Get Ready for Organic Chemistry
Get Ready for Organic Chemistry
2nd Edition
ISBN: 9780321774125
Author: KARTY, Joel
Publisher: PEARSON
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Chapter 22, Problem 22.55P
Interpretation Introduction

Interpretation:

Compounds A-I in the given synthesis scheme are to be identified

Concept introduction:

Nitration is the aromatic electrophilic substitution reaction in the presence of concentrated nitric acid and concentrated sulfuric acid. In this reaction, nitronium ion NO2+ are attached to the aromatic ring and acts as an electrophile. Reagent Fe and HCl is converted nitrobenzene to aniline. Benzene undergoes aromatic electrophilic substitution with molecular bromine in the presence of a Lewis acid such as FeBr3 to yield bromobenzene. NaBH4 is a reducing agent that is used to convert the carbonyl carbon to alcohol.

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For this question, if the product is racemic, input both enantiomers in the same Marvin editor. A) Input the number that corresponds to the reagent which when added to (E)-but-2-ene will result in a racemic product. Input 1 for Cl, in the cold and dark Input 2 for Oy followed by H₂O, Zn Input 3 for D₂ with metal catalyst Input 4 for H₂ with metal catalyst B) Draw the skeletal structure of the major organic product made from the reagent in part A Marvin JS Help Edit drawing C) Draw the skeletal structure of the major organic product formed when (2)-but-2-ene is treated with peroxyacetic acid. Marvin 35 Help
Michael Reactions 19.52 Draw the products from the following Michael addition reactions. 1. H&C CH (a) i 2. H₂O* (b) OEt (c) EtO H₂NEt (d) ΕΙΟ + 1. NaOEt 2. H₂O' H H 1. NaOEt 2. H₂O*
Rank the labeled protons (Ha-Hd) in order of increasing acidity, starting with the least acidic. НОН НЬ OHd Онс

Chapter 22 Solutions

Get Ready for Organic Chemistry

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