Using a series of reaction equations, outline how you would synthesize the following compounds from the reactants given. Show all reagents and necessary reaction conditions. You may use any reagents or solvents necessary, but you cannot use starting materials other than those given. a) 2,4-dimethyl-2-pentanol from 4-methylpentene and methyl bromide b) Heptanal from 1-heptene 으 d) -CH,CH,CH,—O-C–CH3 from CH3 Ethylcyclohexane from CH3 -CH₂CH=CH₂ and tert-butyl alcohol -CH₂Br

Using a series of reaction equations, outline how you would synthesize the following compounds from the reactants given. Show all reagents and necessary reaction conditions. You may use any reagents or solvents necessary, but you cannot use starting materials other than those given. a) 2,4-dimethyl-2-pentanol from 4-methylpentene and methyl bromide b) Heptanal from 1-heptene 으 d) -CH,CH,CH,—O-C–CH3 from CH3 Ethylcyclohexane from CH3 -CH₂CH=CH₂ and tert-butyl alcohol -CH₂Br

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter7: Alkynes

Section: Chapter Questions

Problem 7.27P: Following is the structural formula of the tranquilizer meparfynol (Oblivon). Propose a synthesis...

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Concept explainers

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

Using a series of reaction equations, outline how you would synthesize the
following compounds from the reactants given. Show all reagents and necessary
reaction conditions. You may use any reagents or solvents
you
cannot use starting materials other than those given.
necessary, but
a) 2,4-dimethyl-2-pentanol from 4-methylpentene and methyl bromide
b) Heptanal from 1-heptene
c)
d)
CH₂CH₂CH₂
CH2CH2CH2−O–C–CH3
from
CH3
Ethylcyclohexane from
CH3
-CH₂CH=CH₂
and tert-butyl alcohol
aa
CH₂Br

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