ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
10th Edition
ISBN: 9781260008562
Author: Carey
Publisher: MCG
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Chapter 15.7, Problem 5P
Interpretation Introduction

Interpretation:

A series of equations for the synthesis of 2-phenyl-2-butanol from benzene and 2-butyne by using retrosynthetic analysis is to be written by showing all necessary reagents.

Concept introduction:

Grignard and organolithium reagents are nucleophilic. They react with carbonyl groups and form a new carbon-carbon bond.

In the first step, an alkoxymagnesium halide is formed. It is converted to the desired alcohol by reaction with aqueous acid.

If the carbonyl compound is ketone, the product formed is a tertiary alcohol.

Grignard reagents are prepared by the reaction of an alkyl halide with magnesium metal in the presence of a diethyl ether as a solvent.

In this reaction, the solvent must be anhydrous. Hence diethyl ether is used.

Hydration of alkynes in the presence of a mercury (II) salt produces ketones.

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The initial rates method can be used to determine the rate law for a reaction. using the data for the reaction below, what is the rate law for reaction? A+B-C - ALA] At (mot Trial [A] (mol) (MD 2 1 0.075 [B]( 0.075 mo LS 01350 2 0.075 0.090 0.1944 3 0.090 0.075 0.1350 Report value of k with two significant Figure
Compare trials 1 and 2 where [B] is constant. The rate law can be written as: rate = k[A][B]". rate2 0.090 = 9. rate1 0.010 [A]m 6.0m = 3m [A] m 2.0m

Chapter 15 Solutions

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