This is an organic reaction that involves (Z)-3-methyl-pent-2-ene and Br2 in CH3OH.
What is the product?
We can see that this is an organic reaction that involves (Z)-3-methyl-pent-2-ene and Br2 in CH3OH. This reaction first involves the formation of a dibromo compound with the substrate via the brominium intermediate.
It is important to recall that like most of the organic reactions, wat takes place in the process just described here occurs in a sequence of steps and each step of the reaction tends to bring us closer to the end product of the entire steps of the reaction take in proper order which makes the reaction to make sense to any one that studies it.
The solvent now reacts with the dibromo compound to form a stable carbocation. We can see that the product as shown emanated from a stable tertiary carbocation which is then attacked by the -OH group to complete the reaction sequence.
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