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What else can I help you with?
Can you explain what halogenation is?
The process of halogenation is a chemical reaction between a compound, usually an organic compound and a halogen. An example of halogenation is fluorination or chlorination.
What is free-radical halogenation of acetic acid?
free-radical halogenation of acetic acid
What is a short note of allylic halogenation?
Halogenation is the result that occurs when a chemical is mixed with a halogen.
Is halogenation typically carried out in a syn or anti fashion?
Halogenation is typically carried out in an anti fashion.
How ethylene can be converted into ethane?
Halogenation
Why direct halogenation of aniline is not possible?
Well, darling, the reason direct halogenation of aniline is a big no-no is because aniline is a strong activating group that will make the halogenation reaction go haywire and give you a messy mixture of products. Plus, the lone pair on the nitrogen atom in aniline will coordinate with the halogenating agent, making it more selective towards other positions on the ring. So, in a nutshell, direct halogenation of aniline is a recipe for disaster in the lab.
Why NaCl is not used for halogenation in Sandmeyer reaction?
because we need hydrogen as well as chlorine in that reaction
Is halogenation of alkanes a nucleophlic or electrophlic mechanism?
alkenes are neutral nucleofiles they undergoes electrophilic addition reactions.
An alkene can be combined with chlorine and bromine in a?
An alkene can undergo halogenation when combined with chlorine or bromine in a halogenation reaction to form a dihalogenated alkane. This reaction involves the addition of a halogen atom across the double bond of the alkene.
Why don't alkanes undergo fluorination?
because halogenation of alkanes with fluorine is very violently exothermic i.e explosive in nature .
What is the mechanism of alpha halogenation in acidic conditions?
In acidic conditions, alpha halogenation involves the substitution of a hydrogen atom with a halogen atom at the alpha position of a carbonyl compound. This reaction is typically catalyzed by an acid, such as hydrochloric acid, and proceeds through the formation of an enol intermediate, which is then attacked by the halogen to form the halogenated product.
What is the halogenation of 3-ethyl-1-pentene with iodine?
When Iodine solid reacts with this alkene in presence of ethanol 1,2-diiodo-3-ethyl penman is produced stereo chemistry of produced compound shows a significant role for determining the properties of product.
