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CH(3)-CH(2)-overset(O)overset(||)(C )-OC...

`CH_(3)-CH_(2)-overset(O)overset(||)(C )-OC_(2)H_(5) overset(Naoverset(**)(O)H)underset(H_(2)O^(**))rarr` Products of the above reaction contain

A

`CH_(3)-CH_(2)-overset(O)overset(||)(C )-overset(**)(O^(-))`

B

`CH_(3)-CH_(2)-overset(O^(**))overset(||)(C )-O^(-)`

C

`CH_(3)CH_(2)-overset(**)(O)-H`

D

Both (a) and (b)

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The correct Answer is:
To solve the given reaction, we need to analyze the reactants and the conditions under which the reaction takes place. The reaction involves a compound with a carbonyl group (C=O) and an ether group (–O–C2H5) in the presence of sodium hydroxide (NaOH) and water (H2O). ### Step-by-Step Solution: 1. **Identify the Reactant Structure**: The given compound is CH3-CH2-C(=O)-O-C2H5. This structure consists of a carbon chain (ethyl group) attached to a carbonyl group (C=O) and an ether group (–O–C2H5). 2. **Nucleophilic Attack by Hydroxide Ion**: In the presence of NaOH, the hydroxide ion (OH-) acts as a nucleophile and attacks the carbonyl carbon (C=O). This results in the formation of a tetrahedral intermediate. 3. **Formation of Tetrahedral Intermediate**: The attack of the hydroxide ion leads to the formation of a tetrahedral intermediate where the carbonyl oxygen becomes negatively charged (alkoxide ion). The structure now looks like: CH3-CH2-C(OH)(O-C2H5). 4. **Proton Transfer**: In the next step, there is a proton transfer (H+ transfer) from the hydroxyl group (OH) to the ether oxygen (O-C2H5). This results in the formation of a hydroxyl group and the regeneration of the carbonyl group. 5. **Elimination of Ethanol**: The tetrahedral intermediate collapses, leading to the elimination of ethanol (C2H5OH) as a leaving group. The product formed is: CH3-CH2-C(=O)-OH. 6. **Final Product**: The final product of this reaction is a carboxylic acid (specifically, butanoic acid) and an alkoxide ion (which is the result of the ether group losing a proton). ### Final Products: The products of the reaction are: - Butanoic acid (CH3-CH2-C(=O)-OH) - Ethoxide ion (C2H5O-) ### Summary of Products: The products of the above reaction contain: 1. Butanoic acid (CH3-CH2-C(=O)-OH) 2. Ethoxide ion (C2H5O-)

To solve the given reaction, we need to analyze the reactants and the conditions under which the reaction takes place. The reaction involves a compound with a carbonyl group (C=O) and an ether group (–O–C2H5) in the presence of sodium hydroxide (NaOH) and water (H2O). ### Step-by-Step Solution: 1. **Identify the Reactant Structure**: The given compound is CH3-CH2-C(=O)-O-C2H5. This structure consists of a carbon chain (ethyl group) attached to a carbonyl group (C=O) and an ether group (–O–C2H5). 2. **Nucleophilic Attack by Hydroxide Ion**: ...
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