Bromochlorofluoromethane or fluorochlorobromomethane, is a chemical compound and trihalomethane derivative with the chemical formula CHBrClF. As one of the simplest possible stable chiral compounds, it is useful for fundamental research into this area of chemistry. However, its relative instability to hydrolysis, and lack of suitable functional groups, made separation of the enantiomers of bromochlorofluoromethane especially challenging, and this was not accomplished until almost a century after it was first synthesised, in March 2005, though it has now been done by a variety of methods. More recent research using bromochlorofluoromethane has focused on its potential use for experimental measurement of parity violation, a major unsolved problem in quantum physics. (Wikipedia).
Synthesis of a Bromoalkane (n-Bromopropane)
In this video, I will be making n-bromopropane by brominating 1-propanol. The n-bromopropane can then be used in a Grignard reaction to make butyric acid (smell of vomit). Here is the video of me using it in a Grignard reaction: http://youtu.be/_wmx65zQk58 This process can be used as a
From playlist Syntheses and Demonstrations
Making Bromine From Pool Chlorine Tablets
In this video i am making bromine with TCCA (pool chemical), HCl and NaBr. Support my channel: https://www.patreon.com/chemiolis
From playlist Chemistry for home-labs and self-production
In this video we are making bromine by reacting sodium bromide with chlorine gas. The chlorine gas was produced from TCCA and hydrochloric acid. I am available at other platforms where additional content is uploaded. Make sure to check these out in order not to miss out on something: Ins
From playlist Elements
In this video I make hydrobromic acid from sulfuric acid and sodium bromide. You can also use potassium bromide.
From playlist Syntheses and Demonstrations
The Chemical Elements: The Discovery of Bromine
Bromine, element # 35, was discovered almost simultaneously by two different chemists. Who gets the credit? Chemist: Veena Bidasha Director: Michael Harrison Written and Produced by Kimberly Hatch Harrison Creative Commons Images: Tyrian purple cloth cc Author Boonekamp http://en.wiki
From playlist The Chemical Elements
Make Hydrobromic Acid Revisited 2018
We show how to make hydrobromic acid. Hydrobromic acid is the bromine analogue of hydrochloric acid. While too expensive to use as much as hydrochloric acid, it's often used when the bromine element itself is needed. For example a major use is the synthesis of organobromine compounds like
From playlist Home Science
Making a Strong Oxidizer: Potassium Bromate
In this video we are gong to make potassium bromate which is a strong oxidizing agent. It will be made directly from potassium bromide using an electrolytic cell. Do not try this at home as bromate is toxic and carcinogenic. Patreon: https://www.patreon.com/thyzoid Discord: https://discor
From playlist Organic Chemistry
What Is Thermosetting and Thermosoftening Polymers | Organic Chemistry | Chemistry | FuseSchool
Learn the basics about thermosetting and thermosoftening polymers, when learning about polymers as a part of organic chemistry. A polymer is a macromolecule made of many monomers, or repeating units. The properties of these polymers depend on a variety of factors – the monomer unit, the
From playlist CHEMISTRY
NITRATION TIME! Making A Chemical Called Nitrobromobenzene
In this video we are going to nitrate bromobenzene to make nitrobromobenzene. Patreon: https://www.patreon.com/thyzoid Discord: https://discord.gg/UrjAt44HWH (Let me know if the discord link does not work) Instagram: https://www.instagram.com/thyzoyd/?hl=de 🐦 Twitter: https://twitter.com/
From playlist Organic Chemistry
R,S system | Stereochemistry | Organic chemistry | Khan Academy
How to assign the configuration of a chirality center using the R,S system. Watch the next lesson: https://www.khanacademy.org/science/organic-chemistry/stereochemistry-topic/optical-activity/v/r-s-cahn-ingold-prelog-naming-system-example-2?utm_source=YT&utm_medium=Desc&utm_campaign=organ
From playlist Stereochemistry | Organic Chemistry | Khan Academy
In this video we are making chromyl chloride which is a potent volatile carcinogen. Chromyl chloride (CrO2Cl2) is this red fuming liquid. It can be used to oxidize toluene to benzaldehyde and to oxidize a lot of other reagents. On my instagram and reddit theres plenty of other pictures of
From playlist Inorganic Chemistry