how is the catalytic hydration of alkenes an electrophilic addition reaction
A carbocation is formed and a electrophile is involved
what are two methods used in the hydration of alkenes
-the industrial method
-the laboratory method
what catalyst and conditions are used in the industrial method
steam(water vapour) is passed over the alkene in the presence of the H3PO4 catalyst adsorbed on sillica. It occurs under high temperature(573K) and pressure (60atm)
whats the name for the industrial method
steam cracking hydration
1) how is the electrophile produced
H3PO4 dissasoociates and provides a H+ ion which acts as an electrophile. The electron pair from the Pi bond attack it (protonation)
what are the three ways in which an electrophile can be produced
-via an acid
-via permenant dipole
-via temporary induced dipoel causes by C=C bond
why dont any electrons move onto H2PO4
H+ doesnt have any electrons
2) what happens to the carbon atoms in the C=C bond
one bonds to hydrogen and one becomes a carbocation
3) what acts as a nucleophile
water(the O atom in the molecule) acts as a nucleophile and attacks the carbocation
4) how is ethanol produced
H2PO4- accepts a proton to produce ethanol, regenerating the acid catalyst(deprotonation)
what catalyst and conditions are used in the laboratory method
concentrated H2SO4, water, heating and room temperature(293K) and pressure (100KPa)
what do we called the laboratory method
acid-catalysed hydration
what are the steps
the same as industrial just a different acid
what type of hydration has a higher yield
the industrial method because high temperature favours the forwards reaction, 95% yield vs 5% lab yield
hydration turns an alkene into an alcohol
alkene