Study Set Content:
n-butyl chloride is the fastest which means that the lesser the steric effect, the faster it reacts with SN2.
SN2 Rxn
- according to this rule, base-induced elimination reactions generally give the more stable alkene product—that is, the alkene with the larger number of alkyl substituents on the double bond.
Elimination Reaction: Zaitsev’s Rule
In the elimination of HX from an alkyl halide, the more highly substituted alkene product predominates.
In the elimination of HX from an alkyl halide, the more highly substituted alkene product predominates.
n-butylchloride other name
1-chlorobutane, butyl chloride, Chlorobutane, N-chlorobutane
n-butylchloride formula
C4H9Cl
sec-butylchloride
2-chlorobutane, secButylchloride, 1-methylpropyl chloride
sec-butylchloride formula
C4H9Cl
tert-butylchloride other name
Chlorotrimethyl methane, Trimethylchloromethane
tert-butylchloride formula
(CH3)3CCl
Chlorobenzene other name
Monochlorobenzene
solvent
Chlorobenzene
Solven,alkylating agent
N-butylchloride
Used to produce alcohols or alkoxide salts, Solvent
tert-butylchloride
Solvent for some pesticide formulations
To degrease automobile parts
Chemical intermediate
sec-butylchloride
N-butylchloride
sec-butyl chloride
tert-butyl chloride
Chlorobenzene
Beilstein test n-,sec-,tert-butyl chloride, chlorobenzene
Green flame
Reaction with 2%Ethanolic AgNO3 n-,sec-,tert-butyl chloride, chlorobenzene
Turbid solution in 30 secs, Turbid solution in 25 secs, White precipitate formed in 20 secs, Turbid solution in 50 secs
