Organic Chemistry Flashcards

1
Q

Explain how a racemic mixture is formed

A

The molecule is planar so there is an equal probability of attack from above or below.

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

What are the advantages of recycling plastics?

A
  1. reduces landfills
  2. saves raw material
  3. lower cost of recycling than making from scratch
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the disadvantages of recycling plastics?

A

The process of collection, transportation and sorting is expensive.

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

How is Biodiesel made?

A

Oil is reacted with methanol to form a mixture of methyl esters and propane-1,2,3-triol

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

Why are the boiling points of amines lower than those of comparable alcohols?

A

Nitrogen is less electronegative than oxygen so the hydrogen bonds are not as strong as those in alcohols.

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

What is a inductive effect?

A

Alkyl groups release electrons away from the alkyl group and towards the nitrogen atom. This increases the electron density of the nitrogen atom, making it a better electron pair donor.

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

Why are primary alkylamines stronger bases than ammonia?

A

Inductive effect makes nitrogen a better electron pair donor.

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

Why are secondary alkylamines stronger bases than primary alkylamines?

A

Secondary alkylamines have 2 inductive effects and are therefore stronger bases.

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

Why are tertiary alkylamines not stronger bases than secondary alkylamines?

A

They are less soluble in water.

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

Why are polyalkenes non biodegradable?

A

Only strong, non-polar C-H and C-C bonds.

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

Why are polyesters and polyamides biodegradable?

A

Polar bonds which can be broken down by hydrolysis.

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

What is Nylon 6,6 made from?

A

1-6-diaminohexane and hexane-1,6-dicarboxylic acid

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

What is Kevlar made from?

A

Benzene 1,4-diamine and Benzene 1,4-dicarboxylic acid

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

Explain aromatic stability?

A

The electrons in the p-orbital of the benzene ring overlap and are delocalised. They form a region of electron density above and below the ring which makes the structure very stable.

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

What are the advantages of ethanoic anhydridge over ethanoyl chloride?

A
  1. Cheaper
  2. Less corrosive
  3. Does not react with water as readily
  4. Safer, by-product is ethanoic acid rather than HCl
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What type of reaction -> between acyl chlorides and acid anhydrides with nucleophiles?

A

Addition-elimination reaction

17
Q

What property of sodium salts allow them to be good cleaning agents?

A

Ionic, dissociate to form Na+ and RCOO-. RCOO- has two distinct ends: a long hydrocarbon chain which in non-polar and the COO- group which is polar and ionic. The hydrocarbon will mix with grease while the COO- mixes with water, allowing grease and water to mix.

18
Q

How do you name an ester?

A

The -oate group is based off of the carboyxlic acid.