ORGANIC CHEMISTRY (LL)-W/ACCESS
ORGANIC CHEMISTRY (LL)-W/ACCESS
10th Edition
ISBN: 9781259717536
Author: Carey
Publisher: MCG
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Chapter 28, Problem 28P
Interpretation Introduction

Interpretation:

A reaction mechanism for the preparation of bisphenol A is to be drawn and the structure of bisphenol B is to be predicted.

Concept Introduction:

Bisphenol A is a di phenolic compound.

The chemical reaction between phenol and acetone results in the formation of Bisphenol A.

The disodium salt of bisphenol A is used in the preparation of polycarbonates such as Lexan.

In acid-catalysis, the reaction occurs in the presence of an acid. Proton transfer takes place at the oxygen atom of carbonyl group and results in the formation of an electrophile which is better than the neutral carbonyl group.

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3b)Give the mechanisms for the following transformations:
Hydrocarbon X has the formula C6H12.X reacts with one molar equivalent of hydrogen in the presence of a palladium catalyst to form a product having 12 primary hydrogens.Treatment of X with ozone followed by zinc in aqueous acid gives a mixture two aldehydes.What is the structure of X?
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.
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