Organic Chemistry (Triple) Flashcards

1
Q

What is the general formula for an alkane?

A
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2
Q

What is the general formula for an alkene?

A
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3
Q

By what method are the different parts of crude oil separated?

A

Fractional distillation

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4
Q

Fractions of crude oil are separated in fractional distillation, based on what property?

A

boiling point

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5
Q

Explain why longer-chain hydrocarbons have a higher boiling point.

A

Boiling point is dependent on the stength of intermolecular forces.

Larger molecules have stronger intermolecular forces.

This means that more energy is required to break them and so their boiling point is higher.

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6
Q

Outline how crude oil is formed.

A
  • Dead biomass falls to the ocean floor.
  • Layers of sediment build up on top of the dead biomass.
  • Over millions of years this creates huge pressure and heat.
  • After 100s of millions of years, crude oil has formed.
  • Crude oil can seep through porous rock and so rises.
  • It is trapped under a non-porous cap rock.
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7
Q

Why is crude oil described as a finite resource?

A

It forms much more slowly than it is being used up, and so it will run out.

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8
Q

Why is crude oil described as a feedstock?

A

Because the fractions of crude oil are used as raw materials in a number of industrial processes.

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9
Q

Define the term hydrocarbon

A

Molecules which are made up of hydrogen and carbon only.

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10
Q

Describe the process of fractional distillation.

A
  1. Crude oil is heated to 300-900 degrees.
  2. It enters the fractionating column, which is hotter at the bottom and cooler at the top.
  3. The very largest hydrocarbons with the highest boiling points may still be liquids at this temperature, and will be tapped out at the bottom of the column as bitumen.
  4. Other vapourised fractions rise, and will condense at different points through the column based on their boiling points, e.g. fuel oil, diesel, kerosene, petrol.
  5. At the top, some oil fractions may be small enough molecules to still be in gas form - these are tapped out at the top of the column as refinery gas.
  6. From top to bottom, the size of the molecules condensing and being tapped out of the column increase in size and boiling point.
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11
Q

Describe an alkane

A

Saturated hydrocarbon

General formula of CnH2n+2

Contains only single bonds

The first four are methane, ethane, propane, butane

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12
Q

Describe an alkene

A

Unsaturated hydrocarbon

General formula CnH2n

Contains at least one double bond

First three are ethene, propene, butene

Tested for with bromine water, which turns orange to colourless.

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13
Q

Describe the bromine water test for an alkene.

A

Bromine water (brown-orange) is added to the hydrocarbon.

An alkene has a double bond which allows it to react with the bromine.

The double bond breaks open, and two bromine atoms are joined to form a dibromo-alkane.

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14
Q

Why are alkanes comparatively unreactive as compared with alkenes?

A

Because alkanes are saturated - they have no bonds which are available to join with other substances.

Alkenes have a double bond which can be broken open and used to form new compounds with other substances.

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15
Q

Outline the hydrogenation of an alkene

A

This is the addition of hydrogen to an alkene.

Expt. conditions - 150 degrees and a nickel catalyst

Double bond breaks open and 2 hydrogens are added, forming an alkane.

Remember nickel is a catalyst, so at the end of the reaction you get your

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16
Q

What is a catalyst?

A

Something that speeds up a reaction without taking part in or, or being chemically changed itself.

17
Q

What is cracking?

A

Cracking is the breaking up of large hydrocarbons in shorter chain hydrocarbons.

The process produces one alkene and one alkane, with the total number of carbons in these equalling the number of carbons in the original large hydrocarbon.

18
Q

Why are large molecules cracked?

A

Because the smaller molecules that cracking produces are often more useful - perhaps as fuels or feedstock for other industrial processes.

There is much lower demand for very large hydrocarbons.

19
Q

Describe the hydration of ethene.

A

Ethene is reacted with steam.

The double bon breaks open.

This allows one hydrogen and one OH group to join.

The OH group is the functional group of the alcohols, so ethanol is produced.

20
Q

Name the two ways of producing an alcohol.

A

Fermentation and hydration of alkenes

21
Q

Describe alcohols

A

Alcohols contain an -OH group

The first four are methanol, ethanol, propanol and butanol

22
Q

Describe the solubility of alcohols in water

A

The smaller alcohols are completely soluble in water, but the solubility decreases as the number of carbons increases.

After 4 carbons, the alcohols will often form a separate layer when mixed with water.

23
Q

What happens to the viscosity of hydrocarbons as the chain gets longer?

A

As the hydrocarbon chain gets longer, the viscosity increases.

24
Q

Name the two types of cracking

A

steam cracking and catalytic cracking.

25
Q

what do alkanes produce when burned in air?

A

carbon dioxide and water if combustion is complete

If combustion is incomplete, then carbon monoxide or carbons (soot) may also be produced.

26
Q

How do alkenes burn in air?

A

In the same way as alkanes, although they tend to burn with a more yellow smokey flame, due to incomplete combustion.

27
Q

What is a reversible reaction?

A

One which can happen in two directions; the products can form the reactants again.

28
Q

In a reversible reaction, which direction will a high pressure favour?

A

whichever side has the fewest number of moles on it.

29
Q

In a reversible reaction, which direction will a high temperature favour?

A

Whichever direction is endothermic.

30
Q

Why are biofuels better for the environment than fossil fuels?

A

biofuels are derived from plants, which absorb carbon dioxide as they grow. This is released when they have been fermented and the derived alcohol burned. However, the net release od carbon dioxide is negligible.