12.1 -12.2 Flashcards

1
Q

What are alkanes

A
  • saturated hydrocarbons
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2
Q

What does a compound being saturated mean

A
  • all the carbon bonds are bonded 4 times
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3
Q

What is the general formula of alkanes

A
  • CnH2n+2
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4
Q

What is the shape and bond angle of alkanes

A
  • tetrahedral (109.5)
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5
Q

Why do alkanes have a specific shape with specific angle

A
  • because the bond repel each other equally
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6
Q

If a molecule has no branching what does this mean

A
  • molecules can pack together closely leading to more surface contact
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7
Q

Why is the boiling point for longer straight chain high

A
  • they have more London forces so more energy is needed to overcome these forces so a high boiling point
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8
Q

What is the boiling point for branched hydrocarbons

A
  • they can’t pack closely together which weakens the London forces between the chain so they have a lower boiling point
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9
Q

What do alkanes form when they are completely combusted

A
  • CO2 and H2O
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10
Q

What are alkanes good as

A
  • fuels as most burn readily to produce large amounts of energy
  • used to power vehicles
  • used in most of Britain’s electricity
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11
Q

Using combustion equations:
15cm^3 of hydrocarbon ‘A’ burns completely in 120cm^3 of oxygen. 75cm^3 of carbon dioxide is produced what is the molecular formula of hydrocarbon A?

A

FORMULA: C5H12
1) use info to write a volume ratio equation
2) simplify ratio
3) 8 moles of O2 reacts to form 5 moles of CO2 and the ‘n’ moles of H2O. Any oxygen that isn’t in CO2 must be in H2O
4) combustion equation is
5) to identify ‘A’- all carbon in ‘A’ make CO2 and the number of hydrogens in ‘A’ must be 12 (we have 6H2O)

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12
Q

What is incomplete combustion

A
  • alkanes burning with a limited oxygen supply
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13
Q

What is produced in incomplete combustion

A
  • carbon monoxide(CO) and carbon(soot)
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14
Q

What problems does carbon monoxide cause

A
  • poisonous as it bonds to haemoglobin in the blood preventing oxygen from binding
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15
Q

What problems does soot cause

A
  • breathing problems
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16
Q

What reaction do alkanes undergo

A
  • free radical reactions
17
Q

What type of bond fission happens in free radical substitution reactions

A
  • homolytic fission
18
Q

What are the three steps of free radical substitution reactions

A

1) Initiation
2) Propagation
3) Termination

19
Q

What is the catalyst in free radical substitution

20
Q

What happens in initiation

A
  • radicals are produced by breaking a covalent bond forming two radical using UV light
21
Q

What happens in propagation

A
  • radicals react with non-radicals to form radicals and non radicals
22
Q

What happens in termination

A
  • 2 radicals react and form a non-radical molecules
  • ends the chain reaction
23
Q

Write the free radical substitution reaction for this reaction:
CH4 + Cl2 —> CH3Cl + HCl

A

Initiation:
UV
Cl2——> Cl . + Cl .

Propagation:
1) Cl . + CH4 —-> . CH3 + HCl
2) . CH3 + Cl2 —> CH3Cl + Cl .

Termination:
1) Cl . + Cl . —> Cl2
2) . CH3 + . CH3 —> C2H6
3) . CH3 + . Cl —> CH3Cl

24
Q

What are usually the products of free radical substitution reaction

A
  • normally a mixture of product
  • so it has a low percentage yield
25
Q

What is required to get your desired product in free radical substitution

A
  • further substitution