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What is formed with ethanol and cinnamic acid?
When ethanol reacts with cinnamic acid in the presence of a catalyst, it forms ethyl cinnamate, which is a commonly used flavoring and fragrance compound. It has a sweet, fruity odor similar to that of strawberries.
Why benzyl chloride reacts faster than 1-clorobutane when treated with sodium iodide in acetone?
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.
What gas is required for ethanol to burn?
Ethanol requires oxygen to burn. During the combustion process, ethanol reacts with oxygen to produce carbon dioxide, water, and heat.
What is the CO2 reaction with hydrazine hydrate?
When CO2 reacts with hydrazine hydrate, it forms hydrazine, water, and carbon dioxide. This reaction is typically carried out in the presence of a catalyst and under controlled conditions to ensure the desired products are obtained. Hydrazine is a key ingredient in rocket propellants and is also used in various industrial processes.
What colour change will occur when potassium dichromate reacts with ethanol?
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 ethanol reacts with oxygen what product is formed?
When ethanol reacts with oxygen, carbon dioxide and water are produced. This reaction typically occurs during combustion, such as burning ethanol as fuel.
What ester is formed when ethanol reacts with formic acid?
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.
What is the product formed when benzoic acid reacts with ethanol?
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.
How do you convert aniline into phenyl hydrazine?
Aniline can be converted into phenyl hydrazine by reacting it with hydrazine hydrate in the presence of an acid catalyst such as hydrochloric acid. The reaction proceeds through the formation of a diazonium salt intermediate, which then reacts with excess hydrazine to form phenyl hydrazine.
Does acetone reacts with acetone?
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.
What are the two compounds formed between PCl5 and ethanol?
The two compounds formed between PCl5 and ethanol are ethyl chloride (C2H5Cl) and diethyl ether (C4H10O). Ethyl chloride is produced when one mole of PCl5 reacts with one mole of ethanol, while diethyl ether is formed when two moles of ethanol react with one mole of PCl5.
What is formed with ethanol and cinnamic acid?
When ethanol reacts with cinnamic acid in the presence of a catalyst, it forms ethyl cinnamate, which is a commonly used flavoring and fragrance compound. It has a sweet, fruity odor similar to that of strawberries.
What gas is evolved when acetone-bisulfite with HCl?
When acetone bisulfite reacts with HCl, sulfur dioxide gas is evolved.
What type of product is formed on reaction of an alcohol with Na metal?
when sodium react with ethanol ,ethoxide and hydrogen are formed. this reaction is like when sodium reacts with water
Is sodium soluble in ethanol?
Metallic sodium reacts vigorously with ethanol to form sodium ethanoate.
Why benzyl chloride reacts faster than 1-clorobutane when treated with sodium iodide in acetone?
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.
What is formed when Ethene reacts with steam?
Ethanol only.
