6 Question (points) See page 574 Complete the mechanism. All necessary atoms and bonds (i.e. those...

Question

Question

Answer 1

Answer #1

Answer:

Explanation:

Migration of methyl group Ητα: step-1 I 20-carebocation. Double bond attacks H-a: Step-2 3-Carbocation Step-3 Ce binds to the

In step-1 the double bond attacks the H-Cl and gives rise to a 2°-carbication.

Then in step-2 migration methyl group to that positively charged carbon occurs thereby, generating a 3° carbocation.

This methyl group migrstion occurs so that a more stable 3°-carbocation can be generated.

And then in step-3 the Cl can attack to the 3°-carbocation and gives the product.

Answer 2

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