Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Chapter 12, Problem 25P

Show how 1-pentanol could be transformed into each of the following compounds. (You may use any needed inorganic reagents and you need not show the synthesis of a particular compound more than once.)

(a) 1-Bromopentane

(b) 1-Pentene

(c) 2-Pentanol

(d) Pentane

(e) 2-Bromopentane

(f) 1-Hexanol

(g) 1-Heptanol

(h) Pentanal

(i) 2-Pentanone

(j) Pentanoic acid

(k) Dipentyl ether (two ways)

(l) 1-Pentyne

(m) 2-Bromo-1-pentene

(n) Pentyllithium

(o) 4-Methyl-4-nonanol

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Students have asked these similar questions
How could you convert each of the following compounds into butanoic acid? Write each step showing all reagents. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene
Show how you would synthesize the following compounds, starting with acetylene and any compounds containing nomore than four carbon atoms.(a) hex-1-yne (b) hex-2-yne(c) cis-hex-2-ene (d) trans-hex-2-ene
Develop syntheses for the following compounds. As starting materials, you may use cyclopentanol, alcohols containing no more than four carbon atoms, and any common reagents and solvents. (a) trans-cyclopentane-1,2-diol (b) 1-chloro-1-ethylcyclopentane

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