Topic 9 - Hydrocarbons, Alcohols, Carboxylic Acids, Polymers Flashcards

1
Q

hydrocarbons

A

molecular compounds that contain only carbon and hydrogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

alkanes general formula

A

CnH2n+2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

When are molecules saturated

A

When all the carbon-carbon covalent bonds are single bonds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

When are molecules unsaturated?

A

When they contain at least one double covalent bond between adjacent carbon atoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

alkenes general formula

A

CnH2n

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What bonds do alkenes have?

A

carbon-carbon double bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

isomers

A

Molecules with the same molecular formula, the different arrangements of atoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What do numbers in isomers show?

A

The position of the double bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is formed in the complete combustion of a hydrocarbon?

A

Only carbon dioxide and water is formed when there is a plentiful supply of oxygen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What gets produced in incomplete combustion?

A

If there is an insufficient amount of oxygen, full oxidisation does not occur and carbon (soot) and carbon monoxide can be formed as well as water and carbon dioxide

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

When and how is the bromine water test used?

A

To tell the difference between alkenes and alkenes because ALKANES do not react with it (cause decolourisation)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what and why is the colour change in the bromine water test if an alkene is detected

A

the orange-brown colour turns colourless because the C=C double bond reacts with the bromine to form a colourless product, bromine is therefore removed from the solution which looses it colour (hence why it doesn’t work with alkenes because they don’t have a double bond)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

addition reaction

A

Reaction in which reactants combined to form one larger product molecule and no other products

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

fermentation

A
  • Plant material containing sugars is mixed with water and yeast -> enzymes in the yeast, turn the sugars into ethanol and carbon dioxide
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What do the percentages mean in alcohols

A

How much ethanol they have

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How is ethanol made?

A

Through fermentation (sugars)

17
Q

Why is an airlock in the neck of a jar when making ethanol necessary (fermentation)?

A

Allow carbon dioxide to escape while keeping air out; this is necessary because yeast fermentation is a type of anaerobic respiration and only occurs in the absence of oxygen

18
Q

What is fractional distillation of an ethanol solution needed if the concentrations are higher than 15%?

A

Cause higher concentrations kill the yeast cell

19
Q

How is a fractional distillation column used for ethanol % above 15?

A
  • Ethanol boiling point (78°C) is lower than the boiling point of water (100°C)
  • The heated liquids evaporate and their vapour cool as they rise up the fractionating column
  • Cause the ethanol has a lower boiling point it remains a gas for longer and separates from the water -> as a result the first fraction that is collected contains a higher percentage of ethanol
20
Q

What do alkanes end in

A

-ane

21
Q

what do alkenes end in

A

-ene

22
Q

what do alcohols end in

A

-anol

23
Q

alcohol general formula

A

CnH2n+1OH

24
Q

Chemical properties of alcohols

A
  • Produces carbon dioxide and water on complete combustion
  • Can be oxidised to form compounds called carboxylic acid
  • Reacts with reactive metals, forming hydrogen gas is one of the products
25
Q

Functional group

A

The atom of group of atoms in a molecule that is responsible for its main chemical reactions

26
Q

Why do alcohols have similar chemical properties?

A

Because they all contain one -OH functional group

27
Q

What are the uses of alcohol?

A
  • solvents for cosmetics, medical drugs, varnishes
  • Methanol and ethanol a widely used fuels and can be made from renewable sources
28
Q

What is the method for the combustion of alcohols (CORE PRACTICAL)

A
  • Measure the mass of an alcohol burner and cap; record the mass and the name of the alcohol
  • Place the alcohol burner in the centre of a heat resistant mat
  • Using the measuring cylinder to add 100 cm³ of cold water to a conical flask
  • Measure and record the initial temperature of the water and clamp the flask above the alcohol burner
  • light the wick of the burner and allow the water to heat up by about 40°C
  • Replace the cap on the burner and measure and record the final temperature of the water
  • Measure the mass of the alcohol burner and cap again and record the mass
  • Calculate the mass of the alcohol burned to produce a 1°C rise in temperature
  • repeat all steps using fresh cold water and a different alcohol
29
Q

carboxylic acid general formula

A

CnH2n+1COOH

30
Q

How are carboxylic acids usually formed?

A

By the gentle oxidisation of alcohols using oxidising agents such as hot copper oxide

31
Q

What are the chemical properties of carboxylic acids?

A
  • form solutions with a pH less than 7 (if soluable)
  • React with metals to form a salt and hydrogen
  • React with bases to form salt and water
  • react with carbonates to form a salt, water and carbon dioxide
    -> acidic properties due to the presence of -COOH functional group