occurs as energy is reduced/lost
26
Effect of hydrogen bonds in water: 4
Ice floats Has a crystallised latis structure, (more open structure than water) so is less dense as bonds are held slightly further apart. Therefore in low temperature, ice floats so aquatic organisms can remain under the body of water… under the insulating layer!
27
Effect of hydrogen bonds in water: 5
Higher surface tension Vamiscuous layer (dips in the middle, acts like skin) so insects and plant life can live a top of the surface!
28
Effect of hydrogen bonds in water: 6
Higher specific heat capacity (Amount of heat absorbed or lost in order to alter the temperature of 1G of water by 1°) - water resists changing its temperature. Lots of energy is required to heat and cool hydrogen bonds to break or reform them! This bumps water temperature and allows a long time to cool/heat, which is an advantage for aquatic life!
29
Effect of hydrogen bonds in water: 7
Water is a good solvent for polar molecules! Interact/react with any polar molecules such as alcohol! This is because O2 is electronegative, so it can interact with its lone pairs and bond to a positive bond
30
Effect of hydrogen bonds in water: 8
Water is a good solvent for ionic compounds eg NaCl Anything that carries positive or negative charge can interact and be dissolved by a hydration shell!
31
Hydration shell
A hydration shell is a structured arrangement of water molecules that surround an ion or a polar molecule when it dissolves in water based on its charge. If negative charge, water will angle towards it slightly positive If positive charge, water will angle towards it slightly negative
32
Effect of hydrogen bonds in water: 9
Oil drop effect Water molecules next to the hydrophobic (non-polar) molecules cannot satisfy their H-bonding requirements so are less stable. To maximise number of H bonds which can be formed, clustering of non-polar molecules occurs!
33
Why oil drop effect on water?
Can shake and it will mix for short period of time, but after long period of time it will separate! This is because it doesn’t like to be mixed with hydrophobic/non-polar molecules due to H bonds wanting to be as stable as possible so we end up with a cluster of non-polar molecules Did you know: This is why amino acids arrange themselves in such a way where hydrophobic region faces inwards and hydrophilic region faces outwards!
34
Molecular mass =
Sum of masses of all atoms in a molecule (daltons)
35
1 molecule of a compound always contains Avogadro’s number. What is this number?
6.02 x 10^23 molecules
36
Anything in what symbol means concentration?
[ ] Square brackets
37
What is pH?
A measure of ‘acidity’ (Or the concentration of protons (H+) present in an aqueous solution)
38
What is the pH scale called?
Logarithmic scale from 1 to 14 1 extremely acidic (high [H+]) 14 extremely basic (low [H+])
39
Features of Carbon compounds? (Organic chemistry)
Carbon has unique ability to form chains which are stable to air and water C bonds to 4 atoms (1s^2, 2s^2, 2p^2 - it needs to share 4 electrons from elsewhere) It’s tetravalent Nearly all molecules cells use to function are carbon based (DNA, protein, carbohydrate)
40
pH equation
pH = -log([H+]) So, [H+] = 10^-pH
41
Water dissociation constant (Pure water)
Kw = [H+] [OH-] = 10^-14
42
How many atoms does C bond to?
4 It’s Tetravalent (Each carbon is tetrahedral if all carbons single-bonded)
43
List functional groups of molecules involved in chemical reactions
Hydroxyl - form H bonds by donation or acceptance of H+ Amino - Sulphhydryl - disulphide bridge covalently links two cysteines Carbonyl - are reactive Carboxyl - important for protein formation; can donate proton into environment and will carry a negative charge Phosphate - formation of ATP or phosphate backbone
44
What are isomers
Two organic molecules with the same number of atoms of the same elements but different structures
45
Different types of isomerism
- structural: differ in covalent partners - geometric: differ in arrangement around a double bond - enantiomers: have identical physical and chemical properties (therefore very difficult to separate)
46
What is an enantiomer
Molecules which differ only in spatial arrangement of groups around a central ‘asymmetric’ carbon atom They differ in the way they interact with other optically active compounds (They’re mirror images of one another - cannot be superimposed upon one another)