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Statement I: In strongly acidic solution...

Statement I: In strongly acidic solutions , anline becomes more reactive towards electrophilic reagents Statement II: The amino group being completely protonated in strongly acidic solution, the lone pair of electrons on nitrogen is no longer available for resonance.

A

Both Assertion and Reason are true and Reason is the correct explanation of Assertion.

B

Both Assertion and Reason are true but Reason is not correct explanation of Assertion.

C

Assertion is true but Reason is false.

D

Assertion is false but Reason is true.

Text Solution

Verified by Experts

The correct Answer is:
D
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RESONANCE-AROMATIC COMPOUNDS-Exercise-3 (Part-I) JEE Advanced
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  2. How would you synthesise 4-methoxyphenol from bromobenzene in not mo...

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  3. Write structures of the products A, B,C,D and E in the following schem...

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  4. Convert

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  5. How would you carry out the following conversion efficiently using NOT...

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  6. Identify A, B, C, D and write the balanced chemical equations of forma...

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  7. under Hofmann conditions will give :

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  8. Which reagent (X) is used to convert I to II

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  9. Consider the pathway of a well known organic reaction Which step ...

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  10. CH(3)NH(2)+CHCl(3)+KOH to Nitrogen containing compound +KCl + H(2)O.

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  11. What are P & Q.

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  12. Reimer-Tiemann reaction introduces an aldehyde group on to the aromati...

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  13. Reimer-Tiemann reaction introduces an aldehyde group on to the aromati...

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  14. Reimer-Tiemann reaction introduces an aldehyde group on to the aromati...

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  15. In the reaction the intermediate(s) is/are:

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  16. Match the reactions in Column I with appropriate options in Column II.

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  17. The major product of the following reaction is :

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  18. Amongst the compounds gives, the one that would form a brilliant color...

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  19. In the following reacation. The product(s) formed is/are

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  20. The major product(s) of the following reaction is (are)

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