Organic Equations Flashcards

1
Q

Alcohol to Ester

A

Carboxylic Acid, conc H2SO4/H3PO4 or

Acyl Chloride or

Acid anhydride

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

The reaction of an alkane to haloalkane

A

Free radical substitution

Halogen

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

The reaction of haloalkane to amine

A

NH3 and Heat

Nucleophilic Substitution

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

Aldehyde to Carboxylic acid

A

K2Cr2O7 heat

Tollen’s reagent

Fehling’s solution

Reflux

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

Acylation of benzene

A

Acyl chloride/ acid anhydride

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

Alkyl hydrogen sulphate to Alcohol

A

Dilute and warm

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

Nitration of benzene

A

conc HNO3

conc H2SO4

50 degrees

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

2y Alcohol to ketone

A

Heat acidified potassium dichromate

K2Cr2O7

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

The reaction of an alkene to haloalkane

A

HX

X = halogen

Electrophilic addition

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

Haloalkane to Nitrile

A

Nucleophilic substitution

KCN dissolved in ethanol with heat

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

The reaction of Haloalkane to alkene

A

KOH

ethanol hot

Elimination

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

The reaction of an alkene to alkyl hydrogen sulphate

A

Conc H2SO4

Electrophilic Addition

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

The reaction of Alkene to Alcohol

A

H3PO4 + Steam/H2O

High temp and pressure

Hydration of alkene

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

phenylethanoate to phenyl ethanol

A

NaBH4

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

The reaction of Alcohol to an alkene

A

Dehydration

H2SO4

180 degrees

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

The reaction of Amine to Amide:

A

Acyl chloride

Dry

Nucleophilic addition to elimination

17
Q

Nitrile to Amine

A

LiAlH4 or

H2, Ni 200 degrees

Reduction of nitrile

18
Q

Alcohol to Aldehyde

A

Oxidation

[O]

Acidified potassium or sodium dichromate

The product should be syphoned away and cooled as produced

19
Q

Alkene to alkane

A

Hydrogenation

H2

Nickel catalyst

200 degrees

20
Q

Carboxylic acid to ester

A

Alcohol

conc H2SO4

21
Q

Nitrobenzene to phenylamine

A

Sn, conc HCl

then NaOH

22
Q

Aldehyde to 2-Hydroxynitrile

A

HCN

Nucleophilic Addition

23
Q

Aldehyde to Alcohol

A

Reduction of aldehyde

NaBH4

[H+]

24
Q

Phenylamine + acyl chloride/acid anhydride

A

forms N-phenylamide

25
Q

Benzene to cyclohexane

A

Hydrogenation

H2/

Nickel Catalyst

26
Q

Amine to Amide

Acid Anhydride

A

ACid anhydride

dry

Nucleophilic addition and elimination

27
Q

The reaction of haloalkane to alcohol

A

NaOH

Warm

Nucleophilic Substitution

28
Q

Ketone to 2-hydroxynitrile

A

HCN

Nucleophilic Addition

29
Q

Ketone to 2y Alcohol

A

NaBH4(aq)

30
Q

Nitrile to Amine

H2, Ni 200C

A

H2, Ni 200C or

LiAlH4

Reduction of nitrile