Answer:
the answer for that is false
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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The best and most correct answer among the choices provided by your question is the third choice or letter C.
The best model of a water <span>molecule would be: </span><span>Two small, plastic balls attached to a larger plastic ball by toothpicks</span>
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C. Sulfur and oxygen (non metals) forms a covalent bond while the magnesium (a metal) will react with both non metals to form an ionic bond