ORGANIC CHEMISTRY-STUDY GDE./SOL.MAN.
ORGANIC CHEMISTRY-STUDY GDE./SOL.MAN.
6th Edition
ISBN: 9780072397475
Author: SMITH
Publisher: MCG
Question
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Chapter 21, Problem 36P
Interpretation Introduction

(a)

Interpretation: The major enolate formed by the treatment of given compound with LDA is to be identified.

Concept introduction: Lithium diisopropylamide (LDA), molecular formula [(CH3)2CH]2NLi is a strong base and has been widely accepted due to its good solubility in non-polar organic solvent. It is a bulky base which usually extracts hydrogen from less hindered carbon.

Interpretation Introduction

(b)

Interpretation: The major enolate formed by the treatment of given compound with LDA is to be identified.

Concept introduction: Lithium diisopropylamide (LDA), molecular formula [(CH3)2CH]2NLi is a strong base and has been widely accepted due to its good solubility in non-polar organic solvent. It is a bulky base which usually extracts hydrogen from less hindered carbon.

Interpretation Introduction

(c)

Interpretation: The major enolate formed by the treatment of given compound with LDA is to be identified.

Concept introduction: Lithium diisopropylamide (LDA), molecular formula [(CH3)2CH]2NLi is a strong base and has been widely accepted due to its good solubility in non-polar organic solvent. It is a bulky base which usually extracts hydrogen from less hindered carbon.

Interpretation Introduction

(d)

Interpretation: The major enolate formed by the treatment of given compound with LDA is to be identified.

Concept introduction: Lithium diisopropylamide (LDA), molecular formula [(CH3)2CH]2NLi is a strong base and has been widely accepted due to its good solubility in non-polar organic solvent. It is a bulky base which usually extracts hydrogen from less hindered carbon.

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1600° 1538°C 1493°C In the diagram, the letter L indicates that it is a liquid. Indicate its components in the upper region where only L is indicated. The iron-iron carbide phase diagram. Temperature (°C) 1400 8 1394°C y+L 1200 2.14 y, Austenite 10000 912°C 800a 0.76 0.022 600 400 (Fe) a, Ferrite Composition (at% C) 15 1147°C a + Fe3C 2 3 Composition (wt% C) L 2500 4.30 2000 y + Fe3C 727°C 1500 Cementite (Fe3C) 1000 4 5 6 6.70 Temperature (°F)
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Part II. Given below are the 'H-NMR spectrum at 300 MHz in CDC13 and mass spectrum using electron ionization of compound Brian. The FTIR of the said compound showed a strong peak at 1710 cm"). Determine the following: (a) molecular Formula and Degree of unsaturation of compound Brian (b) Basing on the given H-NMR spectrum tabulate the following (i) chemical shifts (ii) integration, ciii) multiplicity and (iv) interferences made for each signal (c) Draw the structure of compound Brian. ) ΕΙ 43 41 27 71 114 (M+) Hmmm 20 30 40 50 60 70 80 90 100 110 120 1H NMR spectrum 300 MHz in CDCl3 2.0 alle 1.0

Chapter 21 Solutions

ORGANIC CHEMISTRY-STUDY GDE./SOL.MAN.

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