Unit 3 Flashcards

1
Q

What does it mean when something is unsaturated?

A

An unsaturated compound is a compound with at least one carbon — carbon double bond.

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

What does it mean when something is saturated?

A

A saturated compound is something containing 1 single carbon — carbon bond

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

What are the types of alcohols?

A

Primary - joined to the end of carbon chain, the -OH is attached to a carbon atom with at least two Hydrogen atoms (-CH²OH)

Secondry - joined to an intermediate carbon atom, the -OH is attached to a carbon atom that has only 1 hydrogen atom

Tertiary - joined to an intermediate carbon atom which also has a branch attached, -OH is attached to a carbon atom that dosn’t have any hydrogen atoms.

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

How do you get soap from edible fats and oils?

A

When edible fats and oils (esters) are hydrolysed, they produce glycerol and carboxylic acids (fatty acids). If you then have a hydrolysis reaction with an alkali (NaOH) the fatty acids form salts, this is now a soap.

Fat + alkali —–> glycerol + salt (soap)

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

Explain, in hydrocarbons why does the molecules size increase as the boiling point increases?

A

Bigger molecules = more electrons = stronger LDFs = more energy to break apart

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

What are essential oils?

A
  • essential oils are concentrated extracts of the aroma compounds found in plants.
  • widely used in perfumes, cosmetics and cleaning products as well as flavourings.
  • not the same as edible oils, contain more volatile and insoluble in water compounds, like isoprenes.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is a substitution reaction?

A
  • a substitution reaction is when an atom in the molecule substituted for another.
  • this is done in 3 steps; initiation, propagation and termination.

CH⁴ + Cl² ——> CH³Cl + HCl

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

What force is found between hydrocarbons?

A

The force between hydrocarbons is the intermolecular force that is LDF

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

What makes up a soap molecule?

A
  • They have hydrophilic heads which are water soluble

* They also have hydrophobic (hydrocarbon) tails which are soluble in oil and grease

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

How do you name molecules, using the systematic naming rule?

A
  1. Identify the (parent) compound with the longest chain, name the alkane, cycloalkane or alkane it is
  2. For alkane, start counting from the side with the carbon — carbon double bond
  3. For branches, name them according to carbons (methyl, etheyl)
  4. Where there are branches and double bonds that’s the lowest number of the chain
  5. Use the terms (di, tri, etc.) When describing two or three double bonds and branches of the same type
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How do hydrogen bond affect viscosity?

A

Hydrogen bonds make a compound more viscose.

More hydrogen bonds = higher viscosity

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

What can carboxylic acids be identified by?

A

Carboxylic acids can be identified by its carboxyl group, –COOH

       O
       ||
   — C –OH

These can be named using the systematic naming rule

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

Are alcohols polar or non-polar?

A

Alcohols are polar as so they dissolve in other polar liquids like water. They will not dissolve in water as it is non-polar.

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

What reactions occur when breaking and forming esters?

A

When an ester breaks down in water it forms an alcohol and carboxylic acid, this is ester hydrolysis.

Forming esters = condensation reaction

Breaking esters = hydrolysis reaction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Why do esters have low boiling points and are non-polar?

A

Unlike alcohols and carboxylic acids, esters do not contain a hydroxyl group (–OH). Therefore, esters contain cannot form hydrogen bonds to other esters, thus lower boiling points and they are non-polar so can’t dissolve in polar substances like water.

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

What functional group do alcohol contain?

A

Alcohols are carbon compounds that contain the hydroxyl functional group, –OH

17
Q

Why are antioxidants used in food?

A
  • common method of preventing oxidation involves the addition of an antioxidant to food.
  • antioxidants will oxidise in place of the compounds they have been added to protect.
18
Q

Where are emulsifiers commonly found and how are they formed?

A
  • They are common in food.

* many emulsifiers are formed by edible oils, they have at least one hydroxyl group.

19
Q

What are some examples of elisifiers?

A
  • milk

* mayonnaise

20
Q

What happens when you oxidise terpenes?

A

The oxidation of terpenes produces compounds that contribute to the flavour and aroma of spices derived from plants.

21
Q

What does the oxygen to hydrogen ratio show?

A
  • that oxidation occurs when there is an increase in the oxygen to hydrogen ratio.
  • reduction occurs when there is a decrease in the oxygen to hydrogen ratio.
22
Q

How can aldehyde and keystones be identified?

A

Aldehydes and keytones can be identified by the presence of the carbon — oxygen double bond, the carbonyl group

23
Q

Brjrjr

A

Aldehydes have the carbonyl group at the end of the chain with a H attached. Ketones have a carbonyl group joined but to the other carbon atoms and no hydrogen atoms attached.