ORGANIC REAGENTS
[1]NAME OF REAGENT- PCC (Pyridinium Chloro Chromate)
CONDITION - Solvent -CS2
IT'S USE- Restricted Oxidation of Alcohol to form Aldehyde
[2]NAME OF REAGENT- Aqueous NaOH
IT'S USE- Nucleophilic Substitution, Converts Halo Alkanes to Alocohol
[3]NAME OF REAGENT- NaOH in Ethanol
IT'S USE- Elimination Reaction, Converts Halo Alkanes to Alkene
[4]NAME OF REAGENT- PCl5
IT'S USE- Chlorinating Agent, Reacts with OH group in Alcohols & Carboxylic acids
[5]NAME OF REAGENT- Mg in dry Ether
IT'S USE- Used to make grignard reagents from haloalkanes
[6]NAME OF REAGENT- Excess Conc. H2SO4
IT'S USE- Dehydrating Agent, used to dehydrate alcohols to alkenes
[7]NAME OF REAGENT- HNO3 & H2SO4
IT'S USE- Adds NO2 Group on to Benzene Ring
[8]NAME OF REAGENT- HCl and NaNO2
IT'S USE- Forms diazonium salts with Phenylamine
[2]NAME OF REAGENT- Aqueous NaOH
CONDITION - Reflux
IT'S USE- Nucleophilic Substitution, Converts Halo Alkanes to Alocohol
[3]NAME OF REAGENT- NaOH in Ethanol
CONDITION - Reflux
IT'S USE- Elimination Reaction, Converts Halo Alkanes to Alkene
[4]NAME OF REAGENT- PCl5
CONDITION - Room Temperature
IT'S USE- Chlorinating Agent, Reacts with OH group in Alcohols & Carboxylic acids
[5]NAME OF REAGENT- Mg in dry Ether
CONDITION - Reflux
[6]NAME OF REAGENT- Excess Conc. H2SO4
CONDITION - Heat
[7]NAME OF REAGENT- HNO3 & H2SO4
CONDITION - 550 C
IT'S USE- Adds NO2 Group on to Benzene Ring
[8]NAME OF REAGENT- HCl and NaNO2
CONDITION - Below 50 C
[9]NAME OF REAGENT - Cl2 and AlCl3
CONDITION - Warm gently
IT’S USE - Adds Cl group onto benzene ring
[10]NAME OF REAGENT - CH3CH2Cl
and AlCl3
CONDITION
- Warm gently
IT’S USE - Adds CH3CH2 group onto benzene ring
[11]NAME OF REAGENT - Cl2 (g)
CONDITION - Ultra Violet Light
IT’S USE - Free Radical Reaction,
Used to convert alkanes to haloalkanes
[12]NAME OF REAGENT - Br2 in
CCl4
CONDITION - Room temperature, in the Dark
IT’S USE - Electrophilic Addition,
Converts alkenes to dihaloalkanes
[13] NAME OF REAGENT - H2(g)
CONDITION – Nickel catalyst, 3000 C and 30 atmospheres pressure
IT’S USE - Hydrogenating Agent, used to
convert benzene to cyclohexane
[14] NAME OF REAGENT - H2(g)
CONDITION – Nickel catalyst, 1500 C
IT’S USE - Reducing Agent, used to
convert alkenes to alkanes
[15] NAME OF REAGENT - Tin in Hydrochloric acid
[15] NAME OF REAGENT - Tin in Hydrochloric acid
CONDITION – Reflux
IT’S USE - Reducing Agent for converting nitrobenzene to phenylamine