Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
2nd Edition
ISBN: 9780393655551
Author: KARTY, Joel
Publisher: W. W. Norton & Company
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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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When an unknown amine reacts with an unknown acid chloride, an amide with a molecular mass of 163 g/mol (M* = 163 m/z) is formed. In the infrared spectrum, important absorptions appear at 1661, 750 and 690 cm. The 13C NMR and DEPT spectra are provided. Draw the structure of the product as the resonance contributor lacking any formal charges. 13C NMR DEPT 90 200 160 120 80 40 0 200 160 120 80 40 0 DEPT 135 T 200 160 120 80 40 0 Draw the unknown amide. Select Dow Templates More Frage

Chapter 11 Solutions

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)

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