Topic 7 - Organic chemistry Flashcards

1
Q

What is crude oil in as much detail as possible?

A
  • – Crude oil is a fossil fuel found in rocks formed from the remains of ancient biomass (plants and animals). It is a finite resource.
  • – Crude oil is a mixture of lots of different hydrocarbons, most of which are alkanes.
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2
Q

What is the general formula for the homologous series of alkanes? Also, what are the first four members of the series?

A

General formula:
C(n) H(2n+2)

First four members:

  • – Methane (CH4)
  • – Ethane (C2H6)
  • – Propane (C3H8)
  • – Butane (C4H10)

NOTE: alkanes have all C-C single bonds

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3
Q

How does fractional distillation work in terms of evaporation and condensation?

A
  • – Oil is heated until most of it turns to a gas which then enters a fractionating column.
  • – There is a temperature gradient in the column which is hot at the bottom and cool towards the top
  • – The longer hydrocarbons have higher boiling points and therefore condense into a liquid and drains out the fractionating column early on
  • – The shorter hydrocarbons have lower boiling points therefore they evaporate more and condense back into a liquid towards the top of the column where it is much cooler
  • – The result is that the crude oil mixture is separated into different fractions each with a similar number of carbon atoms and therefore similar boiling points.
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4
Q

What are the names and uses of the different fuels in a fractionating column from the bottom upwards?

A
  • – Bitumen: roads
  • – Heavy fuel oil
  • – Diesel: lorries
  • – Kerosene: aircrafts
  • – Petrol: cars
  • – LPG (Liquefied petroleum gas)
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5
Q

How do the properties of hydrocarbon change as the chain gets longer?

A

As the hydrocarbon chain gets longer:

  • – Boiling point increases
  • – It gets less runny so more viscous (gloopy)
  • – It gets less flammable
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6
Q

What is the word equation for the complete combustion of a hydrocarbon in oxygen?

A

Hydrocarbon + oxygen —> carbon dioxide + water (+energy)

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7
Q

What is cracking and why is it used? What are the products of cracking?

A

Cracking:

  • – The process of splitting up long-chain hydrocarbons into smaller more useful molecules.
  • – It is used as short-chain hydrocarbons make good fuels due to the fact they are flammable. They are also high in demand.
  • – The products of cracking are alkanes and alkenes.
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8
Q

What are the two methods of cracking? Explain them in detail.

A

Catalytic cracking:

  • – Heat long-chain hydrocarbons to vaporise them
  • – Pass the vapour over a hot powdered aluminium oxide catalyst
  • – The long-chain molecules split apart on the surface of the catalyst

Steam cracking:

  • – Vaporise the hydrocarbon
  • – Mix vapour with steam
  • – Heat to a very high temperature
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9
Q

How does modern life depend on the uses of hydrocarbons?

A
  • – Oil provides fuel for most transport
  • – Petrochemical industry uses hydrocarbons as feedstock to make new compounds for use in things like polymers, solvents, lubricants and detergents
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10
Q

Why are alkanes saturated and alkenes unsaturated?

A

In an alkane, each carbon atom forms four single covalent bonds whereas alkenes have a double carbon bond so they have two fewer hydrogen atoms and are unsaturated.

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11
Q

What is the general formula for alkenes? What are the first four alkenes and their formulas?

A

General formula: C(n)H(2n)

First four:

  • – Ethene: C2H4
  • – Propene: C3H6
  • – Butene: C4H8
  • – Pentene: C5H10
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12
Q

Alkenes undergo incomplete combustion as they require a huge amount of oxygen to combust completely. They burn in air with smoky yellow flames due to this incomplete combustion. What is the word equation of incomplete combustion with alkenes?

A

Alkene + oxygen —> carbon + carbon monoxide + carbon dioxide + water (+energy)

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13
Q

How do you test for alkenes?

A

Add bromine water to the solution. If the colour changes from orange to colourless then an alkene is present however if it stays bright orange then an alkane is present.

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14
Q

What is the functional group for an alkene? What reactions do alkenes undergo and what happens to the double carbon bond when it reacts?

A

Functional group: C=C

Alkenes undergo addition reactions. The C=C bond opens up to form a single carbon bond.

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15
Q

Describe the reaction and conditions for the addition of hydrogen, water and halogens to alkenes.

A

Addition of hydrogen:

  • – Double bond opens up to form a single bond
  • – Becomes a saturated alkane
  • – Reacts in the presence of a catalyst
  • – Known as hydrogenation

Addition of water/steam:

  • – Steam is added to the alkene then it is passed over a catalyst
  • – Forms an alcohol

Addition of halogen:

  • – Halogen such as bromine, chlorine or iodine is added to an alkene
  • – Forms saturated compund called di…
  • – e.g. bromine + ethene = dibromoethane
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16
Q

What is the general formula and functional group for alcohols? What are the first four alcohols and their formulas?

A

Functional group: -OH
General formula: C(n)H(2n+1)OH

First four alcohols:

  • – Methanol: CH3OH
  • – Ethanol: C2H5OH
  • – Propanol: C3H7OH
  • – Butanol: C4H9OH
17
Q

What happens when any of the first four alcohols react with sodium, burn in air, are added to water or react with an oxidising agent?

A
  • – When reacting with sodium, one of the products formed is hydrogen.
  • – When they burn in air, they undergo complete combustion to produce carbon dioxide and water
  • – When it is added to water, their solutions form a neutral pH.
  • – When it is oxidised, they produce a carboxylic acid
18
Q

What are the main uses of alcohols?

A
  • – Solvents in the industry

- – Fuels in spirit burners

19
Q

Ethanol is the alcohol found in alcoholic beverages. It is made using fermentation. Describe this process in as much detail including the reaction and conditions of fermentation.

A

Aqueous ethanol word equation:
sugar —> ethanol + carbon dioxide

— Fermentation uses an enzyme in yeast to convert sugars into ethanol

Optimum conditions:

  • – 37 degrees Celsius
  • – slightly acidic
  • – anaerobic conditions
20
Q

What is the functional group for carboxylic acids? What are the first four carboxylic acids and their formulas?

A

Functional group: -COOH

First four members:

  • – Methanoic acid: HCOOH
  • – Ethanoic acid: CH3COOH
  • – Propanoic acid: C2H5COOH
  • – Butanoic acid: C3H7COOH
21
Q

What happens when any of the first four carboxylic acids react with carbonates, dissolve in water or react with alcohols?

A

React with carbonates:
— Produce salt, water and carbon dioxide

Dissolve in water:
— Partially ionise and release H+ ions

React with alcohols:

  • – Produce esters (which have the functional group -COO) and water
  • – Reaction uses an acid catalyst
22
Q

What is addition polymerisation?

A

When multiple alkenes (unsaturated monomers) open up their double bonds and join together to form polymer chains.

23
Q

What is condensation polymerisation?

A

When monomers from two different functional groups react and join to lose a small molecule, usually water and are therefore called condensation polymerisation.

NOTE: Refer to another source for the symbol equation of condensation polymerisation

24
Q

What two functional groups do amino acids contain?

A

Basic amino group (NH2) and a carboxyl group (COOH)

p.s. The smallest and simplest amino acid is glycine