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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?)
Which of the following halides has maximum melting point: (1) NaCl (2) NaBr (3) Nal (4
3-methylhexane impact name
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can you describe how the valance shell electron configuration affectst the reactivity of the elements in the lanthanides and actinides series?
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A solution is prepared with 3.85g of a non-ionic unknown compound in 100.0g cyclohexane. The solution had a freezing point of 4.18 degrees Celsius. What is the molar mass of the un
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