Organic Chemistry - 3)a) Molecular Orbitals Flashcards

2)a) Molecular Orbitals (27 cards)

1
Q

where do electrons of different spin spend most of their time between the two nuclei?

A

the bonding orbital

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2
Q

what is the bonding orbital?

A

where it is most likely to find electrons

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3
Q

what determines the shape of a molecular orbital?

A

quantum mechanics

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4
Q

why are antibonding orbitals formed?

A

the number of combining atomic orbitals is the same as the number of molecular orbitals formed, so bonding and antibonding orbitals are formed

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5
Q

state three properties of antibonding orbitals:

A

they have higher energy than bonding and atomic orbitals

they are a different shape

they do not contain electrons

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6
Q

what type of bonding arises as a result of end-on-end overlapping of atomic orbitals?

A

sigma bonds

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7
Q

how are Pi bonds formed?

A

by the side-on-side overlap of p-orbitals

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8
Q

when do Pi bonds occur?

A

when atoms form multiple bonds
(c=c)

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9
Q

what is weaker out of the Pi and Sigma bonds?

A

Pi bonds

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10
Q

what is sp3 hybridisation?

A

the mixing of one s orbital and three p orbitals to form four sp3 hybrid molecules of equal energy

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11
Q

what is sp2 hybridisation?

A

the mixing of one s and two p orbitals to form three sp2 orbitals of equal energy, leaving on p orbital unchanged

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12
Q

how are pi bonds formed?

A

the unhybridised p orbitals overlap side-on-side to form a pi bond

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13
Q

why are sigma bonds stronger than pi bonds?

A

they are very efficient at overlapping

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14
Q

why are pi bonds weaker?

A

they are formed by the side-on-side overlapping of unhybridised p orbitals which is less efficient and hence form weaker bonds

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15
Q

what is sp hybridisation?

A

the mixing of one s and one p orbital, leaving two unhybridised p orbitals

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16
Q

alkynes contain a carbon to carbon triple bond, describe in detail, the hybridisation and bonding that occurs in a triple bond:

A

one s and one p orbital mixes to form two sp orbitals. The sp orbitals overlap end-on-end to form a sigma bond. The two unhybridised p orbitals over lap side-on-side to form two pi bonds.

17
Q

what type of hybridisation is present in alkanes?

A

sp3 hybridisation

18
Q

what type of hybridisation is present in alkenes?

A

sp2 hybridisation

19
Q

what type of hybridisation is present in alkynes?

A

sp hybridisation

20
Q

what type of compounds appear colourless?

A

saturated (sigma bonds only)

21
Q

why do saturated compounds appear colourless?

A

they only contain sigma bonds. The HOMO is the sigma bonding orbital and LUMO is the sigma antibonding orbital. This energy gap is very large and hence corresponds to the ultraviolet part of the spectrum. No visible light is absorbed and so the compound is colourless.

22
Q

what can be said about unsaturated compounds like ethene or butene?

A

they contain simple pi bonds and hence still have a large transition to promote electrons from HOMO to LUMO. They also absorb light from ultraviolet part of the spectrum and appear colourless

23
Q

what happens when light is absorbed?

A

the energy from photons is used to promote excited electrons from the HOMO to LUMO

24
Q

what structures do coloured compounds contain?

A

conjugated system

25
what is a conjugated system?
a long chain of alternating double and single bonds
26
summarise how a conjugated system works:
the alternating sigma and pi bonds in a benzene ring allows the electrons to become delocalised. The molecular orbitals containing the delocalised electrons stretch along the length of the conjugated system. The larger the conjugated system, the smaller the energy difference between the HOMO and LUMO. This means that the excited electrons will require less energy
27
what is a chromophore?
the group of atoms within a molecule that is responsible its colour