Solution Found!

The two most general amine syntheses are the reductive

Chapter 13, Problem 42SP

(choose chapter or problem)

Get Unlimited Answers
QUESTION:

The two most general amine syntheses are the reductive amination of carbonyl compounds and the reduction of amides. Show how these techniques can be used to accomplish the following syntheses.

(a) benzoic acid  benzylamine

(b) benzaldehyde  benzylamine

(c) pyrrolidine  -ethylpyrrolidine

(d) cyclohexanone  -cyclohexylpyrrolidine

(e) \(\mathrm{HOOC}-\left(\mathrm{CH}_{2}\right)_{3}-\mathrm{COOH} \rightarrow\) pentane- 1,5 -diamine (cadaverine)

Equation transcription:

Text transcription:

{HOOC}-({CH}{2}){3}-{COOH} rightarrow

Questions & Answers

QUESTION:

The two most general amine syntheses are the reductive amination of carbonyl compounds and the reduction of amides. Show how these techniques can be used to accomplish the following syntheses.

(a) benzoic acid  benzylamine

(b) benzaldehyde  benzylamine

(c) pyrrolidine  -ethylpyrrolidine

(d) cyclohexanone  -cyclohexylpyrrolidine

(e) \(\mathrm{HOOC}-\left(\mathrm{CH}_{2}\right)_{3}-\mathrm{COOH} \rightarrow\) pentane- 1,5 -diamine (cadaverine)

Equation transcription:

Text transcription:

{HOOC}-({CH}{2}){3}-{COOH} rightarrow

ANSWER:

Solution 42SP

(a)        The conversion of reactant into product is given below -

(b)        The conversion of reactant into product is given below -

Add to cart


Study Tools You Might Need

Not The Solution You Need? Search for Your Answer Here:

×

Login

Login or Sign up for access to all of our study tools and educational content!

Forgot password?
Register Now

×

Register

Sign up for access to all content on our site!

Or login if you already have an account

×

Reset password

If you have an active account we’ll send you an e-mail for password recovery

Or login if you have your password back