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