Alkynes can be reduced to alkenes using palladium charcoal catalyst deactivated with poison like sulphur compounds or quoline
Partially deactivated palladised charcoal isknown as Lindlar'scatalyst
Alkynes can also be reduced to alkenes with sodium in liquid ammonia (birchreduction)
From alkyl hallides
Alkyl can be prepared from alkyl hallide by treating with alcoholicpostash(potassium hydroxide dissolved in ethanol)
This reaction removes a molecule of Hx and therefore, the reaction involved is dehydrohalogenation
In this reaction, the hydrogenatom is eliminated from bcarbonatom C next to carbon which halogen is attached.
Therefore, this reaction is called Beliminationreaction
Nature of halogen atom andalkyl group determine rate of the reaction
It is observed that for halogens the rate is iodine > bromine > chlorine
While for alkyl groupfroups tertiary > secondary > primary
From vicinal dihalide
dihalogen derivatives of alkanes in which two halogens are attached adjacent carbon atom (called vicinal dihalide derivatives) are coneverted to alkenes by heating with zinc dust in ethylalcohol
From alcohol
Alkenes are prepared from alcohols by heating with protonic acid such as sulphuricacid at about 442k
this reaction is called as dehydration of alcohol
This reaction is also an example of b elimination reaction because Oh group takes out one hydrogen atom
From alcohol
Alkenes are prepared from alcohols by heating with protonic acid such as sulphuric acid at about 442 k
this reaction is called as dehydration of alcohol
This reaction is also an example of b elimination reaction because Oh group takes out one hydrogen atom