ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT
ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT
2nd Edition
ISBN: 9781119288510
Author: Klein
Publisher: WILEY
Question
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Chapter 4, Problem 67IP

(a)

Interpretation Introduction

Interpretation:

The more stable compound from given compounds cis-1,2-dimethylcyclopropane, trans-1,2-dimethylcyclopropane has to be identified.

Concept introduction:

  • Cyclopropane compounds are the smallest cyclic compounds.
  • The atoms are very closely located in cyclopropane compounds.
  • Every atoms/groups attached to the carbon atoms of cyclopropane are eclipsing in below the plane and above the plane.
  • The increasing cost energy order of eclipsed atoms/groups is,

H/H (4 kJ/mol) < H/CH3(6 kJ/mol) < CH3/CH3(11 kJ/mol)

(b)

Interpretation Introduction

Interpretation:

The energy difference between the two compounds has to be predicted.

Concept introduction:

  • Cyclopropane compounds are the smallest cyclic compounds.
  • The atoms are very closely located in cyclopropane compounds.
  • Every atoms/groups attached to the carbon atoms of cyclopropane are eclipsing in below the plane and above the plane.
  • The increasing cost energy order of eclipsed atoms/groups is,

H/H (4 kJ/mol) < H/CH3(6 kJ/mol) < CH3/CH3(11 kJ/mol)

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く Predicting the pr Predict the major products of the following organic reaction: Δ Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. ? Click and drag to start drawing a structure.
propose synthesis

Chapter 4 Solutions

ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT

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