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

Q

Halogenoalkane to Alcohol

A

Nucleophilic Substitution

Q

Alcohol to Halogenoalkane

A

Nucleophilic Substitution

Q

Alcohol to Ketone

A

Oxidation (only 2°)

Q

Ketone to Alcohol

A

Reduction

Q

Ketone to Hydroxynitrile

A

Nucleophilic Addition

Q

Alkene to Alcohol

A

Hydration/Addition

Q

Alkene to Hydroxyhalide

A

Addition

Q

Alkene to Polymer

A

Addition Polymerisation

Q

Alkene to Diol

A

Oxidation

Q

Alkene to Alkane

A

Hydrogenation Reduction

Q

Alkene to Dihalogenoalkane

A

Electrophilic Addition

Q

Alkane to Halogenoalkane

A

Free Radical Substitution

Q

Alkane to CO2, H2O + energy

A

Combustion

Q

Halogenoalkane to Alkene

A

Elimination

Q

Alkene to Halogenoalkane

A

Electrophilic Addition

Q

Ester to Other Ester

A

Transesterification