Please correct answer and don't use hand raiting Chapter 6 Carbocation Rearrangement AssignmentThe most common carbocation rearrangements are a hydride shift and a methyl shift. Anothertype of carbocation rearrangement is an alkyl shift, which is typically possible when a structure involvesa small ring (with ring strain) and a carbocation that can be rearranged so that a more stable ring (5- or6-membered) is formed.Draw the mechanism that would account for the following carbocation rearrangement. For fullcredit, you must also number the carbons in both structures to accurately indicate the bonding betweeneach carbon.++

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Answered: Chapter 6 Carbocation Rearrangement…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 5E

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Which statement is false regarding the following system? + HX Addition Elimination H -X O A positive AG means that the equilibrium will favor the reactants because the entropy term is larger than the enthalpy term representing the gain of entropy when one molecule becomes two. O A negative AG means that the equilibrium will favor the products because the enthalpy term is larger than the entropy term representing the loss of entropy when two molecules become one. Elimination reactions are thermodynamically favored at high temperatures, where the entropy of the reaction will be larger than the enthalpy, causing a positive AG and the reactants to be favored over the products. Addition reactions are thermodynamically favored at high temperatures, where the entropy of the reaction will be larger than the enthalpy, causing a positive AG and the reactants to be favored over the products.
By taking into account electronegativity differences, draw the products formed by heterolysis of the carbon–heteroatom bond in each molecule. Classify the organic reactive intermediate as a carbocation or a carbanion.
Draw the rearrangement mechanism for the following image #10
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