×
Log in to StudySoup
Get Full Access to Organic Chemistry - 8 Edition - Chapter 19 - Problem 43sp
Join StudySoup for FREE
Get Full Access to Organic Chemistry - 8 Edition - Chapter 19 - Problem 43sp

Already have an account? Login here
×
Reset your password

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

  • Textbook Solutions
  • 2901 Step-by-step solutions solved by professors and subject experts
  • Get 24/7 help from StudySoup virtual teaching assistants
Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Organic Chemistry | 8th Edition

4 5 1 301 Reviews
12
0
Problem 43SP

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 rkre b.cl0Fovne oQ 6,olo3^co.[ I l"\oks.r\gs, Ir -*tt \iving ofgar4lsvllaga'

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

Other solutions

People also purchased

Related chapters

Unlock Textbook Solution

Enter your email below to unlock your verified solution to:

Several additional amine syntheses are effectively limited