Organic Chemistry 4.1-4.28 Flashcards

1
Q

4.1 What is a hydrocarbon?

A

A compound of hydrogen and carbon only

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2
Q

4.2 How do you represent molecules using molecular formulae

A

Actual number of each type of atom present e.g. C2H4 = ethene

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3
Q

4.2 How do you represent molecules using empirical formulae?

A

Simplest whole number ratio e.g. C2H6 = CH3

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4
Q

4.2 How do you represent molecules using general formulae

A

General formula for the homologous series e.g. CnH2n

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5
Q

4.7 What is crude oil

A

A mixture of hydrocarbons

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6
Q

4.2 How do you represent molecules using a) structural formulae b) displayed formulae

A

a) How the atoms are joined together

b) Show all bonds in the molecule as lines (covalent bond)

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7
Q

4.3 What is a homologous series?

A

Group of compounds with
- same general formula, trends in their physical properties, similar chemical properties, trends in their physical properties, each successive member differs by CH2, same functional group

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8
Q

4.3 What is a functional group

A

An atom or group of atoms that determines the chemical properties of the compound

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9
Q

4.20 What does saturated mean

A

Contains single bonds only

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10
Q

4.19 What is the general formula of alkanes

A

CnH2n+2

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11
Q
  1. 4 What is the number of carbon atom(s) in
    a) propane
    b) ethane
    c) methane
    d) butane
A

3, 2, 1, 4

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12
Q

4.6 Reaction of alkanes with bromine with ultraviolet light

A

A substitution reaction occurs as a hydrogen atom on the alkane has been replaced by a bromine atom

methane + bromine (red/brown) -> bromomethane + hydrogen bromide (colourless)
CH4 + Br2 -> CH3Br + HBr

More examples:
C3H8 + Br2 -> C3H7Br (Bromopropane) + HBr

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13
Q

4.6 Combustion of alkanes

A

Complete combustion: alkane + oxygen -> carbon dioxide + water
e.g. CH4 + 2O2 -> CO2 +2H20

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14
Q

4.6 and 4.12 Combustion of alkanes continued

A

Incomplete combustion occurs with an insufficient supply of oxygen
alkane + oxygen -> carbon monoxide + water
alkane + oxygen -> carbon + water

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15
Q

4.3 What is structural isomerism

A

Structural isomers are molecules with the same molecular formula, but different structural formulae

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16
Q

4.8 How does fractional distillation separate crude oil into fractions

A
  1. Crude oil is heated and enters the fractioning column
  2. The column is hotter at the bottom and gets cooler as you go up
  3. Large molecules with high boiling points condense near the bottom
  4. Small molecules with low boiling points remain as gases and leave at the tap
17
Q

4.9 What are the uses and names of the main fractions obtained from crude oil (6)

A

a) Refinery gases - liquefied petroleum gas for domestic cooking
b) Gasoline - fuel in cars
c) Kerosene - fuel for jet aircrafts, domestic heating oil and ‘paraffin’ for small heaters and lamps
d) Diesel- fuel for buses and lorries
e) Fuel oil - fuel for ships
f) Bitumen - road surface tar

18
Q

4.13 Why is carbon monoxide poisonous

A

Carbon monoxide is toxic because it reduces the capacity of blood to transport oxygen around the body

19
Q

4.11 What is a fuel

A

A substance that when burned releases heat energy

20
Q

4.10 What are the trends in the main fractions of a) colour b) boiling point and c) viscosity

A

Molecules get larger as you go down
Colour lighter at top and darker at the bottom
Boiling point lower at the top and higher at the bottom
Viscosity lower at the top (runny) and higher at the bottom (thicker)

21
Q

4.14 Why in car engines can nitrogen and oxygen react

A

The temperature reached is high enough to allow nitrogen and oxygen from air to react, forming oxides of nitrogen

N2 (g) + O2 (g) ->2NO (g) nitrogen oxide
N2 (g) + 2O2 (g) -> 2NO2 (g) nitrogen dioxide

22
Q

4.15 How does sulphur dioxide form via combustion

A

Fossil fuels contain sulfur as an impurity and when they burn, the sulfur is also oxidised to form:

sulfur dioxide = S(s) + O2 (g) -> SO2 (g)

and in water forms an acidic solution sulfurous acid =
SO2 (g) + H20 (l) -> H2SO3 (aq)

+ oxygen = 2H2SO3 + O2 -> 2H2SO4 (sulfuric acid)

23
Q

4.16 How does sulfur dioxide and oxides of nitrogen contribute to acid rain

A

They dissolve in water to form acidic solutions

24
Q

4.18 Why is cracking necessary

A

The supply of short chain hydrocarbons from crude oil is not enough to meet demand

Supply of long chain hydrocarbons is larger than demand

25
Q

4.17 How are long chain alkanes converted by cracking

A

Long chain alkanes are converted to alkenes and shorter-chain alkanes by catalytic cracking

By heating fuel oil until it is a gas, then passing it over a catalyst, made of silica or alumina at a temperature in the range 600-700C

Thermal decomposition

26
Q

4.21 How can you work out the name of unbranched-chain isomers

A

Which carbon the branch is on e.g. 2 = 2-….
Number of carbons in the branch e.g. 1 carbon = methyl
Longest carbon chain e.g. 4 = propane

27
Q

4.23 What is the functional group of alkenes

A

C=C

28
Q

4.24 What is the general formula for alkenes

A

CnH2n

29
Q

4.25 Why are alkenes unsaturated hydrocarbons

A

Contains at least 1 double bond of carbon atoms and only carbon and hydrogen atoms

30
Q

4.28 How can bromine water be used to distinguish between an alkane and an alkene

A

Method:
Place 5 drops of hydrocarbon into test tube
Add 5 drops of bromine water

Results:
Hexane - orange
Cyclohexene- colourless …….
Alkenes react with bromine water causing it to decolourise, alkanes do not

31
Q

4.27 What does the reaction of alkenes with bromine produce

A

Ethene + bromine -> dibromoethane ( Loses double bond between carbons and 2 bromine replace 2 hydrogen)

Addition reaction