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In which of the following compound elect...

In which of the following compound electrophilic aromatic substitution take place in phenyl ring present in left hand side ?

A

B

C

D

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To determine which compound allows for electrophilic aromatic substitution (EAS) to occur on the phenyl ring present on the left-hand side, we need to analyze the substituents attached to the aromatic rings in each option. Here’s a step-by-step solution: ### Step 1: Understand Electrophilic Aromatic Substitution (EAS) Electrophilic aromatic substitution occurs when an electrophile attacks an aromatic ring. The reaction is favored by electron-rich aromatic systems, as they can stabilize the positive charge that develops during the reaction. ### Step 2: Identify Electron-Donating and Electron-Withdrawing Groups - **Electron-Donating Groups (EDGs)**: These groups increase the electron density of the aromatic ring, making it more reactive towards electrophiles. Common EDGs include -OH, -OCH₃, -NH₂, etc. - **Electron-Withdrawing Groups (EWGs)**: These groups decrease the electron density of the aromatic ring, making it less reactive towards electrophiles. Common EWGs include -NO₂, -CN, -COOH, etc. ### Step 3: Analyze Each Compound Let’s consider the four options one by one: 1. **Option 1**: Contains an electron-donating group on the left ring and an electron-withdrawing group on the right ring. The left ring becomes electron-rich, but the right ring is more electron-rich due to the EDG. EAS will occur on the right ring. 2. **Option 2**: Similar to option 1, the left ring has an EDG, but the right ring is more electron-rich. EAS will occur on the right ring. 3. **Option 3**: Again, the left ring has an EDG, while the right ring is more electron-rich. EAS will occur on the right ring. 4. **Option 4**: The left ring has an electron-withdrawing group, making it electron-deficient, while the right ring has an EDG, making it electron-rich. In this case, the left ring is more electron-rich than the right ring due to the presence of the EDG on the left ring, allowing EAS to occur on the left ring. ### Step 4: Conclusion Based on the analysis, the only compound where electrophilic aromatic substitution occurs on the left-hand side phenyl ring is **Option 4**. ### Final Answer **Option 4** is the correct choice where electrophilic aromatic substitution takes place in the phenyl ring present on the left-hand side. ---

To determine which compound allows for electrophilic aromatic substitution (EAS) to occur on the phenyl ring present on the left-hand side, we need to analyze the substituents attached to the aromatic rings in each option. Here’s a step-by-step solution: ### Step 1: Understand Electrophilic Aromatic Substitution (EAS) Electrophilic aromatic substitution occurs when an electrophile attacks an aromatic ring. The reaction is favored by electron-rich aromatic systems, as they can stabilize the positive charge that develops during the reaction. ### Step 2: Identify Electron-Donating and Electron-Withdrawing Groups - **Electron-Donating Groups (EDGs)**: These groups increase the electron density of the aromatic ring, making it more reactive towards electrophiles. Common EDGs include -OH, -OCH₃, -NH₂, etc. - **Electron-Withdrawing Groups (EWGs)**: These groups decrease the electron density of the aromatic ring, making it less reactive towards electrophiles. Common EWGs include -NO₂, -CN, -COOH, etc. ...
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  • Which of the following compounds are aromatic ?

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    B
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    C
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  • Which of the following compounds exhibit aromatic character?

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