U3-1 - Molecular Orbitals Flashcards

1
Q

How can you tell the number of carbons in this structure?

A

Count each ‘kink’ on the zigzag, including the ends.

This structure has 7 carbons.

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2
Q

How can you tell how many hydrogens are atached to the circled carbon?

A

No. of H = 4 – No. of bonds made

This carbon makes 3 bonds, so must have 1 H.

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3
Q

Two atomic orbitals combine to make ___ molecular orbitals.

A

two

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4
Q

What is the difference between bonding and antibonding orbitals?

A

Antibonding orbitals are higher in energy.

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5
Q

How do sigma bonds form?

A

End on overlap of atomic orbitals

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6
Q

How do pi bonds form?

A

Side on overlap of atomic orbitals.

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7
Q

Which bonds are stronger, sigma or pi?

A

Sigma (better overlap of atomic orbitals)

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8
Q

How do you count the number of sigma and pi bonds in a molecule?

A

Single bonds are always sigma.

In double and and triple bonds, first bond is sigma, the rest are pi.

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9
Q

Type of hybridisation found in alkanes

A

sp3

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10
Q

Type of hybridisation found in alkenes and aromatic rings

A

sp2

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11
Q

Type of hybridisation found in alkynes (C≡C)

A

sp

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12
Q

Bond angle associated with sp3 hybridisation

A

109.5 (tetrahedral)

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13
Q

Bond angle associated with sp2 hybridisation

A

120 (trigonal planar)

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14
Q

Bond angle associated with sp hybridisation

A

180 (linear)

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15
Q

Explain how sp3 hybrid orbitals form

A

One s and three p orbitals mix to form four degenerate sp3 atomic orbitals

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16
Q

Explain how sp2 hybrid orbitals form

A

One s and two p orbitals mix to form three degenerate sp2 atomic orbitals

17
Q

Explain how sp hybrid orbitals form

A

One s and one p orbital mix to form two degenerate sp atomic orbitals

18
Q

Which orbitals overlap to form sigma bonds in alkanes?

A

sp3 hybrid orbitals (overlap end on)

19
Q

Which orbitals overlap to form pi bonds in alkenes and aromatic rings?

A

unhybridised 2p orbitals (overlap side on)

20
Q

Which orbitals overlap to form sigma bonds in aromatic rings?

A

sp2 hybrid orbitals (overlap end on)

21
Q

Formula for benzene

A

C6H6

22
Q

Benzene structure (skeletal)

A
23
Q

Benzene structure (full)

A
24
Q

State the feature that provides stability to aromatic rings.

A

Delocalised electrons

25
Q

Explain what is meant by the highest occupied molecular orbital (HOMO).

A

Highest bonding molecular orbital containing e.

26
Q

Explain what is meant by the lowest unoccupied molecular orbital (LUMO).

A

Lowest antibonding molecular orbital (no e present)

27
Q

An organic complex is colourless if it absorbs ______ light.

A

UV

28
Q

An organic complex absorbs UV light. Why is this?

A

Large energy gap between HOMO and LUMO

29
Q

Chromophore

A

A group of atoms within a molecule that is responsible for absorption of light in the visible region of the spectrum.

30
Q

State what happens to e when a chromophore absorbs light

A

An e is promoted from HOMO to LUMO

31
Q

Chromophores exist in molecules containing a _______________ _________.

A

conjugated system

32
Q

Conjugated system

A

A system of adjacent unhybridised p orbitals that overlap side-on to form a molecular orbital across a number of C atoms.

33
Q

What structural feature is present in conjugated systems?

A

Alternating single and double bonds

34
Q

A system of adjacent unhybridised p orbitals that overlap side-on to form a molecular orbital across a number of C atoms.

A

Conjugated system

35
Q

Electrons in a conjugated system can be described as __________.

A

delocalised

36
Q

How can you compare the sizes of conjugated systems in different molecules?

A

Count the no. of (alternating) double bonds. More double bonds = larger conjugated system.

37
Q

The more atoms in the conjugated system, the ___________ the energy gap between HOMO and LUMO.

A

smaller

38
Q

The larger the conjugated system, the _________ the wavelength of light absorbed.

A

longer (lower E)

39
Q

When the wavelength of light absorbed is in the visible region, the compound will exhibit the __________________ colour.

A

complementary