Why is chloroform a good solvent

In the s, chloroform was used during the birth of Queen Victoria's last two children. Explain it with Molecules. How do Drugs Work? Toggle navigation World of Molecules. Chloroform Molecule. Justus von Liebig carried out the alkaline cleavage of chloral. In , Scottish obstetrician James Y.

Simpson was the first to demonstrate the anaesthetic properties of chloroform on humans and helped to popularise the drug for use in medicine. By the s, chloroform was being produced on a commercial basis by using the Liebig procedure, which retained its importance until the s.

Download it here: J J Shephard et al , Chem. Topics Atoms and bonds Matter. Related articles. Research Telescope arrangement puts a twist on organic synthesis TZ Solvents, move aside — scientists achieve dry multicomponent synthesis in a single step with twisting screws.

Load more articles. No comments yet. You're not signed in. To link your comment to your profile, sign in now. Only registered users can comment on this article. Hexane, on the other end of the polarity scale, extracts polar solutes very poorly.

Thus, chloroform and ethyl ether are the most versatile solvents, although dichloromethane and 1-chlorobutane are finding more use. Solvent costs and health hazards vary within the group of solvents discussed. While chloroform has the lowest TLV, a safety limit, some of the other solvents have higher vapor pressures.