EBK GET READY FOR ORGANIC CHEMISTRY
EBK GET READY FOR ORGANIC CHEMISTRY
2nd Edition
ISBN: 9780321830555
Author: KARTY
Publisher: VST
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Chapter 11, Problem 11.56P
Interpretation Introduction

Interpretation:

The complete, detailed mechanism for the reaction of but-1-ene-3-yne with HBr, producing 4-bromobuta-1, 2-diene is to be drawn.

Concept introduction:

The pi bond of an alkene or an alkyne is an electron-rich region. It undergoes electrophilic addition reaction when treated with a Bronsted acid. The addition of proton in the first step leads to the formation of a carbocation intermediate. The carbocation may undergo a rearrangement if it leads to a more stable carbocation. In the second step, the conjugate base of the acid adds to the carbocation.

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a. What is the eluent used in the column chromatography here (a “silica plug filtration” is essentially a very short column)? b. The spectroscopy of compound 5b is described in the second half of this excerpt, including 1H-NMR and 13C-NMR (which you will learn about in CHEM 2412L), MS (which you will learn about later in CHEM 2411L) and IR. One of the IR signals is at 3530 cm-1. What functional group does this indicate might be present in compound 5b?
Steps and explanations. Also provide, if possible, ways to adress this kind of problems in general.
a. The first three lines of this procedure describe the reaction used to make compound 5b. In the fourth line, hexane and sodium bicarbonate are added. What organic lab technique is being used here?  b. What is the purpose of the Na2SO4?  c. What equipment would you use to “concentrate [a solution] under reduced pressure”?

Chapter 11 Solutions

EBK GET READY FOR ORGANIC CHEMISTRY

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