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Organic Chemistry
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In this experiment you will test the relative ease of
conversions of several alcohols into alkyl chlorides
with Lucas reagent (HCI + ZnCl2 ).
tertiary alcohols react immediately with Lucas reagent to
produce turbidity while secondary alcohols do so in five
minutes
.
Primary alcohols do not react appreciably with Lucas
reagent at room temperature
The reaction may occur by one of two mechanisms, SN1 or
SN2, depending on the structure of the R
group.
In either mechanism, the first step is a rapid protonation of
the alcohol to form an oxonium ion. What
happens next depends on the
nature of R. If R is a group that readily forms a carbocation,
then the slow, rate-determining step will
be the loss of a water molecule
from the oxonium ion. The carbocation then reacts rapidly
with a halide ion to form the alkyl halide. This mechanism,
called SN1
the mechanismfollows in the following manner
The Lucas test is a test in alcohols that is conducted to test and differentiate between the types of primary, secondary or tertiary alcohol. It uses the differences in reactivity of hydrogen halides and the three classes or types of alcohol. In the reaction the hydrxy group is replaced by chlorine. The time it takes in the appearance of turbidity is used as a measure for determining the class of alcohol. A primary alcohol generally implies that no reaction will occur, secondary alcohols result in the solution turning cloudy after a period of three to five minutes and if the solution immediately turns cloudy it signifies that the alcohol present is tertiary, benzyl alcohol or allyl alcohol.
Reagent used : zinc chloride (ZnCl2) in concentrated aqueous hydrochloric acid (HCl)











