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Comprehension TypeDirection (Q. Nos. 15-19) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Five 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 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.Structure of B that satisfy the above criteria isa)b)c)d)Correct answer is option 'D'. 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 Comprehension TypeDirection (Q. Nos. 15-19) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Five 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 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.Structure of B that satisfy the above criteria isa)b)c)d)Correct answer is option 'D'. 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 Comprehension TypeDirection (Q. Nos. 15-19) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Five 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 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.Structure of B that satisfy the above criteria isa)b)c)d)Correct answer is option 'D'. Can you explain this answer?.

Solutions for Comprehension TypeDirection (Q. Nos. 15-19) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Five 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 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.Structure of B that satisfy the above criteria isa)b)c)d)Correct answer is option 'D'. 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 Comprehension TypeDirection (Q. Nos. 15-19) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Five 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 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.Structure of B that satisfy the above criteria isa)b)c)d)Correct answer is option 'D'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of Comprehension TypeDirection (Q. Nos. 15-19) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Five 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 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.Structure of B that satisfy the above criteria isa)b)c)d)Correct answer is option 'D'. Can you explain this answer?, a detailed solution for Comprehension TypeDirection (Q. Nos. 15-19) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Five 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 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.Structure of B that satisfy the above criteria isa)b)c)d)Correct answer is option 'D'. Can you explain this answer? has been provided alongside types of Comprehension TypeDirection (Q. Nos. 15-19) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Five 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 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.Structure of B that satisfy the above criteria isa)b)c)d)Correct answer is option 'D'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice Comprehension TypeDirection (Q. Nos. 15-19) This section contains 2 paragraphs, each describing theory, experiments, data, etc. Five 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 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.Structure of B that satisfy the above criteria isa)b)c)d)Correct answer is option 'D'. Can you explain this answer? tests, examples and also practice Class 12 tests.