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The answer is maybe reactivity
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According to markovnikov's rule of the electrophilic addition to an alkene, the electrophile, usually a proton, is more likely to add to the less-substituted carbon in a double bond.
With additional substituents present in this configuration, the intermediate carbocation is stabilised by being located on the more-substituted carbon.
The nucleophile will then end up in a double bond on the more-substituted carbon in a reaction that follows Markovnikov's rule.The outcome of some addition reactions is described by Markovnikov's rule or Markownikoff's rule in organic chemistry. Vladimir Markovnikov, a Russian scientist, created the rule in 1870.
To learn more about Markovnikov's rule
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compound is formed .............
I know it would be calcium chloride, not sure why. Maybe someone could answer that part.
