Name Reactions Flashcards by Samarth Sahu

Q

Rosenmunds reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

frinkelstein reactions

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

wolf kishner reaction and for what thing can it not be used

A

base sensitive stuff

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

balz scheimann reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

clemmenson’s reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

wittig reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

corey house synthesis

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

aldol condensation reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Cannizaro reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

hans diecker reactoin

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Hoffman Ammonolysis

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Gabriel Phthalimide synthesis

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Hoffman Bromamide Reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Hoffman Elimination of Quaternary Ammonium Salts

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Carbylamine Test

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Hoffman Mustard Oil test

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Diazonium Formation Reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Decarboxylation reaction with soda lime

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

HVZ reaction of halogen addition to carbo acid

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Gatterman Koch Reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Etards Reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Ninhydrin Test

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Intramolecular Aldol Condensation

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Perkin Reaction

A

How well did you know this?

1

Not at all

2

3

4

5

Perfectly

Q

Bayer Villager Oxidation Reaction

A

Q

Hydroboration Oxidation Reaction

A

Q

Oxymercuration and Demercuration Reaction

A

Q

Pinacol Pinacalone Rarrangement

A

Q

Victor Meyer Test

A

Q

Fishcher Esterification Reaction

A

Q

Lucas Test

A

Q

Williamson Synthesis Reaction

A

Q

Reimar Teimar Reaction

A

Q

Kolbe’s Carboxylation Reaction

A

Q

Sandmeyer’s Reaction

A

Q

stephens reduction

A

Q

wurtz reaction

A

Q

fittig reaction

A

Q

swartz reaction

A

Q

haloform reaction

A

Q

gattermann reaction

A

Q

friedal craft alkylation

A

Q

freidal craft acylation

A

carbon has octet complete in the intermediate

Q

esterification reaction

A

Q

Kolbe’s electrolysis reaction

A

Q

decarboxylation reaction

A

Q

Alcohol with Acid

A

Q

Bromination reaction under CCl4

A

BR goes from down and forms non classical carbocation and the other bromine then approached from the above and forms the di halide in anti addition manner

Q

Alkene with Peroxides

A

Q

Ozonolysis reaction

A

Q

Dehalogenation in presence Alc KOH and NaNH2

A

we can make a alkyne with di halide with alc KOH and NaNH2

if only Alc KOH ! then only alkene

Q

oxymercuration reaction with alkyne

A

Hg2+ loosens up the electron system in triple bond and makes it easier to attack

Q

treating alkyne with HBr in exccess

A

Q

Diazonium Salt formation reaction

A

NaNO2 and HCl is insitu to form HNO2

Q

halogenation of aromatic HC with FeCl3/AlCl3

A

Q

treating halide with KNO2

A

Q

alkyl Halide with AgNO2

A

Q

Grignard’s reagent with H2O

A

Q

aromatic Nucleophilic Sub of OH-

A

Q

Nitrogenation of benzene halide

A

Q

Sulphonation Reaction of Benzene

A

SO3 acts as an attacking agent