ORGANIC CHEMISTRY (LL)-PACKAGE
ORGANIC CHEMISTRY (LL)-PACKAGE
8th Edition
ISBN: 9781319316389
Author: VOLLHARDT
Publisher: MAC HIGHER
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Chapter 8.8, Problem 8.21TIY

(a)

Interpretation Introduction

Interpretation: The synthesis of 2-methyl-2-propanol from methane should be written.

Concept introduction: Retrosynthetic analysis involves transformation of target molecule into simple precursor that can be used as substrate for the synthesis of target molecule. The bonds broken generate molecules called synthons or synthetic equivalent. The latter term is designated to indicate their use as substrate in synthesis. For instance, the synthons generated in phenylacetic acid are given as follows:

  ORGANIC CHEMISTRY (LL)-PACKAGE, Chapter 8.8, Problem 8.21TIY , additional homework tip  1

The best approach to retrosynthetic analysis is to look for easily available reagents such as Grignard reagents.

(b)

Interpretation Introduction

Interpretation: The synthesis of 3,4-dimethyl-3-hexanol from butane should be written.

Concept introduction:Retrosynthetic analysis involves transformation of target molecule into simple precursor that can be used as substrate for the synthesis of target molecule. The bonds broken generate molecules called synthons or synthetic equivalent. The latter term is designated to indicate their use as substrate in synthesis. For instance, the synthons generated in phenylacetic acid are given as follows:

  ORGANIC CHEMISTRY (LL)-PACKAGE, Chapter 8.8, Problem 8.21TIY , additional homework tip  2

The best approach to the retrosynthetic analysis is to look for easily available reagents such as Grignard reagents.

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Redraw the molecule below as a skeletal ("line") structure. Be sure to use wedge and dash bonds if necessary to accurately represent the direction of the bonds to ring substituents. Cl. Br Click and drag to start drawing a structure. : ☐ ☑ P
K m Choose the best reagents to complete the following reaction. L ZI 0 Problem 4 of 11 A 1. NaOH 2. CH3CH2CH2NH2 1. HCI B OH 2. CH3CH2CH2NH2 DII F1 F2 F3 F4 F5 A F6 C CH3CH2CH2NH2 1. SOCl2 D 2. CH3CH2CH2NH2 1. CH3CH2CH2NH2 E 2. SOCl2 Done PrtScn Home End FA FQ 510 * PgUp M Submit PgDn F11
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