Oxidation reaction from alcohol to aldehyde

In summary, oxidation reactions from primary alcohols to aldehydes/carboxylic acids or secondary alcohols to ketones require an acid (positive hydrogen ion) because the oxidizing agent, MnO4, needs a source of protons in order to be reduced and cause the oxidation reaction. This is because the half reaction of MnO4 requires low pH to be effective.
  • #1
kathyt.25
49
0
My original question:
Why do oxidation reactions from primary alcohols to aldehydyes/carboxylic acids, or secondary alcohols to ketones require an acid (positive hydrogen ion)? I can see that the reason we have an oxidizing agent is to take away two hydrogen ions from the alcohol, but
why do we need an additional positive hydrogen ion?

Someone's response:
You need a strong electrolytic solution to facilitate the transition
(movement) of electrons... because in order for MnO4 to be reduced
(and cause an oxidation), it needs a source of protons as part of the
chemistry.


Can someone explain WHY we need protons in order for the oxidizing agent to be reduced, and therefore oxidize the alcohol?
If an alcohol is being oxidized to become an aldehyde, it's losing two hydrogen atoms, which are positive... why would these positive hydrogen atoms (protons) be drawn to the source of protons?
 
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  • #2
It has nothing to do with alcohol/aldehyde. MnO4- half reaction is

MnO4- + 8H+ -> Mn2+ + 4H2O + 5e-

To be an effective oxidizer it requires low pH.
 
  • #3


I can explain the role of protons in the oxidation reaction from alcohol to aldehyde. In this reaction, the oxidizing agent (such as MnO4) is reduced, meaning it gains electrons. In order for this to happen, there needs to be a source of protons present. This is because protons act as a positive charge carrier, which helps facilitate the movement of electrons from the alcohol to the oxidizing agent.

In the case of primary alcohols, the alcohol molecule loses two hydrogen atoms, which are then taken up by the oxidizing agent. These hydrogen atoms are positively charged, and are attracted to the source of protons (the acid) in the reaction mixture. This attraction helps to facilitate the transfer of electrons from the alcohol to the oxidizing agent, allowing for the oxidation reaction to occur.

In summary, the presence of protons (positive hydrogen ions) is necessary for the reduction of the oxidizing agent, which in turn allows for the oxidation of the alcohol to occur. Without a source of protons, the electrons cannot be transferred and the reaction cannot take place.
 

1. What is an oxidation reaction from alcohol to aldehyde?

An oxidation reaction from alcohol to aldehyde is a chemical process in which an alcohol molecule loses hydrogen atoms and gains oxygen atoms, resulting in the formation of an aldehyde molecule.

2. How does an oxidation reaction from alcohol to aldehyde occur?

The oxidation reaction from alcohol to aldehyde occurs through the breaking of a carbon-hydrogen bond in the alcohol molecule, followed by the addition of an oxygen atom to the carbon atom, resulting in the formation of an aldehyde molecule.

3. What are the products of an oxidation reaction from alcohol to aldehyde?

The products of an oxidation reaction from alcohol to aldehyde are an aldehyde molecule and a reduced form of an oxidizing agent, such as a metal ion or an organic compound.

4. What is the purpose of an oxidation reaction from alcohol to aldehyde?

The purpose of an oxidation reaction from alcohol to aldehyde is to convert an alcohol molecule into an aldehyde molecule, which can be used as a precursor for the synthesis of various organic compounds in industries such as pharmaceuticals, perfumes, and plastics.

5. What factors can influence the rate of an oxidation reaction from alcohol to aldehyde?

The rate of an oxidation reaction from alcohol to aldehyde can be influenced by factors such as the type of alcohol, the strength of the oxidizing agent, temperature, and the presence of catalysts or inhibitors.

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