Type of Reaction/Mechanisms Flashcards by Anya Olsen

Q

Acyl Chloride to Ester

A

Esterification / Condensation

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Acyl Chloride to Carboxylic Acid

A

Hydrolysis

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Acyl Chloride to Amide

A

Nucleophilic addition elimination

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Carboxylic Acid to Acyl Chloride

A

Chlorination

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Carboxylic Acid to Ester

A

Esterfication

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Carboxylic Acid to Sodium Carboxylate Salt

A

Neutralisation

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

1° Amide to Carboxylic Acid

A

Hydrolysis

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Nitrile to Carboxylic Acid

A

Hydrolysis

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Aldehyde to Carboxylic Acid

A

Oxidation

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Carboxylic Acid to Alcohol

A

Reduction

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Ester to Alcohol

A

Hydrolysis

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Ester to Carboxylic Acid

A

Hydrolysis

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Alcohol to Ester

A

Esterification

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Alcohol to Carboxylic Acid

A

Full Oxidation (only 1°)

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Alcohol to Aldehyde

A

Partial Oxidation (only 1°)

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Aldehyde to Alcohol

A

Reduction

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Aldehyde to Hydroxynitrile

A

Nucleophilic Addition

Q

Nitrile to Amine

A

Reduction

Q

Amine to 2° or 3° Amide

A

Nucleophilic addition elimination

Q

Amine to Copper Complex Ion

A

Ligand Exchange

Q

Amine to Salts

A

Neutralisation

Q

Amine to 2°, 3°, 4° Amine

A

Nucleophilic Substitution

Q

Halogenoalkane to Amine

A

Nucleophilic Substitution

Q

Halogenoalkane to Nitrile

A

Nucleophilic Substitution

Halogenoalkane to Alcohol

Nucleophilic Substitution

Alcohol to Halogenoalkane

Nucleophilic Substitution

Alcohol to Ketone

Oxidation (only 2°)

Ketone to Alcohol

Reduction

Ketone to Hydroxynitrile

Nucleophilic Addition

Alkene to Alcohol

Hydration/Addition

Alkene to Hydroxyhalide

Addition

Alkene to Polymer

Addition Polymerisation

Alkene to Diol

Oxidation

Alkene to Alkane

Hydrogenation Reduction

Alkene to Dihalogenoalkane

Electrophilic Addition

Alkane to Halogenoalkane

Free Radical Substitution

Alkane to CO2, H2O + energy

Combustion

Halogenoalkane to Alkene

Elimination

Alkene to Halogenoalkane

Electrophilic Addition

Ester to Other Ester

Transesterification