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Passage IAn unknown organic compound A is determined to have molecular formula C6H12Oand passing it through chiral column does not separate it into enantiomers. A does not react with Br2 nor with cold, dilute alkaline KMnO4. Heating A with concentrated H2SO4 gives product B (C6H10) which can be separated into enantiomers. Ozonolysis of a single enantiomer of B produces C, an optically active keto-aldehyde of formula C6H10O2 which gives positive iodoform test.Q.The correct statement regarding the outcome of the following reaction isa)X is an enantiomer of Ab)X is a diastereomer of Ac)If a pure enantiomer of B is taken, X could consist of a pair of diastereomersd)If a pure enantiomer of B is taken, X would be a racemic mixtureCorrect answer is option 'C'. Can you explain this answer? for Class 12 2024 is part of Class 12 preparation. The Question and answers have been prepared according to the Class 12 exam syllabus. Information about Passage IAn unknown organic compound A is determined to have molecular formula C6H12Oand passing it through chiral column does not separate it into enantiomers. A does not react with Br2 nor with cold, dilute alkaline KMnO4. Heating A with concentrated H2SO4 gives product B (C6H10) which can be separated into enantiomers. Ozonolysis of a single enantiomer of B produces C, an optically active keto-aldehyde of formula C6H10O2 which gives positive iodoform test.Q.The correct statement regarding the outcome of the following reaction isa)X is an enantiomer of Ab)X is a diastereomer of Ac)If a pure enantiomer of B is taken, X could consist of a pair of diastereomersd)If a pure enantiomer of B is taken, X would be a racemic mixtureCorrect answer is option 'C'. Can you explain this answer? covers all topics & solutions for Class 12 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for Passage IAn unknown organic compound A is determined to have molecular formula C6H12Oand passing it through chiral column does not separate it into enantiomers. A does not react with Br2 nor with cold, dilute alkaline KMnO4. Heating A with concentrated H2SO4 gives product B (C6H10) which can be separated into enantiomers. Ozonolysis of a single enantiomer of B produces C, an optically active keto-aldehyde of formula C6H10O2 which gives positive iodoform test.Q.The correct statement regarding the outcome of the following reaction isa)X is an enantiomer of Ab)X is a diastereomer of Ac)If a pure enantiomer of B is taken, X could consist of a pair of diastereomersd)If a pure enantiomer of B is taken, X would be a racemic mixtureCorrect answer is option 'C'. Can you explain this answer?.

Solutions for Passage IAn unknown organic compound A is determined to have molecular formula C6H12Oand passing it through chiral column does not separate it into enantiomers. A does not react with Br2 nor with cold, dilute alkaline KMnO4. Heating A with concentrated H2SO4 gives product B (C6H10) which can be separated into enantiomers. Ozonolysis of a single enantiomer of B produces C, an optically active keto-aldehyde of formula C6H10O2 which gives positive iodoform test.Q.The correct statement regarding the outcome of the following reaction isa)X is an enantiomer of Ab)X is a diastereomer of Ac)If a pure enantiomer of B is taken, X could consist of a pair of diastereomersd)If a pure enantiomer of B is taken, X would be a racemic mixtureCorrect answer is option 'C'. Can you explain this answer? in English & in Hindi are available as part of our courses for Class 12. Download more important topics, notes, lectures and mock test series for Class 12 Exam by signing up for free.

Here you can find the meaning of Passage IAn unknown organic compound A is determined to have molecular formula C6H12Oand passing it through chiral column does not separate it into enantiomers. A does not react with Br2 nor with cold, dilute alkaline KMnO4. Heating A with concentrated H2SO4 gives product B (C6H10) which can be separated into enantiomers. Ozonolysis of a single enantiomer of B produces C, an optically active keto-aldehyde of formula C6H10O2 which gives positive iodoform test.Q.The correct statement regarding the outcome of the following reaction isa)X is an enantiomer of Ab)X is a diastereomer of Ac)If a pure enantiomer of B is taken, X could consist of a pair of diastereomersd)If a pure enantiomer of B is taken, X would be a racemic mixtureCorrect answer is option 'C'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of Passage IAn unknown organic compound A is determined to have molecular formula C6H12Oand passing it through chiral column does not separate it into enantiomers. A does not react with Br2 nor with cold, dilute alkaline KMnO4. Heating A with concentrated H2SO4 gives product B (C6H10) which can be separated into enantiomers. Ozonolysis of a single enantiomer of B produces C, an optically active keto-aldehyde of formula C6H10O2 which gives positive iodoform test.Q.The correct statement regarding the outcome of the following reaction isa)X is an enantiomer of Ab)X is a diastereomer of Ac)If a pure enantiomer of B is taken, X could consist of a pair of diastereomersd)If a pure enantiomer of B is taken, X would be a racemic mixtureCorrect answer is option 'C'. Can you explain this answer?, a detailed solution for Passage IAn unknown organic compound A is determined to have molecular formula C6H12Oand passing it through chiral column does not separate it into enantiomers. A does not react with Br2 nor with cold, dilute alkaline KMnO4. Heating A with concentrated H2SO4 gives product B (C6H10) which can be separated into enantiomers. Ozonolysis of a single enantiomer of B produces C, an optically active keto-aldehyde of formula C6H10O2 which gives positive iodoform test.Q.The correct statement regarding the outcome of the following reaction isa)X is an enantiomer of Ab)X is a diastereomer of Ac)If a pure enantiomer of B is taken, X could consist of a pair of diastereomersd)If a pure enantiomer of B is taken, X would be a racemic mixtureCorrect answer is option 'C'. Can you explain this answer? has been provided alongside types of Passage IAn unknown organic compound A is determined to have molecular formula C6H12Oand passing it through chiral column does not separate it into enantiomers. A does not react with Br2 nor with cold, dilute alkaline KMnO4. Heating A with concentrated H2SO4 gives product B (C6H10) which can be separated into enantiomers. Ozonolysis of a single enantiomer of B produces C, an optically active keto-aldehyde of formula C6H10O2 which gives positive iodoform test.Q.The correct statement regarding the outcome of the following reaction isa)X is an enantiomer of Ab)X is a diastereomer of Ac)If a pure enantiomer of B is taken, X could consist of a pair of diastereomersd)If a pure enantiomer of B is taken, X would be a racemic mixtureCorrect answer is option 'C'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice Passage IAn unknown organic compound A is determined to have molecular formula C6H12Oand passing it through chiral column does not separate it into enantiomers. A does not react with Br2 nor with cold, dilute alkaline KMnO4. Heating A with concentrated H2SO4 gives product B (C6H10) which can be separated into enantiomers. Ozonolysis of a single enantiomer of B produces C, an optically active keto-aldehyde of formula C6H10O2 which gives positive iodoform test.Q.The correct statement regarding the outcome of the following reaction isa)X is an enantiomer of Ab)X is a diastereomer of Ac)If a pure enantiomer of B is taken, X could consist of a pair of diastereomersd)If a pure enantiomer of B is taken, X would be a racemic mixtureCorrect answer is option 'C'. Can you explain this answer? tests, examples and also practice Class 12 tests.