Equilibria - Calthorpe Park Moodle

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Equilibria

Reversible Reactions

• In Reversible Reactions the products can react to form the original reactants

• Equilibrium reactions refer to the forward reaction (left to right) and the backwards reaction

• A reversible arrow is used

Reaction conditions

• An equilibrium only occurs if the reaction is in a closed system where nothing can get in or out.

• In a dynamic equilibrium the forward reaction and the backwards reaction occur at the same time and rate.

Industry

• Changing the reaction conditions, changes the equilibrium position and therefore the amount of reactants or products.

• This is important in industry where many products are made in equilibrium reactions.

The Haber Process

• Ammonia is made by the Haber Process

• Nitrogen + Hydrogen

Ammonia

N

2

+ 3 H

2

2 NH

3

• Nitrogen is from the fractional distillation of air and Hydrogen is obtained from methane.

Conditions for the Haber Process

• A high temperature increases the rate of reaction, but reduces the yield of Ammonia because the forward reaction to make ammonia is exothermic.

• A high pressure increases the rate of reaction, but is too expensive.

• Increasing the pressure favours the side of the equilibrium with the least number of gaseous molecules.

• Compromise temperature are used.

450 o C and 200 atm pressure

Economics of the Haber Process

• Using an Iron catalyst does not affect the position of the equilibrium, but it increases the rate of reaction and reduces the cost of the process. Iron is a cheap catalyst.

• Ammonia is cooled, liquefied and removed as soon as it is made to stop it decomposing.

• Unreacted Nitrogen and hydrogen are recycled.

• Ammonia is used to make fertilisers.

Organic

Chemistry

C

2

H

5

OH

Hydrocarbons

• Organic molecules contain carbon compounds

• Alkanes and Alkenes are hydrocarbons

• Ethane, C

2

H

6

Ethene, C

2

H

4

Functional Groups

• A functional group is the part of the molecule that is involved in chemical reactions.

• Replacing an H atom with a functional group makes other organic compounds:

• Alcohols, Carboxylic acids, Esters

-

OH

-

COOH

-

COO R

Alcohols

• Alcohols are a homologous series of compounds containing the

OH group.

• Ethanol, with a structural formula of C

2

H

5

OH.

• Displayed formula

• Ethanol is the alcohol found in drinks.

Properties of Alcohols

• They are Flammable and used as fuels

• Combustion of Ethanol :

C

2

H

5

OH + 3O

2

→ 2CO

2

+ 3H

2

O

• They react with Sodium to produce

Hydrogen, but this is slower than sodium with water.

Oxidation of Alcohols

• They can be oxidised to Carboxylic acids by boiling with potassium dichromate

• E.g. Ethanol makes Ethanoic acid (Vinegar)

Carboxylic Acids

• These are weak acids with pH values higher than for strong acids.

• Strong acids are fully ionised, but weak acids are partially ionised.

CH

3

COOH

CH

3

COO

-

+ H

+

• Weak acids have a lower concentration of

Hydrogen ions, H

+

.

Esters

• Carboxylic acids and Alcohols react to make

Esters.

• Carboxylic acid + Alcohol → Ester + Water

Ethanoic acid + Ethanol → Ethyl ethanoate + Water

CH

3

COOH + CH

3

CH

2

OH →CH

3

COOCH

2

CH

3

+ H

2

O

Concentrated Sulphuric acid is the catalyst.

Properties of Esters

• Ethanoic acid + Methanol

Methyl ethanoate + Water

• Esters are volatile – evaporate easily.

• They are sweet smelling and fruity.

• Uses include as perfumes and food additives

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