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Several additional amine syntheses are effectively limited

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr ISBN: 9780321768414 33

Solution for problem 43SP Chapter 19

Organic Chemistry | 8th Edition

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Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Organic Chemistry | 8th Edition

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Problem 43SP

Several additional amine syntheses are effectively limited to making primary amines. The reduction of azides and nitro compounds and the Gabriel synthesis leave the carbon chain unchanged. Formation and reduction of a nitrile adds one carbon atom. Show how these amine syntheses can be used for the following conversions.

(a) allyl bromide  allylamine

(b) ethylbenzene  p-ethylaniline

(c) 1-bromo-3-phenylheptane  3-phenylheptan-1-amine

(d) 1-bromo-3-phenylheptane  4-phenyloctan-1-amine

Step-by-Step Solution:
Step 1 of 3

q,Co@ + uburla,, L; ge. j*------"t Ch fu tl Dvtn,l,o i $Ue rr'rriJ*)1. -"----{ Cartoon...

Step 2 of 3

Chapter 19, Problem 43SP is Solved
Step 3 of 3

Textbook: Organic Chemistry
Edition: 8
Author: L.G. Wade Jr
ISBN: 9780321768414

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Several additional amine syntheses are effectively limited

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