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Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).
Passage I
An unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.
Q. The correct statement concerning X is
- a)It is chiral
- b)It has a pair of diastereomer
- c)It is a tertiary bromide
- d)With (CH3)3COK in tertiary butanol, an isomer of Y is formed
Correct answer is option 'B'. Can you explain this answer?
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Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each des...
Explanation:
The given compound X (C5HgBr) does not decolourize the purple color of alkaline permanganate solution. It reacts with C2H5OK/C2H5OH to form a compound Y (C5H8) as the only structural isomer. Upon further reactions, Y gives Z (C5H8O2), which can exist as a pair of enantiomers.
Key Points:
- Compound X does not decolourize the purple color of alkaline permanganate solution.
- Compound Y is the only structural isomer of X and has the formula C5H8.
- Catalytic hydrogenation of Y gives methyl cyclobutane.
- Ozonolysis of Y gives Z (C5H8O2), which can exist as a pair of enantiomers.
Analysis:
The correct statement concerning X is that it has a pair of diastereomers.
Reasoning:
- The compound X (C5HgBr) does not decolourize the purple color of alkaline permanganate solution. This indicates that X is not an alkene or alkyne, as these functional groups would react with permanganate to produce a color change.
- The compound Y (C5H8) is the only structural isomer of X. This implies that X must have a double bond, as Y is an alkene. The presence of a double bond in X suggests that it is an alkene.
- Catalytic hydrogenation of Y gives methyl cyclobutane. This indicates that Y has a double bond which can be reduced to form a cyclobutane ring. This confirms that Y is an alkene.
- Ozonolysis of Y gives Z (C5H8O2), which can exist as a pair of enantiomers. This implies that Y must have a chiral center. A chiral center is a carbon atom bonded to four different groups. Since Y is an alkene, it must have a chiral center at one of the carbon atoms of the double bond.
- Therefore, X is an alkene with a chiral center, indicating that it has a pair of diastereomers.
Conclusion:
The correct statement concerning X is that it has a pair of diastereomers.
The given compound X (C5HgBr) does not decolourize the purple color of alkaline permanganate solution. It reacts with C2H5OK/C2H5OH to form a compound Y (C5H8) as the only structural isomer. Upon further reactions, Y gives Z (C5H8O2), which can exist as a pair of enantiomers.
Key Points:
- Compound X does not decolourize the purple color of alkaline permanganate solution.
- Compound Y is the only structural isomer of X and has the formula C5H8.
- Catalytic hydrogenation of Y gives methyl cyclobutane.
- Ozonolysis of Y gives Z (C5H8O2), which can exist as a pair of enantiomers.
Analysis:
The correct statement concerning X is that it has a pair of diastereomers.
Reasoning:
- The compound X (C5HgBr) does not decolourize the purple color of alkaline permanganate solution. This indicates that X is not an alkene or alkyne, as these functional groups would react with permanganate to produce a color change.
- The compound Y (C5H8) is the only structural isomer of X. This implies that X must have a double bond, as Y is an alkene. The presence of a double bond in X suggests that it is an alkene.
- Catalytic hydrogenation of Y gives methyl cyclobutane. This indicates that Y has a double bond which can be reduced to form a cyclobutane ring. This confirms that Y is an alkene.
- Ozonolysis of Y gives Z (C5H8O2), which can exist as a pair of enantiomers. This implies that Y must have a chiral center. A chiral center is a carbon atom bonded to four different groups. Since Y is an alkene, it must have a chiral center at one of the carbon atoms of the double bond.
- Therefore, X is an alkene with a chiral center, indicating that it has a pair of diastereomers.
Conclusion:
The correct statement concerning X is that it has a pair of diastereomers.
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Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each des...
B D is correct.
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Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. Can you explain this answer?
Question Description
Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. 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 Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. 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 Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. Can you explain this answer?.
Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. 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 Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. 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 Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. Can you explain this answer?.
Solutions for Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. Can you explain this answer? in English & in Hindi are available as part of our courses for Class 11.
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Here you can find the meaning of Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of
Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. Can you explain this answer?, a detailed solution for Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. Can you explain this answer? has been provided alongside types of Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. Can you explain this answer? theory, EduRev gives you an
ample number of questions to practice Direction (Q. Nos. 10-14) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Six questions related to the paragraphs have been given. Each question has only one correct answer among the four given options (a), (b), (c) and (d).Passage IAn unknown compound X (C5HgBr) does not decolourise purple colour of alkaline permanganate solution. Upon treatment with C2H5OK/C2H5OH, X gives Y (C5H8) as only structural isomer. Catalytic hydrogenation of Y gives methyl cyclobutane. Ozonolysis of Y gives Z (C5H8O2) which can exist as a pair of enantiomers.Q.The correct statement concerning X isa)It is chiralb)It has a pair of diastereomerc)It is a tertiary bromided)With (CH3)3COK in tertiary butanol, an isomer of Y is formedCorrect answer is option 'B'. Can you explain this answer? tests, examples and also practice Class 11 tests.
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