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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? for Class 11 2024 is part of Class 11 preparation. The Question and answers have been prepared
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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.