Harbor Process And Organic Chemistry Flashcards

1
Q

What happens if a reversible reaction takes place in a closed system*?

A

The reaction will reach a state of equilibrium which means the amounts of reactants and products will reach a certain balance and stay there.
(A closed system means the substances can’t escape)

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2
Q

What directions do the reactions go in a reversible reaction?

A

The reactions take place in both directions but the overall effect is nil because the forward and reverse reactions cancel each other out.

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3
Q

At what rate do the reactions take place in, in a reversible reaction?

A

The reactions take place at exactly the same rate in both directions.

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4
Q

In a reversible reaction what does the position of equilibrium depend on?

A

The temperature and pressure surround the reaction.

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5
Q

What happens when you alter the temperature/pressure of a reversible reaction?

A

You can move the position of equilibrium to give more product and less reactants.

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6
Q

What happens if you raise the temperature in a reversible reaction?

A

The endothermic reaction will increase to use up the extra heat.

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7
Q

What happens if you decrease the temperature in a reversible reaction?

A

The exothermic reaction will increase to give out more heat.

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8
Q

How is volume distributed in a reversible reaction?

A

Many reactions have a greater volume on one side, either of products or reactants.
(A greater volume means there are more gas molecules)

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9
Q

How does raising the pressure effect an reversible reaction?

A

It encourages the reaction which produces less volume.

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10
Q

How does lowering the pressure effect an reversible reaction?

A

It will encourage the reaction which produces more volume.

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11
Q

How does a catalyst effect a reversible reaction?

A

The catalyst speeds up both the forward and backward reactions by the same amount.
So the reaction will reach equilibrium quicker.

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12
Q

What reacts to form ammonia?

A

Nitrogen and hydrogen.

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13
Q

How are the products for ammonia productions obtained?

A

Nitrogen is obtained easily from the air.

Hydrogen comes from natural gas or other sources like crude oil.

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14
Q

What time of reaction is nitrogen and hydrogen?

A

Some of the nitrogen and hydrogen reacts to form ammonia but as it is reversible ammonia breaks down back into nitrogen and hydrogen.

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15
Q

What are the optimum industrial conditions for the haber process?

A
Pressure = 200 atmospheres
Temperature = 450 degrees
Catalyst = iron
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16
Q

What compromises are made for te conditions in the haber process?

A

The pressure is set as high as possible to give the best % yield without making the plant to expensive so it is set at 200 atmos.
The yield of ammonia would be greater at lower temperatures however this means a lower reaction rate so they increase the reaction anyway to get a faster rate of reaction.

17
Q

Why do higher pressures favour the forward reaction in the haber process?

A

Since there are four molecules of gas on the left side(greater volume) for every two on the right(less volume) meaning the reaction will go forward.

18
Q

Why would the yield of ammonia be greater at lower temperatures?

A

As the forward reaction is exothermic, which means the increasing temperature will move the equilibrium the wrong way (away from ammonia towards H2 and N2)

19
Q

Why is the iron catalyst important in the haber process?

A

Without the catalyst the temperature would have to be raised even further to get a quick enough reaction and that would reduce the % yield even further.

20
Q

What is a reversible reaction?

A

A reaction where the products of the reaction can themselves react to produce the original reactions.

21
Q

What is the general formula of an alcohol?

A

C(n)H(2n+1)OH

22
Q

What is the functional group of an alcohol?

A

C-OH

23
Q

What is the homologous series?

A

A group of chemicals that react in a similar way because they have the same functional group.

24
Q

What are the first three alcohols?

A

Methanol (1 carbon)
Ethanol (2 carbon)
Propanol (3 carbon)

25
Q

What are the properties of the first three alcohols?

A

Alcohols are flammable, they burn in air to produce carbon dioxide and water.
They all dissolve completely in water to form neutral solutions.
They also react with sodium to give hydrogen and alkoxides.

26
Q

Why are alcohols useful solvents?

A

Alcohols can dissolve substances water can’t such as hydrocarbons, oils and fats.

27
Q

What is methylated spirit?

A

Ethanol with chemicals added to it.

It’s used to clean paint brushes and as a fuel.

28
Q

What is the functional group of a carboxylic acid?

A

-COOH

29
Q

What is the naming system for alcohols?

A

Replace the last ‘e’ with ‘ol’

30
Q

What is the naming system for carboxylic acids?

A

Start with ‘meth/eth/prop’ and end in ‘-anoic acid’.

31
Q

What happens when carboxylic acids react with carbonates?

A

They react with carbonates to produce carbon dioxide.

The salts formed in these reactions end in ‘-anoate’.

32
Q

What happens when carboxylic acids dissolve in water?

A

They dissolve in water to produce acidic solutions.

When they dissolve they ionise and release H+ ions which are responsible for making the solution acidic.

33
Q

Why do carboxylic acids produce weak acidic solutions?

A

When they dissolve in water they ionise and release H+ ions but they don’t ionise completely (meaning not many H+ ions are released).
This means they have a higher pH so less acidic than other solutions of strong acids.

34
Q

What is the difference between strength and concentration of an acid?

A

Concentration is how watered down your acid is.

Strength is how well it had ionised in water.

35
Q

What can carboxylic acids be used for in industry?

A

Carboxylic acids with longer chains of carbon atoms are used to make soaps and detergents.
Carboxylic acids are also used in the preparation of esters.
Ethanoic acid is used as a solvent for many organic molecules.

36
Q

What is the equation to form an ester?

A

alcohol + carboxylic acid ➡➡➡ ester +water

37
Q

What is the naming system for esters?

A

Their names end in ‘-oate’
The alcohol forms the first part of the esters name and the acid forms the second part.
E.g. Methanol + propanic acid➡
Methyl propanoate + water

38
Q

What are the problems with esters?

A

Inhaling the fumes from some esters irritates mucous membranes in the nose and mouth.
Ester fumes are heavier than flames and very flammable.
Some esters are toxic, especially in large doses.

39
Q

What are the advantages of esters?

A

They smell nice so can be used in perfumes.
Also used to make flavourings and aromas.
Some esters can be used as solvents for paint, ink, glue and are less toxic and volatile than other organic solvents.