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Which one the most reactive towards elec...

Which one the most reactive towards electrophilic reagent:

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B

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To determine which compound is the most reactive towards electrophilic reagents, we need to analyze the electron-donating and electron-withdrawing effects of the substituents attached to the benzene ring in each compound. Here’s a step-by-step breakdown of the reasoning: ### Step 1: Identify the Compounds We have four compounds with a benzene ring and various substituents. The substituents include: 1. Ethyl group (Et) and a nitrogen atom (NH) attached to a carbonyl (C=O) and a methyl group (CH3). 2. Ethyl group (Et) and a hydroxyl group (OH) attached to a methylene (CH2). 3. Ethyl group (Et), a carbonyl (C=O), and a methyl group (CH3). 4. Ethyl group (Et) and a methoxy group (OCH3). ### Step 2: Analyze Each Compound - **Compound 1**: The nitrogen has a lone pair that can participate in resonance (donate electrons) but is weakened by the electron-withdrawing effect of the carbonyl group. Thus, it has a moderate +M effect and a +I effect from the ethyl group. - **Compound 2**: The hydroxyl group (OH) has lone pairs but acts as an electron-withdrawing group due to its -I effect. The ethyl group contributes a +I effect. The overall effect is a weaker electron density on the benzene ring. - **Compound 3**: Similar to compound 1, the carbonyl (C=O) can withdraw electrons, but the ethyl group still contributes a +I effect. The resonance effect is similar, leading to moderate reactivity. - **Compound 4**: The methoxy group (OCH3) has a strong +M effect due to the lone pairs on oxygen being able to donate electrons into the benzene ring. The ethyl group contributes a +I effect, enhancing the electron density on the ring. ### Step 3: Compare the Effects - The strongest electron-donating group (which enhances reactivity towards electrophiles) is the methoxy group in compound 4. - The other compounds have weaker electron-donating effects due to the presence of electron-withdrawing groups (like carbonyls and hydroxyls). ### Conclusion Based on the analysis of the electron-donating and withdrawing effects of the substituents, **Compound 4 (with the OCH3 group)** is the most reactive towards electrophilic reagents due to its strong +M effect. ### Final Answer The most reactive compound towards electrophilic reagents is **Compound 4 (OCH3)**. ---
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