0% found this document useful (0 votes)
326 views

14 Lab Preparation of Chloroform

The document describes two methods for preparing chloroform in the laboratory: 1. By the distillation of a mixture of bleaching powder, water, and ethyl alcohol or acetone. The bleaching powder acts as a source of chlorine. 2. From ethyl alcohol in a three step process: oxidation to acetaldehyde, chlorination to chloral, then hydrolysis of chloral to produce chloroform and calcium formate. 3. From acetone in a two step process: chlorination of acetone to trichloroacetone followed by hydrolysis to chloroform and calcium acetate.

Uploaded by

Gamer's Tech
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
0% found this document useful (0 votes)
326 views

14 Lab Preparation of Chloroform

The document describes two methods for preparing chloroform in the laboratory: 1. By the distillation of a mixture of bleaching powder, water, and ethyl alcohol or acetone. The bleaching powder acts as a source of chlorine. 2. From ethyl alcohol in a three step process: oxidation to acetaldehyde, chlorination to chloral, then hydrolysis of chloral to produce chloroform and calcium formate. 3. From acetone in a two step process: chlorination of acetone to trichloroacetone followed by hydrolysis to chloroform and calcium acetate.

Uploaded by

Gamer's Tech
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 13

Wurtz Reaction

• In Wurtz’s reaction two alkyl group join together at


the site of halogen forming symmetrical alkane.
Two alkyl groups join together which are mirror
image of one another. e. g.,

2- Bromopropane
2-Chloro-2- methylpropane

2,2,3,3- tetramethyl butane


1- bromobutane

Br - + Na/ Ether
3

1- bromo-2- methylpropane

CHշ 3 +NaBr

2,5- dimethylhexane
Reduction
• Haloalkanes when reduced with reducing
agents such as,i) hydrogen in presence of Ni
or Pt or Pd catalyst OR ii) LiAlHч OR iii) Zn-
Cu couple in ethanol OR iv) Na in ethanol OR
v) Zn/Sn in conc HCl etc. produce alkane
containing the same number of carbon atoms
as it is in the parent haloalkane. For e. g.,
• Δ

Hշ Ni/Δ
HI
Finished
Monohalogen
Derivatives of alkane
Laboratory preparation of chloroform
• In the laboratory chloroform is prepared by
the distillation of a thin paste of bleaching
powder in water with ethyl alcohol or
acetone. Bleaching powder simply acts as a
source of chlorine and calcium hydroxide
required for the reaction
Principle:

CaOClշ +HշO = Clշ +Ca (OH ) շ


2
Bleaching powder
From ethyl alcohol
• The preparation of chloroform from ethanol
involves the following three steps.
1. Oxidation: In the first step ethyl alcohol oxidizes
into acetaldehyde.
CHȝCHշOH
+Clշ
Ethyl alcohol Acetaldehyde
OR OR
ethanol ethanal
2. Chlorination:
• The acetaldehyde thus formed undergoes
chlorination reaction and produces
trichloroacetaldehyde also known as chloral

3Clշ
Acetaldehyde Trichloroacetalldehyde
OR OR
ethanal Chloral
Or
trichloroethanal
3. Hydrolysis:
• Finally the chloral thus formed hydrolyzes with
calcium hydroxide and produces chloroform
together with calcium formate.

Calcium formate
Chloral Chloroform Or
OR Calcium methanoate
Trichloromethane
II) From acetone:
It involves the following two steps.

Acetone Trichloroacetone

Chloroform Calcium acetate


chlorofoem
R.B. flask
Water condenser

water
Adapter

Aq. layer
receiver

Laboratory preparation of chloroform


In a round

Water bath and heated until the


mixture of

You might also like