Amines

Get insights from 163 questions on Amines, answered by students, alumni, and experts. You may also ask and answer any question you like about Amines

Follow Ask Question
163

Questions

0

Discussions

5

Active Users

0

Followers

New answer posted

a month ago

0 Follower 1 View

V
Vishal Baghel

Contributor-Level 10

Kjeldahl's method does not work for heterocyclic and azo compounds.

New answer posted

a month ago

0 Follower 2 Views

V
Vishal Baghel

Contributor-Level 10

Aliphatic diazonium salts are not stable. Aromatic diazonium salts exist at low temp of 0 – 4°C.

New answer posted

a month ago

0 Follower 2 Views

R
Raj Pandey

Contributor-Level 9

R-CONH? + Br? + 4NaOH → R-NH? + 2NaBr + Na? CO? + 2H? O
This reaction is the Hoffmann bromamide degradation, in which an amide is converted to a 1° amine.

New answer posted

a month ago

0 Follower 1 View

R
Raj Pandey

Contributor-Level 9

Kindly consider the following Image 

 

New answer posted

a month ago

0 Follower 2 Views

A
alok kumar singh

Contributor-Level 10

In diacetamide (CH? CO)? NH), the lone pair of electrons on the nitrogen atom is delocalized through resonance with both adjacent carbonyl groups. This extensive resonance greatly decreases the electron density on the nitrogen atom.

New answer posted

a month ago

0 Follower 1 View

R
Raj Pandey

Contributor-Level 9

Only 1° amine react with benzene sulphonyl chloride to give a compound which is soluble in alkali

 

New answer posted

a month ago

0 Follower 1 View

A
alok kumar singh

Contributor-Level 10

In the ammonolysis reaction, HCl is produced as a byproduct. To neutralize this acidic impurity, the mixture is treated with NaOH.

New answer posted

a month ago

0 Follower 2 Views

R
Raj Pandey

Contributor-Level 9

In Hoffmann bromamide reaction, hypobromite ion react with amide and in this reaction carbonyl group is lost as CO? ²? in form of Na? CO?

New answer posted

a month ago

0 Follower 1 View

V
Vishal Baghel

Contributor-Level 10

In the ammonolysis process, bond cleavage is carried out in the presence of NH? When a halide compound is treated with NH? , the halide ion (X? ) is substituted by an amino group (NH? ) in a nucleophilic substitution reaction.

New answer posted

a month ago

0 Follower 2 Views

V
Vishal Baghel

Contributor-Level 10

Kindly consider the following figure

Get authentic answers from experts, students and alumni that you won't find anywhere else

Sign Up on Shiksha

On Shiksha, get access to

  • 65k Colleges
  • 1.2k Exams
  • 686k Reviews
  • 1800k Answers

Share Your College Life Experience

×

This website uses Cookies and related technologies for the site to function correctly and securely, improve & personalise your browsing experience, analyse traffic, and support our marketing efforts and serve the Core Purpose. By continuing to browse the site, you agree to Privacy Policy and Cookie Policy.