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Xunderset((ii)H3O^(o+))overset((i)KMnO4/...

`Xunderset((ii)H_3O^(o+))overset((i)KMnO_4//H_2O // Delta)toHOOC-oversetoverset(O)(||)C-CH_2-CH_2-CH_2-CH_2-COOH`
X may be

A

B

C

D

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To solve the question, we need to determine the compound X that, when treated with potassium permanganate (KMnO4) in the presence of water and heat, leads to the formation of a specific dicarboxylic acid. ### Step-by-Step Solution: 1. **Identify the Product**: The product given is a dicarboxylic acid with the structure HOOC-CO-CH2-CH2-CH2-CH2-COOH. This indicates that there are two carboxylic acid groups (-COOH) at the ends of a carbon chain. 2. **Understand the Reagents**: The reagent used is potassium permanganate (KMnO4), which is a strong oxidizing agent. It can oxidize alkenes to form diols and further oxidize them to carboxylic acids. 3. **Determine the Structure of X**: Since KMnO4 will oxidize an alkene, we need to consider that X must be a compound that can yield the dicarboxylic acid upon oxidation. The presence of two -COOH groups suggests that X should be a compound with a double bond that can be cleaved to form these groups. 4. **Consider Possible Structures for X**: - A reasonable candidate for X is a compound that has a double bond between two carbon atoms, with sufficient carbon atoms on either side to allow for the formation of the dicarboxylic acid. - A suitable structure could be a compound like 1,5-hexadiene, which has a double bond between the first and second carbon atoms. 5. **Oxidation Mechanism**: When 1,5-hexadiene is treated with KMnO4: - The double bond will be oxidized to form a glycol (diol). - Further oxidation will cleave the carbon-carbon bond, leading to the formation of two carboxylic acid groups at the ends of the carbon chain. 6. **Final Structure Confirmation**: After the oxidation and hydrolysis, the resulting structure matches the dicarboxylic acid given in the question. 7. **Conclusion**: Therefore, the compound X is likely to be 1,5-hexadiene or a similar alkene that can yield the specified dicarboxylic acid upon oxidation with KMnO4.

To solve the question, we need to determine the compound X that, when treated with potassium permanganate (KMnO4) in the presence of water and heat, leads to the formation of a specific dicarboxylic acid. ### Step-by-Step Solution: 1. **Identify the Product**: The product given is a dicarboxylic acid with the structure HOOC-CO-CH2-CH2-CH2-CH2-COOH. This indicates that there are two carboxylic acid groups (-COOH) at the ends of a carbon chain. 2. **Understand the Reagents**: The reagent used is potassium permanganate (KMnO4), which is a strong oxidizing agent. It can oxidize alkenes to form diols and further oxidize them to carboxylic acids. ...
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