In each case, show how you would synthesize the chloride, bromide, and iodide from the corresponding alcohol.
(a) 1-halobutane bromo, iodo)
(a) Synthesis of 1-halobutane:
Treatment of butan-1-ol with thionyl chloride in the presence of pyridine gives 1-chlorobutane.
Step 2 </p>
Treatment of butan-1-ol with phosphorous tribromide gives 1-bromobutane.
Step 3 </p>
Treatment of butan-1-ol with gives 1-iodobutane.
Step 4 </p>
(b) Synthesis of halocyclopentane:
Treatment of cyclopentanol with thionyl chloride in the presence of pyridine gives chlorocyclopentane.
Step 5 </p>
Treatment of cyclopentanol with phosphorous tribromide gives bromocyclopentane.
Treatment of cyclopentanol with gives iodocyclopentane.
Textbook: Organic Chemistry
Author: L.G. Wade Jr
Organic Chemistry was written by and is associated to the ISBN: 9780321768414. This full solution covers the following key subjects: methylcyclohexane, halo, halocyclopentane, halobutane, chloride. This expansive textbook survival guide covers 25 chapters, and 1336 solutions. The full step-by-step solution to problem: 40SP from chapter: 11 was answered by , our top Chemistry solution expert on 05/06/17, 06:41PM. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. The answer to “In each case, show how you would synthesize the chloride, bromide, and iodide from the corresponding alcohol.(a) 1-halobutane bromo, iodo)(b) halocyclopentane(c) 1-halo-1-methylcyclohexane(d) 1-halo-2-methylcyclohexane” is broken down into a number of easy to follow steps, and 23 words. Since the solution to 40SP from 11 chapter was answered, more than 435 students have viewed the full step-by-step answer.