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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?)
synthesis and uses of DDT and BHC
Why +ve P.F. gives nuclear instability where as -ve PF gives nuclear stability ?explain .
Q. Show Equilibrium expression for water? Ans. The equilibrium expression for water is equal to a constant, Kw. This constant is called the ion product of water and is equ
The energy of second Bohr orbit of the hydrogen atom is -328 kJ mol-1, hence the energy of fourth Bohr orbit would be: (1) - 41 kJ mol -1 (2) -1312 kJ mol -1 (3) -164
Antiaromaticity - Hydrocarbon Planar cyclic conjugated substances, less stable as compared to the relating acyclic unsaturated species are known as antiaromatic. Molecular orbi
Explain trend in variation of the atomic size properties from Boron and Thallium
how to calculate the styx code for the borane atom?
How scale and sludge formed in boilers explain in kannKan
#bonding in KO2question..
Explain enantiomer
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