BS132 Lecture 4

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13 Terms

1
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What is Hybridisation Theory?

  • What might we expect from C?

  • What might it hybridise to form?

  • What happens to these hybrids?

  • Might expect C (2p2) to form CH2 instead of CH4

  • May hybridise 2s and 3 × 2p orbitals of C to give 4 degenerate sp3 orbitals

  • 4 sp3 electrons of C become paired upon forming sigma bonds w/ 4 H atoms

2
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What is the basis of Methane’s Shape?

2s non-directional, 3 × 2p orientated at 90 degrees

3
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What is the Mathematical Mixing of Methane?

4 x sp3 orbitals at 109.5 degrees

4
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What is Methane’s Shape?

Tetrahedral

5
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What makes Methane energetically favourable?

Minimum repulsion between bonding electron pairs

6
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What type of bonds are in the C=C Double Bond?

1 sigma and 1 pi

7
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What happens to each C atom in the C=C Double Bond?

Sp2 hybridised so has 1 unhybridised p orbital

8
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How are the sp orbitals in Ethane different to Ethene?

Tetrahedral around each sp3 hybridised atom

9
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What happens to the unhybridised p orbitals in ethene?

Unhybridised p orbtials in ethene are orientated so they overlap to form a pi bond

10
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How does the rigidity of Ethane compare to Ethene?

Isn’t as rigid, rotation around C=C isn’t possible due to pi bond

11
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How does the strength of Alkenes compare to Alkanes?

C=C is stronger and shorter than C-C

12
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What type of bonds are in C-C?

Sigma

13
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What type of bonds are in C=C?

Pi and Sigma