Alkenes and their Bonding Flashcards

1
Q

what is the difference between alkenes and alkanes

A
  • alkanes only have single bonds between their carbon atoms

- whereas alkenes have at least one double bond between a pair of carbon atoms

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2
Q

what does it make alkenes if they have at least one C=C bond

A

unsaturated

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3
Q

between alkanes and alkenes which one is more common

A

alkanes

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4
Q

how do you get alkenes

A
  • they dont naturally occur in nature

- so they have to be made through cracking alkanes

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5
Q

what would the structural formula for ethene be

A

CH2=CH2

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6
Q

what would the structural formula for propene be

A

CH2=CH-CH3

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7
Q

what would the structural formula of cis-but-2-ene be (just explain)

A
  • there would be a C=C bond in the middle
  • with a CH3 coming from the left and right carbon atom
  • both at opposite sides from each other (Z-isomer)
  • two Hs would be bonded to a C each as well
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8
Q

what is the general formula of an alkene

A

CnH2n

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9
Q

what is a common cyclic alkene and what is its structural formula

A
  • cyclohexene
  • CH=C(H)-C(H2)-C(H2)-C(H2)-C(H2)-back to the first CH
  • the hydrogens are in brackets as to show that it is the carbon atoms that are bonded together to make the ring
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10
Q

what is an advantage that alkenes have over alkanes due to their C=C bond

A
  • they are more reactive than alkanes

- so they can be used in many more useful reactions

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11
Q

why does using the C=C symbol seem to be misleading about how the carbon atoms are bonded

A
  • because it implies that the two bonds between the carbon atoms are the same
  • when they are not
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12
Q

how many atoms are the carbon atoms in a C=C bond bonded to

A
  • 2 other atoms
  • as two bonds are being used to bond with another carbon atoms
  • where it would normally have 4
  • as carbon has 4 electrons in its outer shell
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13
Q

what does covelant bonding between atoms usually involve

A
  • the overlapping of the orbitals of two different atoms

- these could be 2 s orbitals, 2 p orbitals or one of each

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14
Q

what are all these bonds represented by when drawn and what is the example when drawing hydrogen gas

A
  • a line

- so hydrogen gas, H2, would be drawn as H-H

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15
Q

what can all of these simpler covelant bonds be called

A
  • sigma bonds

- also known as o (with a line on top) bonds

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16
Q

when sigma bonds are formed between carbon atoms in an alkene, what is their formation called

A
  • formation by axial overlap

- or end-on overlap

17
Q

in a molecule of ethene, how many sigma bonds would each carbon atoms have

A
  • 3

- because they are bonded with one carbon atom and 2 hydrogens each

18
Q

what does that mean regarding the electrons in carbons outer shell

A
  • the two carbon atoms each have one electron in a p orbital left
  • which hasnt been used in bond formation
19
Q

what is the relationship between the p orbitals in this molecule of ethene and what does it mean

A
  • they are parallel to each other
  • and so are not able to overlap with each other
  • in the same way as in the formation of sigma bonds
20
Q

however, what happens when the p orbitals do overlap

A

it results in the formation of two regions of negative charge above the C-C sigma bond

21
Q

how would this bond between p orbitals form in the first place

A

it is formed by the sideways overlap of orbitals

22
Q

what are these types of bonds called

A
  • pi bonds

- also known as (literally the sign for pi) bonds

23
Q

if each of these regions of negative charge contain one electron, what is made

A
  • they make up a second pair of electrons
  • between the carbon atoms
  • as one region of negative charge is above the C-C sigma bond and the other is under
24
Q

what is different about the electrons in the pi bond compared to the sigma bond

A

they are further away from the carbon atoms than the electrons in the sigma bonds are

25
Q

what does it mean if the electrons in the pi bond are further away from the carbon atoms

A
  • they can be though of as less under control by the carbon atoms
  • and therefore more available for reactions
  • this is why they are more reactive than alkanes