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Which is most reactive in base cataysed ...

Which is most reactive in base cataysed hydroysis reaction?

A

B

C

D

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To determine which compound is the most reactive in a base-catalyzed hydrolysis reaction, we need to analyze the reactivity of the four amides based on the presence of electron-withdrawing and electron-donating groups. ### Step-by-Step Solution: 1. **Identify the Compounds**: We have four amides to consider: - **Compound A**: Benzamide with a nitro group (NO2) - **Compound B**: Benzamide with a methoxy group (OCH3) - **Compound C**: Benzamide with a meta-substituted group - **Compound D**: Simple benzamide without any substituents 2. **Understand the Role of Electron-Withdrawing and Electron-Donating Groups**: - Electron-withdrawing groups (EWGs) increase the reactivity of the amide by stabilizing the negative charge that develops during the hydrolysis reaction. - Electron-donating groups (EDGs) decrease the reactivity of the amide by destabilizing the negative charge. 3. **Analyze Each Compound**: - **Compound A (NO2)**: The nitro group is a strong electron-withdrawing group (both -I and -R effects). This will significantly enhance the reactivity of the amide. - **Compound B (OCH3)**: The methoxy group is an electron-donating group (+R effect) and has a weak -I effect. This will decrease the reactivity of the amide. - **Compound C**: The meta-substituted group is less effective than the para or ortho positions for resonance but may have some -I effect depending on the specific group. - **Compound D**: This compound has no substituents, making it less reactive compared to compound A. 4. **Determine the Order of Reactivity**: Based on the analysis, the order of reactivity in base-catalyzed hydrolysis is influenced by the strength of the electron-withdrawing groups: - **Most Reactive**: Compound A (with NO2) - **Less Reactive**: Compound C (depending on the specific group) - **Even Less Reactive**: Compound D (no substituents) - **Least Reactive**: Compound B (with OCH3) 5. **Conclusion**: Therefore, the most reactive compound in base-catalyzed hydrolysis is **Compound A** (the one with the nitro group).

To determine which compound is the most reactive in a base-catalyzed hydrolysis reaction, we need to analyze the reactivity of the four amides based on the presence of electron-withdrawing and electron-donating groups. ### Step-by-Step Solution: 1. **Identify the Compounds**: We have four amides to consider: - **Compound A**: Benzamide with a nitro group (NO2) - **Compound B**: Benzamide with a methoxy group (OCH3) ...
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A2Z-ALDEHYDES, KETONES AND CARBOXYLIC ACID-Derivatives Of Carboxylic Acid
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  8. In the reaction the structure of the product T is:

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