ORGANIC CHEMISTRY-STUD.SOLNS.MAN+SG(LL)
ORGANIC CHEMISTRY-STUD.SOLNS.MAN+SG(LL)
4th Edition
ISBN: 9781119659587
Author: Klein
Publisher: WILEY
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Chapter 11, Problem 32ASP
Interpretation Introduction

Interpretation: To represent a logical retrosynthesis of the given diol target molecule.

Concept introduction:

  1,2 diols can be formed from diketones by reducing the two carbonyl groups using a variety of reducing agents such as NaBH4 , LiAlH4 , H2/Pd , etc., or by dihydroxylation of alkenes.

Thus, a vicinal diol can be prepared from an alkene starting material, and a trans alkene can be prepared from an alkyne.

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1. Base on this experimental results, how do you know that the product which you are turning in is methyl 3-nitrobenzoate(meta substituted product ) rather than either of the other two products?  2. What observation suggests that at least a small amount of one or both of the other two isomers are in the mother liquor?
Explain Huckel's rule.
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