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7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) because

  • a)
    C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadiene

  • b)
    7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cation

  • c)
    7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cation

  • d)
    Both ionises to form anions but one form aromatic while other form anti-aromatic anion

Correct answer is option 'C'. Can you explain this answer?
Verified Answer
7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solu...
The correct answer is Option C.
The C-Br bond in the case of 7-bromo-1, 3, 5-cycloheptatriene is broken easily because the intermediate carbocation formed is very stable (aromatic as it contains (4n + 2)π e- ie, follows Huckle rule) while it does not break easily in the case of S-bromo-1, 3-cyclopentadiene because carbocation formed here is highly unstable as it is anti aromatic ie, does not follow Huckel rule. (It contains 4π electrons).
 
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Most Upvoted Answer
7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solu...
Explanation:

7-bromo-1,3,5-cycloheptatriene:
- 7-bromo-1,3,5-cycloheptatriene is an aromatic compound due to the presence of a continuous conjugated system of π electrons in the ring.
- When it ionizes in aqueous solution, it forms an aromatic cation which is relatively stable.

5-bromo-1,3-cyclopentadiene:
- 5-bromo-1,3-cyclopentadiene, on the other hand, does not form an aromatic system when ionized in aqueous solution.
- The ionized form would result in a highly unstable anti-aromatic cation due to the presence of 4n π electrons in the cyclic system.

Comparison:
- The key difference lies in the aromaticity of the resulting ions upon ionization.
- 7-bromo-1,3,5-cycloheptatriene forms an aromatic cation, making it relatively stable in aqueous solution.
- 5-bromo-1,3-cyclopentadiene, however, forms a highly unstable anti-aromatic cation, preventing it from ionizing in the same way as the former compound.
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7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) becausea)C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadieneb)7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cationc)7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cationd)Both ionises to form anions but one form aromatic while other form anti-aromatic anionCorrect answer is option 'C'. Can you explain this answer?
Question Description
7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) becausea)C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadieneb)7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cationc)7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cationd)Both ionises to form anions but one form aromatic while other form anti-aromatic anionCorrect answer is option 'C'. Can you explain this answer? for Class 11 2024 is part of Class 11 preparation. The Question and answers have been prepared according to the Class 11 exam syllabus. Information about 7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) becausea)C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadieneb)7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cationc)7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cationd)Both ionises to form anions but one form aromatic while other form anti-aromatic anionCorrect answer is option 'C'. Can you explain this answer? covers all topics & solutions for Class 11 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for 7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) becausea)C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadieneb)7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cationc)7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cationd)Both ionises to form anions but one form aromatic while other form anti-aromatic anionCorrect answer is option 'C'. Can you explain this answer?.
Solutions for 7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) becausea)C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadieneb)7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cationc)7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cationd)Both ionises to form anions but one form aromatic while other form anti-aromatic anionCorrect answer is option 'C'. Can you explain this answer? in English & in Hindi are available as part of our courses for Class 11. Download more important topics, notes, lectures and mock test series for Class 11 Exam by signing up for free.
Here you can find the meaning of 7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) becausea)C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadieneb)7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cationc)7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cationd)Both ionises to form anions but one form aromatic while other form anti-aromatic anionCorrect answer is option 'C'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of 7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) becausea)C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadieneb)7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cationc)7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cationd)Both ionises to form anions but one form aromatic while other form anti-aromatic anionCorrect answer is option 'C'. Can you explain this answer?, a detailed solution for 7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) becausea)C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadieneb)7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cationc)7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cationd)Both ionises to form anions but one form aromatic while other form anti-aromatic anionCorrect answer is option 'C'. Can you explain this answer? has been provided alongside types of 7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) becausea)C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadieneb)7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cationc)7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cationd)Both ionises to form anions but one form aromatic while other form anti-aromatic anionCorrect answer is option 'C'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice 7-bromo-1,3,5-cycloheptatriene exists as ionic species in aqueous solution while 5-bromo-1,3-cyclopentadiene does not ionise even in presence of AgNO3(aq) becausea)C—Br bond has partial double bond character in 5-bromo-1,3-cyclopentadieneb)7-bromo-1,3,5-cyclopheptatriene ionises to form an aromatic anion while 5-bromo-1,3-cyclopentadiene ionises to form an anti-aromatic cationc)7-bromo-1,3,5-cycloheptatriene ionises into an aromatic cation while 5-bromo-1,3 cyclopentadiene ionises into a highly unstable anti-aromatic cationd)Both ionises to form anions but one form aromatic while other form anti-aromatic anionCorrect answer is option 'C'. Can you explain this answer? tests, examples and also practice Class 11 tests.
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