3.3.14 - Organic Synthesis Flashcards

1
Q

Synthesis pathways

A

Needed to convert starting materials into a target compound

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

Reasons for yield being low

A

Product is left in the reaction mixture
The reaction in incomplete of irreversible

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

Oxidising agent

A

Acidified potassium dichromate

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

Reducing agents

A

NaBH4
H2 and Nickel catalyst
Tin / HCl

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

Dehydrating agents

A

Al2O3
Acid

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

NaBH4

A

Reduces a carbonyl group C=O to an alcohol group C-OH

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

H2 and Nickel catalyst

A

Reduces a C=C double bond

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

Tin / HCl

A

Reduces NO2 to NH2

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

Al2O3

A

Pass vapour over it

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

Acid

A

Catalysed elimination by H3PO4

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

Benzene to phenylketone

A

Acylation

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

Acylation

A

Benzene to phenylketone

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

Benzene to nitrobenzene

A

Nitration

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

Nitration

A

Benzene to nitrobenzene

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

Nitrobenzene to an aromatic amine

A

Reduction

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

Reduction

A

Nitrobenzene to an aromatic amine

17
Q

Aromatic amine to an aromatic amide

A

Use of an acyl halide

18
Q

Use of an acyl halide

A

Aromatic amine to an aromatic amide