Embibe Experts Solutions for Chapter: Organic Nitrogen Compounds, Exercise 1: Exercise
Embibe Experts Chemistry Solutions for Exercise - Embibe Experts Solutions for Chapter: Organic Nitrogen Compounds, Exercise 1: Exercise
Attempt the free practice questions on Chapter 13: Organic Nitrogen Compounds, Exercise 1: Exercise with hints and solutions to strengthen your understanding. Chemistry Crash Course (Based on Revised Syllabus-2023) solutions are prepared by Experienced Embibe Experts.
Questions from Embibe Experts Solutions for Chapter: Organic Nitrogen Compounds, Exercise 1: Exercise with Hints & Solutions
Write down the structure and IUPAC names of all isomeric nitro compounds having molecular formula .

Name the product formed by the electrolytic reduction of nitro methane.

Write the equation for the sulphonation of nitrobenzene.

Write the reaction for the acidic hydrolysis of ethanenitrile.

How do you make the chlorophenylmethane to phenylacetic acid conversion?

Write the equations involved in the conversion of acetamide and propanaldehydeoxime to methyl cyanide and ethyl cyanide respectively.

Haloalkanes react with to form alkyl cyanides as main product while forms isocyanides as the chief product. Explain.

Identify the product formed, when ethyl chloride is heated with .
