One hydrazine reacts with two acetone to yield two 2-propanol and one nitrogen (gas).
Benzyl chloride reacts faster than 1-chlorobutane with sodium iodide in acetone due to the stability of the benzylic carbocation intermediate formed in the reaction, which facilitates nucleophilic attack by iodide. The resonance stabilization of the benzyl carbocation makes it more reactive compared to the primary alkyl carbocation formed in the case of 1-chlorobutane.
Potassium dichromate is orange and when it reacts with ethanol which is a primary alcohol it is going to oxidise it to form aldehyde which is colorless. so the color change is from Orange to Colorless. :)
Ethanol requires oxygen to burn. During the combustion process, ethanol reacts with oxygen to produce carbon dioxide, water, and heat.
A salt and water is formed in this type of reactions.
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The product formed when benzoic acid reacts with ethanol is ethyl benzoate, along with water. This reaction is an esterification process, where the -OH group of the benzoic acid reacts with the -OH group of ethanol to form the ester and water as a byproduct.
No, because when you add acetone to acetone, all you are doing is adding more of the volume of acetone to acetone. You are just changing the amount of acetone, not anything chemically happening.
Ethyl formate is formed when ethanol reacts with formic acid. This reaction is an esterification reaction where the hydroxyl group of ethanol reacts with the carboxyl group of formic acid to form the ester.
When an alcohol reacts with sodium metal, a salt called sodium alkoxide is formed along with hydrogen gas. This process is known as alcohol deprotonation or alkoxide formation.
The reaction of acetone with Triiodomethane is a nucleophilic addition reaction. It forms a yellow-orange precipitate, due to the formation of the iodoform compound.
Metallic sodium reacts vigorously with ethanol to form sodium ethanoate.
The reaction of cinnamaldehyde and acetone typically results in the formation of 2'-Hydroxychalcone, also known as butein. Butein is a natural chalcone derivative that has been studied for its various biological activities, including antioxidant and anti-inflammatory properties.
When ethanol reacts with bromine water, the bromine is displaced by the oxygen in ethanol, resulting in decolorization of the bromine water. This reaction occurs because ethanol is a reducing agent, which means it can donate electrons to the bromine atoms, converting them from a colored form (brown/red) to a colorless form.
Acetone can react with Grignard reagents to form alcohols, which can hinder the desired reaction. Additionally, acetone can also quench Grignard reagents by reacting with them before they can react with the desired substrate. Therefore, acetone is not an ideal solvent for reactions involving Grignard reagents.
Potassium dichromate is orange and when it reacts with ethanol which is a primary alcohol it is going to oxidise it to form aldehyde which is colorless. so the color change is from Orange to Colorless. :)
When sulfur reacts with a metal, a metal sulfide salt is usually formed.
Purple colour