The simplest way would be to make the sodium salt by reacting it with NaOH. Then evaporate it to near dryness and continue heating it with a bunsen burner or similar heat source. The decarboxylation will produce methane. This is hazardous because the methane will catch fire with the flame or any spark so a gas collection apparatus of some sort must be used.
Another method would be to run the electrolysis of the sodium acetate reaction. Methane would be produced at the anode but would be contaminated with CO2 and some ethane. This method is known as the Kolbe electrolysis and is pretty slow.
you can't, it's impossible.
No ethanoic acid is an acid.
Ethanoic acid is vinegar.
Oxidation with acidic KMnO4 or Ozonolysis followed by oxidation
Ethanoic acid (acetic acid) is a weak acid and hydrochloric acid (HCl) is a strong acid. So, ethanoic acid is NOT stronger than hydrochloric acid.
you can't, it's impossible.
you can't, it's impossible.
No ethanoic acid is an acid.
HBr is a strong acid. Ethanoic acid (acetic acid) is a weak acid. So ethanoic acid is weaker.
Ethanoic acid is vinegar.
Oxidation with acidic KMnO4 or Ozonolysis followed by oxidation
Ethanoic acid (acetic acid) is a weak acid and hydrochloric acid (HCl) is a strong acid. So, ethanoic acid is NOT stronger than hydrochloric acid.
you can take NMR of ethanoic acid
Oxalic acid is dicarboxylic acid while ethanoic acid is monocarboxylic acid.
Nothing - vinegar is dilute ethanoic acid.
vinegar is dilute ethanoic acid
Ethanoic acid can donate a proton if there is an accepter in the same solution. Hence, it is a Bronsted-Lowry acid.