ORGANIC CHEMISTRY 3E WPNGC LL SET 1S 
ORGANIC CHEMISTRY 3E WPNGC LL SET 1S 
3rd Edition
ISBN: 9781119815792
Author: Klein
Publisher: WILEY
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Chapter 23.8, Problem 26ATS
Interpretation Introduction

Interpretation:

The stereochemical and regiochemical outcome for the given process should be discussed.

Concept Introduction:

Heck reaction: It describes the coupling reaction between aryl, vinyl or benzyl halide and alkene in presence of Pd catalyst.

    ORGANIC CHEMISTRY 3E WPNGC LL SET 1S , Chapter 23.8, Problem 26ATS

Consider elimination reaction where alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide.

The product of the elimination reaction is depends upon the β-positions of alkyl halide.  If the β-positions are identical and the products formed are also identical.  If the β-positions are different and the products formed are also different.  This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

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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.
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Chapter 23 Solutions

ORGANIC CHEMISTRY 3E WPNGC LL SET 1S 

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