ORGANIC CHEMISTRY WILEYPLUS ACCESS>I<
ORGANIC CHEMISTRY WILEYPLUS ACCESS>I<
4th Edition
ISBN: 9781119850151
Author: Klein
Publisher: WILEY
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Chapter 6, Problem 56IP

(a)

Interpretation Introduction

Interpretation: The migrating carbon atom and curved arrow for migration are interpreted for the given carbocation rearrangement.

  ORGANIC CHEMISTRY WILEYPLUS ACCESS>I<, Chapter 6, Problem 56IP , additional homework tip  1

Concept introduction: The chemical transformation can be shown by the arrow pushing method in which the curved arrows show the movement of electrons or protons. A carbocation is one of the intermediates that can rearrange to form a more stable carbocation. The stability order of carbocation is:

Tertiary > Secondary > Primary

(b)

Interpretation Introduction

Interpretation: The more stability of carbocation (2) compared to (1) is interpreted for the given carbocation rearrangement.

  ORGANIC CHEMISTRY WILEYPLUS ACCESS>I<, Chapter 6, Problem 56IP , additional homework tip  2

Concept introduction: The chemical transformation can be shown by the arrow pushing method in which the curved arrows show the movement of electrons or protons. A carbocation is one of the intermediates that can rearrange to form a more stable carbocation. The stability order of carbocation is:

Tertiary > Secondary > Primary

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bn 6. a.) Classify the following carbocations (1°, 2°, or 3°). b.) Encircle the carbocation/s that can rearrange to a more stable structure. smib-t.-S) CH3 CH3 CH3 CH2 CH2 CHz-C+ CH3
7. a) A) In the box below the arrow, label if the pericyclic reaction is a Diels Alder (DA), Electrocyclic (EC) or Sigmatropic Rearrangement (SR). B) Determine the major product(s). heat HO₂C b) heat to c) + 1. Na, NH3 NO2 NO2 2. heat
6. Rank the alkenes in order of increasing stability. (1 = least stable, 4 = most stable)
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