How will you convert ethene to ethanoic acid?

Answer: Ethane can be converted to ethanoic acid or acetic acid by catalytic oxidation. There are a number of ways, depending upon the catalyst, to achieve this conversion. The commonly used catalysts for this conversion include, protonated pentasil-type zeolite (or, H-ZSM-5), Fe/ZSM-5, , etc.

How will we convert ethene to ethane?

This process is called catalytic hydrogenation as it involves a catalyst to drive the reaction and produces alkanes as a product. In the given scenario, as ethene ( ) is an alkene, it can be converted into ethane by catalytic hydrogenation or Addition of hydrogen.

How do you make ethanoic acid from propanoic acid?

To convert propanoic acid to ethanoic acid (the number of carbon atoms are decreasing), we need propionamide (amide group-RCONH2). Then propionamide undergoes Hoffman Bromamide reaction to form methylamine. Then methylamine formed can be converted to ethanol to form ethanoic acid by oxidation.

How do you convert ethane to propanoic acid?

Step-1:-Chlorination of ethane. Ethane is treated with chlorine to form ethyl chloride. Step-2:-Conversion of ethyl chloride into propanoic acid. Ethyl chloride on reaction with alcoholic KCN gives ethyl cyanide, which on hydrolysis gives propanoic acid.

What is the conversion of ethene to propene?

The selective and stable conversion of ethene to propene,3 C2H4 — 2C3H6, was found on Ni-loaded mesoporous silica catalysts in a continuous gas-flow system at around 673 K and atmospheric pressure.

How can I convert propanoic acid to ethyl bromide?

Step1- convert propanoic acid to propanamide by treating the latter with ammonia. Step3 – convert ethanamine to ethanoic acid by acid hydrolysis. Step4- convert ethanoic acid to ethanol by reducing latter using lithium aluminum hydride. Step5- convert ethanol to ethyl bromide by treating latter with HBr . There are many ways other than this.

How can I convert propanol to butanoic acid?

Treat propanol (I am assuming 1-propanol, even though you don’t specify) with HCl or thionyl chloride to form 1-chloropropane. Then Grignard reaction with C O2. Convert the alcohol to a better leaving group, using, e.g., p-TsCl. Then react with Na C N to form butanenitrile. Then acid- or base-catalyzed hydrolysis to butanoic acid.

https://www.youtube.com/watch?v=9_z9Kto4F_8