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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3:6:2 is the correct answer
, THR CC14 formed in the first step is used as the reactant used in the second step.if 5.00 mol of CH4 reacts, what is the total amount of HCI producded. assume that C12 an HR in the presentin excess
I just looked it up and I found this:
Polar substances are likely to dissolve in polar solvents
Hope this helps!
Group of tissues form a cell , and a group of cells form an organ
