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chem question organic

Hi, please can i have some help on this question? I initially thought the answer was C but then I realised that oxidative clevage will take place in those conditions. The ms says A but i thought heat was definitely needed for oxidation?
Here is the question: https://ibb.co/HK0FxTQ
Thanks!

Reply 1

Original post by anonymous56754
Hi, please can i have some help on this question? I initially thought the answer was C but then I realised that oxidative clevage will take place in those conditions. The ms says A but i thought heat was definitely needed for oxidation?
Here is the question: https://ibb.co/HK0FxTQ
Thanks!

It’s oxidation of an aldehyde to a carboxylic acid, so you would use acidified K2Cr2O7. You can do the reaction at room temp, but it will proceed slowly compared to when heated.

Reply 2

Original post by TypicalNerd
It’s oxidation of an aldehyde to a carboxylic acid, so you would use acidified K2Cr2O7. You can do the reaction at room temp, but it will proceed slowly compared to when heated.

I see, thanks for clarifying

Reply 3

Original post by anonymous56754
Hi, please can i have some help on this question? I initially thought the answer was C but then I realised that oxidative clevage will take place in those conditions. The ms says A but i thought heat was definitely needed for oxidation?
Here is the question: https://ibb.co/HK0FxTQ
Thanks!

The reaction shown involves the oxidation of an aldehyde group (from the compound on the left) to a carboxylic acid group (in the product on the right). This type of reaction is typically carried out using an oxidizing agent.
Analyzing the options:

Option A: Acidified dichromate (VI) ions

Acidified potassium dichromate (K2Cr2O7K_2Cr_2O_7) is a strong oxidizing agent. It can oxidize aldehydes to carboxylic acids under acidic conditions.

This reagent is suitable for the reaction shown.

Option B: Dilute, acidified manganate (VII) ions

Acidified potassium permanganate (KMnO4KMnO_4) is also a strong oxidizing agent. In its dilute form, it can oxidize aldehydes to carboxylic acids efficiently.

This reagent is also suitable for this reaction.

Option C: Hot, concentrated, acidified manganate (VII) ions

Hot, concentrated KMnO4KMnO_4 is a very strong oxidizing agent that can cause overoxidation or even degrade the compound (e.g., breaking carbon-carbon bonds). This is excessive for the mild oxidation of an aldehyde to a carboxylic acid.

This option is too harsh for the reaction.

Option D: Concentrated sulfuric acid

Concentrated sulfuric acid alone is not an oxidizing agent. It is used for acidifying solutions but does not oxidize aldehydes to carboxylic acids.

This option is incorrect.

Correct Answer:
Both A (acidified dichromate) and B (dilute, acidified manganate) are correct, but the most commonly chosen oxidizing agent for this reaction is A.
HMU on kennetholive51atgmaildotcom

Reply 4

The reaction shown involves the oxidation of an aldehyde group (from the compound on the left) to a carboxylic acid group (in the product on the right). This type of reaction is typically carried out using an oxidizing agent.
Analyzing the options:

Option A: Acidified dichromate (VI) ions

Acidified potassium dichromate (K2Cr2O7K_2Cr_2O_7) is a strong oxidizing agent. It can oxidize aldehydes to carboxylic acids under acidic conditions.

This reagent is suitable for the reaction shown.

Option B: Dilute, acidified manganate (VII) ions

Acidified potassium permanganate (KMnO4KMnO_4) is also a strong oxidizing agent. In its dilute form, it can oxidize aldehydes to carboxylic acids efficiently.

This reagent is also suitable for this reaction.

Option C: Hot, concentrated, acidified manganate (VII) ions

Hot, concentrated KMnO4KMnO_4 is a very strong oxidizing agent that can cause overoxidation or even degrade the compound (e.g., breaking carbon-carbon bonds). This is excessive for the mild oxidation of an aldehyde to a carboxylic acid.

This option is too harsh for the reaction.

Option D: Concentrated sulfuric acid

Concentrated sulfuric acid alone is not an oxidizing agent. It is used for acidifying solutions but does not oxidize aldehydes to carboxylic acids.

This option is incorrect.

Correct Answer:
Both A (acidified dichromate) and B (dilute, acidified manganate) are correct, but the most commonly chosen oxidizing agent for this reaction is A.

Reply 5

Original post by kennetholive
The reaction shown involves the oxidation of an aldehyde group (from the compound on the left) to a carboxylic acid group (in the product on the right). This type of reaction is typically carried out using an oxidizing agent.
Analyzing the options:

Option A: Acidified dichromate (VI) ions

Acidified potassium dichromate (K2Cr2O7K_2Cr_2O_7) is a strong oxidizing agent. It can oxidize aldehydes to carboxylic acids under acidic conditions.

This reagent is suitable for the reaction shown.

Option B: Dilute, acidified manganate (VII) ions

Acidified potassium permanganate (KMnO4KMnO_4) is also a strong oxidizing agent. In its dilute form, it can oxidize aldehydes to carboxylic acids efficiently.

This reagent is also suitable for this reaction.

Option C: Hot, concentrated, acidified manganate (VII) ions

Hot, concentrated KMnO4KMnO_4 is a very strong oxidizing agent that can cause overoxidation or even degrade the compound (e.g., breaking carbon-carbon bonds). This is excessive for the mild oxidation of an aldehyde to a carboxylic acid.

This option is too harsh for the reaction.

Option D: Concentrated sulfuric acid

Concentrated sulfuric acid alone is not an oxidizing agent. It is used for acidifying solutions but does not oxidize aldehydes to carboxylic acids.

This option is incorrect.

Correct Answer:
Both A (acidified dichromate) and B (dilute, acidified manganate) are correct, but the most commonly chosen oxidizing agent for this reaction is A.

B is wrong, because it would oxidise the C=C bond to a diol

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