Chloroform

You cannot prepare chloroform at home. Chloroform is prepared by heating a mixture of chlorine and either chloromethane or methane. In turn putting out 3 separate chemical reactions. After that, it undergoes another does of chlorination. The output of this process is a mixture of the four chloromethanes: chloromethane, dichloromethane, chloroform (trichloromethane), and carbon tetrachloride, which are then separated by distillation.

So unless you have these kinds of chlorine just laying around, you might just wanna buy some chloroform (which would be almost impossible because it's hard to prove a legitimate claim to use it). Remember that it is illegal to use it for uses not mentioned (ie don't drug women with it)

-Brett

The time it takes for a person to pass out after being exposed to chloroform can vary depending on factors such as the person's weight, health status, and the concentration of chloroform in the air. Typically, it can take anywhere from a few seconds to a couple of minutes for someone to lose consciousness when exposed to chloroform.

Using the ideal gas law, we can determine that the molar mass of chloroform is approximately 119 g/mol. Given the pressure, temperature, and density of chloroform, you can calculate the molar mass using the formula: (pressure x molar mass) / (gas constant x temperature) = density. Solving for molar mass gives approximately 119 g/mol.

Chloroform is a controlled substance and should only be obtained by licensed professionals for specific approved uses, like in research or medical settings. Unauthorized use or handling of chloroform can be dangerous and illegal.

To prepare chloroform water, mix chloroform with water in the desired ratio. It's important to handle chloroform with proper safety measures, such as working in a well-ventilated area, wearing gloves, and following appropriate disposal protocols for chloroform waste.

Chloroform is commonly found in some industrial solvents, household products like paint strippers and adhesives, and as a byproduct in water treatment processes. It is also used in the production of some plastics, medications, and pesticides.

Chloroform is not typically used as a preservative for organisms. It is a solvent that has been historically used for anesthesia and as a reagent in laboratory settings, but it is toxic and poses health risks. Other safer methods, such as formalin or ethanol, are generally preferred for preserving organisms.

polar molecules are water soluble , non-polar molecules are fat soluble . Chloroform (as are most anesthetics) is more soluble in fats (the cell membrane) than in water (ie.blood).

Thus it is classified as non-polar notwithstanding the data below.

Chloroform is a polar molecule. The 3 chlorine atoms are considerably more electronegative than the hydrogen atom, so the molecule has a net dipole moment.

Yes, chloroform is less volatile than water because it has a higher boiling point, meaning it evaporates more slowly at room temperature.

Everything can make someone unconscious if administered in the wrong way. Even something that is considered by most people as safe- such as drinking water. Although, nothing is a poison without a dosage. Some common chemicals that were used to make people unconscious were chloroform and diethyl ether. Chloroform can be made simply with bleach and acetone. But remember it is dangerous to use without the known dosage and there may be some toxic ingredients that will spawn from the mixture such as chlorine.

The molecular formula for chloroform is CHCl3.

Chloroform is a hazardous chemical that should not be used for self-administered purposes. Its use is strictly regulated due to its toxic and potentially lethal effects on the body. If medical professionals determine chloroform is necessary for a procedure, they will have the expertise to safely administer it in a controlled environment. It should never be used without proper training and guidance.

i wouldn't recommend it, that's rape! lol

-------------------

Taken from a different question...

It could, but technically it's a pretty bad idea. For one thing, unless she agrees to letting you do it, that would be considered assault and rape. For another thing, inappropriate use of substances such as chloroform is extremely dangerous and very illegal. The hazards of using chloroform to knock someone out could cause a range of injuries, such as smashing their head if you fail to catch them when they fall out, cutting off their oxygen or creating some other life-threatening symptom due to a disorder or disease, like asthma or something, and can even cause sudden sniffer's death, which is basically unexpected cardiac arrest.

So basically, you could use it, but I really wouldn't recommend it unless you want to go to jail.

Chloroform has a lower boiling point than water, so it evaporates more quickly when applied to the skin, causing a cooling sensation. This rapid evaporation absorbs heat from the skin, making it feel colder than water, which evaporates more slowly. Additionally, chloroform has a lower specific heat capacity than water, meaning it requires less energy to change its temperature, contributing to the perception of coldness.

Chloroform is a compound made up of one carbon atom, one hydrogen atom, and three chlorine atoms, with the chemical formula CHCl3. It is a colorless, sweet-smelling liquid commonly used as a solvent in laboratories and in industry.

No, chloroform is a colorless liquid with a slightly sweet odor.

Shaking bromine water with chloroform is a common test to detect the presence of unsaturation in a compound. If an alkene is present, it will react with bromine to decolorize the bromine water, forming a colorless solution due to the addition of bromine across the double bond. This test is known as the bromine test for unsaturation.

Dr. James Simpson did not invent chloroform; it was actually discovered independently by American physician Samuel Guthrie and French chemist Eugène Soubeiran in 1831. Dr. Simpson was renowned for popularizing the use of chloroform as an anesthetic during childbirth in the mid-19th century.

Chloroform abuse can lead to serious health risks such as respiratory depression, liver and kidney damage, and central nervous system depression. Overexposure to chloroform can result in dizziness, nausea, headaches, and in extreme cases, unconsciousness or death. Long-term abuse can also lead to addiction and dependence.

Chloroform was historically used as an anesthetic but is no longer used in that manner due to its toxicity. It is now mainly used as a solvent in laboratories for various purposes, such as extracting organic compounds. It is important to handle chloroform with caution due to its health hazards.

Cell membranes are composed of a lipid bilayer, which is impermeable to water-soluble substances but allows fat-soluble substances to easily pass through. Fat-soluble substances like chloroform and ether can dissolve in the lipid bilayer of the cell membrane and penetrate cells rapidly, leading to their rapid effects on cells.

This is because in the presence of air chloroform is oxidised to phosgene. To prevent the formation of phosgene, they are stored in dark colored bottles.
CHCl3 + 1/2 O2 ---->HCl + COCl2.

Phosgene is represented as COCl2. This is poisonous.

chloroform is more polar than hexane. Based from the solvent polarity chart, alkyl halides (such as CHCl3) are relatively more polar than alkanes (such as hexane). Moreso, alkanes tend to be the least polar among the organic and inorganic compounds due to their hydrocarbon structure.

Chloroform is used in DNA extraction to separate DNA from proteins and lipids. It helps to denature and precipitate the proteins and disrupt the cell membranes to release the DNA. The DNA can then be further purified and isolated for downstream applications.

Chloroform is used in DNA isolation to separate the DNA from other cellular components like proteins and lipids. It helps in the denaturation of proteins, disrupting their structure and allowing the DNA to separate into the aqueous phase. Chloroform aids in the extraction and purification of DNA from the sample.