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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Vegetable soup should be the correct answer. The reason for this is that it can easily be split, where as the rest would be very difficault if not imposible because of chemical change.
100% find the gfm of both sides then divide
An object which experiences either a change in the magnitude or the direction of the velocity vector can be said to be accelerating. This explains why an object moving in a circle at constant speed can be said to accelerate - the direction of the velocity changes.
Answer:
pOH = 11.5
[H⁺] = 0.003 M
[OH⁻] = 3 × 10⁻¹² M
Explanation:
The computation is shown below:
Given that
pH = 2.5
Based on the above information
We know that
pH + pOH = 14 ⇒ pOH = 14 - pH
pOH = 14 - 2.5
pOH = 11.5
[H⁺] = 10^(-pH) = 10^(-2.5)
[H⁺] = 0.003 M
[OH⁻] = 10^(-pOH)
= 10^(-11.5)
= 3 × 10⁻¹² M
[OH⁻] = 3 × 10⁻¹² M
Hence, the above represents the answer
