Propanone, the simplest ketone compound can be reduced to a secondary alcohol by a reduction reaction. There are several reducing agents which are capable of reducing ketone to secondary alcohol. Then. secondary alcohol is dehydrated to propene by a dehydrator in this organic conversion.
In this tutorial, we are going to learn followings.
Following reagents can be used as reducing agents in the reduction of ketones to secondary alcohols.
LiAlH4 is the strong oxidizing agent. When propanone reacts with LiAlH4, 2-propanol which is a secondary alcohol is given as the product.
2-propanol is a secondary alcohol. When secondary alcohol is heated with a dehydrator, an alkene compound is given as the product.
With following dehydrators, reacting mixture should be heated. But, temperature depend on the used dehydrator.
When 2-propanol is heated with concentrated H2SO4 acid, a water molecule is eliminated to give propene.
Already you have seen how propanone is reduced to an alcohol compound by lithium aluminium hydride or other reducing agent. Now, we are going to see, another way of propanone reduction.
When propanone is reduced by clemmensen reduction reaction, propane is given. Propane is an alkane compound. As the clemmensen reagent, zinc amalgam and concentrated hydrochloric acid ( Zn(Hg) / conc. HCl ) is used.
Propene can be converted to propanone by two steps.