Organic Reagents Class 12

Organic Reagents and their uses/functions


S.No.

Name of Reagent

Use/Function

Example

1

HCl + ZnCl2 (Lucas Reagent)

Substitution of –OH by -Cl group (Alcohol to Alkyl Chloride)

2

HBr or NaBr +H2SO4

Substitution of –OH by -Br group (Alcohol to Alkyl Bromide)

3

Red P/X2, (X2 = Br2, I2)

Substitution of –OH by –Br/I group (Alcohol to Alkyl Bromide/Iodine)

4

SOCl2

Substitution of –OH by -Cl group (Alcohol to Alkyl Chloride)

5

PCl5

Substitution of –OH by -Cl group (Alcohol to Alkyl Chloride)

6

Cl2 / Br2 in UV light/hν/heat

Substitution of hydrocarbon by –Cl/Br via free radical mechanism (Alkane to Alkyl Chloride/Bromide)

7

HCl/HBr with alkene

Addition via Markovnikov’s rule (Alkene to Alkyl Chloride/ Bromide).


8

NaI/KI in dry acetone

Substitution of halogens by –I group (Alkyl halides to Alkyl Iodide)

9

NaNO2 + HCl / HNO2

1° Amine to diazonium salt

10

Aq. KOH/NaOH

Substitution by –OH group (Alkyl halide to Alcohol)

11

Ethanolic KCN/ NaCN

Substitution by –CN (Alkyl halide to Alkyl Cyanide)

12

Cl2/Br2 in Dark or CCl4

Alkene to vicinal dichloride / dibromide

13

AgCN

Substitution by –NC (isocyanide) group (Alkylhalide to Alkyl isocyanide)

14

KNO2

Substitution by –ONO (Alkyl halide to Alkylnitrile)

15

AgNO2

Substitution by –NO2 (Alkyl halide to Nitroalkane)

16

Alcoholic KOH/ NaOH

β-elimination reaction (Alkyl halide to alkene)

17

Cl2, Anhydrous AlCl3

Chlorination of aromatic compounds

18

Conc. HNO3 + Conc. H2SO4

Nitration of aromatic compounds

19

Conc. H2SO4

Sulphonation of aromatic compounds

20

CH3Cl + Anhydrous AlCl3

Methylation (alkylation) of aromatic compounds (Friedel Craft alkylation).

21

CH3COCl + Anhydrous AlCl3

Ethanoylation (acylation) of aromatic compounds (Friedel Craft acylation).

22

H2O, H+

Hydration of alkene to alcohol

23

H2, Ni/Pt/Pd

Hydrogenation of alkene to Alkane, Reduction of

Aldehyde to alcohol etc.

24

NaBH4

Mild reducing agent, Ketone to alcohol.

25

LiAlH4/ B2H6

Strong reducing agent, Carboxylic acid to Alcohol.

26

RMgX (Grignard Reagent)

Aldehydes and ketones to alcohols

27

Conc. H2SO4

Dehydration (Alcohols to alkene)

28

Acidified KMnO4 /Alkaline KMnO4/Acidified K2CrO7/ CrO3-H2SO4 (Jones reagent)

Strong oxidizing agent (Alcohols to Carboxylic acid)

29

CrO3/PCC

Mild oxidizing agent (Alcohols to aldehyde or ketone)

30

DIBAL-H

Strong reducing agent. (Cyanide to aldehyde, Ester to Aldehyde)

31

Br2 + NaOH

Hoffmann Bromamide Degradation reaction (Amide to Amine).

32

CHCl3 + 3KOH

Carbylamine reaction (Primary amine to Alkyl isocyanide)

 

By: Mr. Satyam Kumar Nigam

PGT Chemistry

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Comments

  1. Waiting for video explanation......thnkx for providing the soft copy of much easy notes(#of reagents)..will be helpful while revision......

    ReplyDelete

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