Halogenation of methane in direct sunlight, does not produce the compound:
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Answer:
Explanation:
If a mixture of methane and chlorine is exposed to a flame, it explodes - producing carbon and hydrogen chloride. This is not a very useful reaction! The reaction we are going to explore is a more gentle one between methane and chlorine in the presence of ultraviolet light - typically sunlight. This is a good example of a photochemical reaction - a reaction brought about by light.
CH4+Cl2+energy→CH3Cl+HCl(3.4.2)
The organic product is chloromethane. One of the hydrogen atoms in the methane has been replaced by a chlorine atom, so this is a substitution reaction. However, the reaction doesn't stop there, and all the hydrogens in the methane can in turn be replaced by chlorine atoms.
Substitution reactions happen in which hydrogen atoms in the methane are replaced one at a time by chlorine atoms. You end up with a mixture of chloromethane, dichloromethane, trichloromethane and tetrachloromethane.
The original mixture of a colorless and a green gas would produce steamy fumes of hydrogen chloride and a mist of organic liquids. All of the organic products are liquid at room temperature with the exception of the chloromethane which is a gas.
If you were using bromine, you could either mix methane with bromine vapor, or bubble the methane through liquid bromine - in either case, exposed to UV light. The original mixture of gases would, of course, be red-brown rather than green.
You wouldn't choose to use these reactions as a means of preparing these organic compounds in the lab because the mixture of products would be too tedious to separate. The mechanisms for the reactions are explained on separate pages.
Alkanes (the most basic of all organic compounds) undergo very few reactions. One of these reactions is halogenation, or the substitution of a single hydrogen on the alkane for a single halogen to form a haloalkane. This reaction is very important in organic chemistry because it opens a gateway to further chemical reactions.
Halogenation Reaction
While the reactions possible with alkanes are few, there are many reactions that involve haloalkanes. In order to better understand the mechanism (a detailed look at the step by step process through which a reaction occurs), we will closely examine the chlorination of methane. When methane (CH4) and chlorine (Cl2) are mixed together in the absence of light at room temperature nothing happens. However, if the conditions are changed, so that either the reaction is taking place at high temperatures (denoted by Δ) or there is ultra violet irradiation, a product is formed, chloromethane (CH3Cl).
Answer:
A
Explanation: