•  
  •  
 

Document Type

Research

Abstract

When the carbonyl group is joined directly to carbon and hydrogen (aldehydic) or to carbon and carbon (ketonic) it reacts with phenylhydrazine to give the corresponding phenylhydrazone. When the radical is joined directly to nitrogen and hydrogen, as in formanilide, the products are aniline and formylphenylhydrazine. Substitution productions of formanilide behave similarly. If the radical is joined directly to nitrogen and nitrogen, as in diphenylurea, the products are aniline and a semicarbazide. The corresponding thiourea behaves similarly, and gives a thiosemicarbazide. If the reaction with the thioureas is carried out in the presence of a desulphurizing agent, guanidine derivatives are obtained.

Publication Date

1931

Journal Title

Proceedings of the Iowa Academy of Science

Volume

38

Issue

1

First Page

171

Last Page

171

Copyright

© Copyright 1931 by the Iowa Academy of Science, Inc.

Language

EN

File Format

application/pdf

Share

COinS
 
 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.