ORGANIC CHEMISTRY LL >BI<
ORGANIC CHEMISTRY LL >BI<
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ISBN: 9781260561609
Author: Carey
Publisher: MCG CUSTOM
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Chapter 13.16, Problem 23P
Interpretation Introduction

Interpretation:

The compounds A to C that is formed and the reagent that is used in each step during the retrosynthesis of the given compound is to be determined.

Concept introduction:

The addition of alkyl group to benzene results in the formation of alkyl benzene is done through Friedel Craft alkylation reaction.

In this reaction, the interference of a Lewis acid is required to initiate the respective reaction by withdrawing the halogen from an alkyl halide and make it an activated electrophile

This electrophile attacks on benzene ring and results in the alkylation of benzene ring along with the removal of respective hydrogen halide.

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Suggest possible synthetic route for following transformations. Show the reagents, intermediates and products.
A synthetic organic molecule, G, which contains both aldehyde and ether functional groups, is subjected to a series of reactions in a multi-step synthesis pathway. In the first step, G undergoes a Wittig reaction, leading to the formation of an alkene, H. Subsequently, H is treated with an ozone (O3) reagent followed by a reducing agent in an ozonolysis reaction, resulting in the formation of two different products, I and J. Considering the functional groups present in G and the nature of the reactions involved, what are the most probable structures or functional groups present in products I and J? A. I contains a carboxylic acid group, and J contains an aldehyde group. B. I contains a ketone group, and J contains an alcohol group. C. I and J both contain aldehyde groups. D. I contains an ester group, and J contains a ketone group. Don't use chat gpt.
Write a reaction equation sequence for the following synthetic conversion. Eachreaction step must be represented by a complete reaction equation in which substrate,reagents and products are shown. Mechanisms are not required.

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ORGANIC CHEMISTRY LL >BI<

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