ORGANIC CHEMISTRY-STD.WILEY PLUS CARD
ORGANIC CHEMISTRY-STD.WILEY PLUS CARD
3rd Edition
ISBN: 9781119340515
Author: Klein
Publisher: WILEY
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Chapter 23, Problem 62IP
Interpretation Introduction

Interpretation:

The synthesis of compound 1 has to be shown from alkenes 2 and 3.

Concept Introduction:

Simmons–Smith reaction: It involves reaction of alkenes with organozinc reagent namely ICH2ZnI which results in formation of three–membered ring in product.  This is a concerted reaction in which the configuration of starting alkene is preserved.

Swern oxidation: Primary and secondary alcohols undergoes oxidation reaction using dimethyl sulfoxide, oxalyl chloride and triethyl amine which provides aldehyde and ketones.

ORGANIC CHEMISTRY-STD.WILEY PLUS CARD, Chapter 23, Problem 62IP , additional homework tip  1

Wittig Reaction:

It is an organic reaction where an aldehyde or a ketone gets converted to an alkene by replacing carbonyl group by a C=C bond.  A phosphorous ylide is used for this conversion.  It is a neutral molecule where a positively charged phosphorous is attached to a negatively charged carbon atom.

  ORGANIC CHEMISTRY-STD.WILEY PLUS CARD, Chapter 23, Problem 62IP , additional homework tip  2

Grubbs catalyst: This catalyst is used to achieve alkene metathesis.  It contain transition metal namely Ru which is doubly bonded with carbon atom.

  ORGANIC CHEMISTRY-STD.WILEY PLUS CARD, Chapter 23, Problem 62IP , additional homework tip  3

Dienes in presence of Grubbs catalyst, alkene metathesis serve as method of ring formation.

ORGANIC CHEMISTRY-STD.WILEY PLUS CARD, Chapter 23, Problem 62IP , additional homework tip  4

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Chapter 23 Solutions

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