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Explain Carbocation
The mechanism is a sequence of two Brønsted acid-base reactions. In the first (step a), the double bond is protonated to give a tertiary carbocation; in the second (step b), the carbocation loses a dissimilar proton to give the alkene. The equilibrium is driven to the right by the greater stability of the alkene product. (Why is it more stable?)
FTIR instrumentation
It is Hydrated Potassium Aluminium Sulfate [ KAl(SO4)2·12H2O ].
How to find atomicity
oxo process - Hydrocabon It is as well known as carbonylation or hydroformylation reaction. A group of alkene carbon monoxides and hydrogen. Elevated temperature and under pres
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