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So it's late and I just want to be done with this homework packet so here's my prob.
CH3CH2OH ----> -----> Ethane
So there's an intermediate reaction, starting with ethanol, which is a first degree alcohol so I don't think redox is involved since it'd evolve to an aldehyde and then a carboxylic acid, which obviously isn't the product since it's an alkane.
Reverse engineering the problem, I can obviously make an alkane from an alkene, and an alkene can undergo a hydration reaction to become an alcohol. I'd assume an alcohol can have HOH stripped from it in turn to create an alkene which can then be hydrogenated with H2 to create an alkane. So I'm guessing the answer is:
Pt, Ni, or Pd (as a metal catalyst for the hydration reaction in the middle)
CH3CH2OH - HOH -----> CH3=CH2 + H2 --------------> Ethane
What do you guys think?
CH3CH2OH ----> -----> Ethane
So there's an intermediate reaction, starting with ethanol, which is a first degree alcohol so I don't think redox is involved since it'd evolve to an aldehyde and then a carboxylic acid, which obviously isn't the product since it's an alkane.
Reverse engineering the problem, I can obviously make an alkane from an alkene, and an alkene can undergo a hydration reaction to become an alcohol. I'd assume an alcohol can have HOH stripped from it in turn to create an alkene which can then be hydrogenated with H2 to create an alkane. So I'm guessing the answer is:
Pt, Ni, or Pd (as a metal catalyst for the hydration reaction in the middle)
CH3CH2OH - HOH -----> CH3=CH2 + H2 --------------> Ethane
What do you guys think?