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The decreasing order of nucleophilicitie...

The decreasing order of nucleophilicities of the following is :
(I) `H_2 O`
(II) `EtOH`
(III) `MeCOO^(Ө)`
(IV) `overset (Ө) O H`
(V) `EtO^(Ө)`.

A

`(V) gt (IV) gt (III) gt (II) gt (I)`

B

`(I) gt (II) gt (III) gt (IV) gt (V)`

C

`(IV) gt (V) gt (III) gt (II) gt (I)`

D

`(I) gt (II) gt (III) gt (V) gt (IV)`

Text Solution

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The correct Answer is:
To determine the decreasing order of nucleophilicities of the given compounds, we need to analyze their basicity, as nucleophilicity is often correlated with basicity. Here’s the step-by-step solution: ### Step 1: Identify the Compounds The compounds given are: 1. \( H_2O \) (Water) 2. \( EtOH \) (Ethanol) 3. \( MeCOO^- \) (Acetate ion) 4. \( OH^- \) (Hydroxide ion) 5. \( EtO^- \) (Ethoxide ion) ### Step 2: Classify the Compounds - **Anions**: \( MeCOO^- \), \( OH^- \), \( EtO^- \) - **Neutral Molecules**: \( H_2O \), \( EtOH \) ### Step 3: Analyze the Anions Among the anions: - \( EtO^- \) (Ethoxide ion) is a strong base and thus a strong nucleophile due to its negative charge being localized on oxygen. - \( OH^- \) (Hydroxide ion) is also a strong base but less nucleophilic than \( EtO^- \) because it is a smaller alkoxide. - \( MeCOO^- \) (Acetate ion) has resonance stabilization, which delocalizes the negative charge, making it less nucleophilic compared to the other two anions. ### Step 4: Rank the Anions From strongest to weakest nucleophilicity: 1. \( EtO^- \) 2. \( OH^- \) 3. \( MeCOO^- \) ### Step 5: Analyze the Neutral Molecules Among the neutral molecules: - \( H_2O \) is less nucleophilic than \( EtOH \) because ethanol has an ethyl group that can donate electron density, making it a better nucleophile. ### Step 6: Rank the Neutral Molecules From strongest to weakest nucleophilicity: 1. \( EtOH \) 2. \( H_2O \) ### Step 7: Combine the Rankings Now, combining the rankings from both anions and neutral molecules, we get the overall decreasing order of nucleophilicity: 1. \( EtO^- \) (Ethoxide ion) 2. \( OH^- \) (Hydroxide ion) 3. \( MeCOO^- \) (Acetate ion) 4. \( EtOH \) (Ethanol) 5. \( H_2O \) (Water) ### Final Order Thus, the final decreasing order of nucleophilicities is: \[ EtO^- > OH^- > MeCOO^- > EtOH > H_2O \] ---

To determine the decreasing order of nucleophilicities of the given compounds, we need to analyze their basicity, as nucleophilicity is often correlated with basicity. Here’s the step-by-step solution: ### Step 1: Identify the Compounds The compounds given are: 1. \( H_2O \) (Water) 2. \( EtOH \) (Ethanol) 3. \( MeCOO^- \) (Acetate ion) 4. \( OH^- \) (Hydroxide ion) ...
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