Answer:
I think it will option D hope it helps
I think the answer is a pure substance
The first step in the reaction is the double bond of the Alkene going after the H of HBr. This protonates the Alkene via Markovnikov's rule, and forms a carbocation. The stability of this carbocation dictates the rate of the reaction.
<span>So to solve your problem, protonate all your Alkenes following Markovnikov's rule, and then compare the relative stability of your resulting carbocations. Tertiary is more stable than secondary, so an Alkene that produces a tertiary carbocation reacts faster than an Alkene that produces a secondary carbocation.
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In order for the molecules to actually separate from each other, more energy must be added. This energy, called heat of fusion or heat of melting, is absorbed by the particles as potential energy as the solid changes to a liquid. I hope this helps
