Fundamentals of chemistry Flashcards

(41 cards)

1
Q

Cathode ray tube

A

Cathode is negativley charged
Anode is positivley charged
electron flow from the cathode and are attracted to the anode
small holes in the anode create a beam of electrons - so electrons can behave as a wave

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2
Q

Heisenberg uncertainty principle

A

It not possible to know both the position and velocity of an electron at the same time

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3
Q

How can we prove that electrons act as a wave

A

If you have an electron moving along, and you put an object in the way with a small hole in it you will get curvatures behind the object. This is known as a DIFFRACTION pattern ( a property of waves) If you put an object with 2 holes in it you will also see a diffraction around both holes causing an interference pattern. If it were acting as a particle it would only be able to go through one hole.

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4
Q

Hydrogen atomic orbitals - quantum numbers

A

n - energy levels - 1–
L - Assymetry of orbitals (0 - (n-1) )
m1 - degenracy of orbitals (-l - +l)
ms - electron spin (positive or negative)

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5
Q

Pauli exclusion principle

A

No two electrons in an atom can have the same 4 quantum numbers, each orbital can accommodate two electrons one of each spin (ms)

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6
Q

atomic orbital

A

orbital around one element

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7
Q

Molecular orbital/bonding orbital

A

Orbital around a molecule eg 2 H atoms

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8
Q

Orbitals in phase (Example Hydrogen)

A

also knowns as constructive interferance
leads to a bigger wave and forms a bond between the two hydrogen atoms leading to a bonding orbital. this is lower bonding than the anti-bonding orbital.

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9
Q

Orbitals out of phase (example Hydrogen)

A

Leads to destructive interference which leads to a flat line. So there is no orbital between the two hydrogen atom (ie no bond ) this is called an anti bonding orbital. this is higher energy than the bonding orbital.

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10
Q

What happens if another electron is added to H2

A

the electron is added to the anti-bonding orbital

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11
Q

Bond order equation

A

Bond order = 1/2(number of electrons in bonding orbital - number of electrons in antibonding orbital)
a positive bond order indicates a stable bond and a bond order of zero indicates the molecule is unstable

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11
Q

Molecular orbital theory

A

Bonding orbitals - Electrons in bonding orbitals stabilize the molecule
Anti bonding orbitals - Electrons destabilize the molecule as they are found on the outside region not between the nuclei

Molecular orbitals -

σ orbitals - formed by head on overlap ( 2s/2p)
𝜋 orbitals - formed by side on overlap of p orbitals (2p)
σ* - antibonding orbitals

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12
Q

σ bond

A
  • lower energy ie. more table
  • 1st bond between 2 (C,N,O) atom is always a σ bond
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13
Q

𝜋 bond

A

2nd/3rd bond between 2 atoms is always a 𝜋 bond
Will always be first bond to break

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14
Q

Hybrid orbital

A

1st bond between 2 (C,N,O) atoms always involves a hybrid orbital

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15
Q

p orbital

A

2nd/3rd bond between 2 atoms always involves a p orbital

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16
Q

How long is a single bond

A

1.5 A
1A = 1x10^-10 m

17
Q

How long is a double bond

18
Q

How to identify sigma and pi bonds

A

single bond - Always 1 sigma bond
Double bond - 1 sigma + 1 pi bond
Triple bonds - 1 sigma + 2 pi bonds

19
Q

Resonance stabilisaton

A

Happens when electrons are delocalised in a ring structure so they move around the whole structure, so the structure can be presented in multiple ways. Eg in C4H4O the oxygen can become positively charged as the electrons move around.
IMPORTANT
When moving electrons in resonance connectivity(skeletal structure) cant change
only lone pairs and pi bonds can be moved

20
Q

What determines hybridisation

21
Q

sp2 - shape

A

trigonal - 120 degrees

22
Q

sp3 shape

A

tetrahedral - 109 degrees

23
Q

sp shape

A

linear - 180 degrees

24
Partial bond meaning
it cant be rotated
25
What bonds are strong sigma or pi bond
sigma
26
Structural isomerism
same formula, different connectivity
27
stereoisomers
Molecules with the same connectivities but different 3D shape
28
Enantiomers
a molecule with a chiral centre and its mirror equivalent
29
nomenclature of enantiomers
1. Priority of the atoms according to atomic number 2. if moving in a clockwise direction - R if moving in a anticlockwise direction - S
30
How to seperate enantiomers
- retention of chiral centre - In solution enantiomers will take part in the same chemical reactions at same rate but if other molecule has a chiral centre the reaction rates and products can be different. This is important for enzymes as they have chiral centres so will react with one enantiomer but not the other
31
dihedral angle
rotation around c-c bonds (angle between 2 planes)
32
a plane
3 molecules make up a plane
33
types of conformation
A) staggered - most stable (lowest energy) b) gauche c) eclipsed d) fully eclipsed - least stable (highest energy)
34
Why is the staggered conformation more stable ?
Because in the eclipsed conformation have methyl groups closer together. This means the the electrons in the atomic orbitals repel each other so atoms that are not directly bonded cannot be too close.
35
different conformations for cyclic molecules
Boat - less stable chair - more stable
36
Different positions in a trigonal bypyramidal shape
Equatorial - atoms around the equator (preferred as less electron repulsion) Axial - atoms straight up and down
37
Newman projection
loking down c-c bond
38
fischer projection
used for sugars
39
Howarth projection
rign and sugars in cyclic form
40