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Passage IIA chiral organic compound A (C9H12O2) does not give positive Tollens test or iodoform test. However, A on treatment with 1.0 equivalent of CH3MgBr followed by acid hydrolysis gives B (C10H16O2) which gives positive iodoform test. B on refluxing with aqueous Na2CO3 solution gives the following compound as major product.Q.If compound B is treated with excess of CH3MgBr followed by acid hydrolysis, how many different alcohols would be obtained?a)2b)3c)4d)8Correct answer is option 'C'. Can you explain this answer? for JEE 2024 is part of JEE preparation. The Question and answers have been prepared according to the JEE exam syllabus. Information about Passage IIA chiral organic compound A (C9H12O2) does not give positive Tollens test or iodoform test. However, A on treatment with 1.0 equivalent of CH3MgBr followed by acid hydrolysis gives B (C10H16O2) which gives positive iodoform test. B on refluxing with aqueous Na2CO3 solution gives the following compound as major product.Q.If compound B is treated with excess of CH3MgBr followed by acid hydrolysis, how many different alcohols would be obtained?a)2b)3c)4d)8Correct answer is option 'C'. Can you explain this answer? covers all topics & solutions for JEE 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for Passage IIA chiral organic compound A (C9H12O2) does not give positive Tollens test or iodoform test. However, A on treatment with 1.0 equivalent of CH3MgBr followed by acid hydrolysis gives B (C10H16O2) which gives positive iodoform test. B on refluxing with aqueous Na2CO3 solution gives the following compound as major product.Q.If compound B is treated with excess of CH3MgBr followed by acid hydrolysis, how many different alcohols would be obtained?a)2b)3c)4d)8Correct answer is option 'C'. Can you explain this answer?.

Solutions for Passage IIA chiral organic compound A (C9H12O2) does not give positive Tollens test or iodoform test. However, A on treatment with 1.0 equivalent of CH3MgBr followed by acid hydrolysis gives B (C10H16O2) which gives positive iodoform test. B on refluxing with aqueous Na2CO3 solution gives the following compound as major product.Q.If compound B is treated with excess of CH3MgBr followed by acid hydrolysis, how many different alcohols would be obtained?a)2b)3c)4d)8Correct answer is option 'C'. Can you explain this answer? in English & in Hindi are available as part of our courses for JEE. Download more important topics, notes, lectures and mock test series for JEE Exam by signing up for free.

Here you can find the meaning of Passage IIA chiral organic compound A (C9H12O2) does not give positive Tollens test or iodoform test. However, A on treatment with 1.0 equivalent of CH3MgBr followed by acid hydrolysis gives B (C10H16O2) which gives positive iodoform test. B on refluxing with aqueous Na2CO3 solution gives the following compound as major product.Q.If compound B is treated with excess of CH3MgBr followed by acid hydrolysis, how many different alcohols would be obtained?a)2b)3c)4d)8Correct answer is option 'C'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of Passage IIA chiral organic compound A (C9H12O2) does not give positive Tollens test or iodoform test. However, A on treatment with 1.0 equivalent of CH3MgBr followed by acid hydrolysis gives B (C10H16O2) which gives positive iodoform test. B on refluxing with aqueous Na2CO3 solution gives the following compound as major product.Q.If compound B is treated with excess of CH3MgBr followed by acid hydrolysis, how many different alcohols would be obtained?a)2b)3c)4d)8Correct answer is option 'C'. Can you explain this answer?, a detailed solution for Passage IIA chiral organic compound A (C9H12O2) does not give positive Tollens test or iodoform test. However, A on treatment with 1.0 equivalent of CH3MgBr followed by acid hydrolysis gives B (C10H16O2) which gives positive iodoform test. B on refluxing with aqueous Na2CO3 solution gives the following compound as major product.Q.If compound B is treated with excess of CH3MgBr followed by acid hydrolysis, how many different alcohols would be obtained?a)2b)3c)4d)8Correct answer is option 'C'. Can you explain this answer? has been provided alongside types of Passage IIA chiral organic compound A (C9H12O2) does not give positive Tollens test or iodoform test. However, A on treatment with 1.0 equivalent of CH3MgBr followed by acid hydrolysis gives B (C10H16O2) which gives positive iodoform test. B on refluxing with aqueous Na2CO3 solution gives the following compound as major product.Q.If compound B is treated with excess of CH3MgBr followed by acid hydrolysis, how many different alcohols would be obtained?a)2b)3c)4d)8Correct answer is option 'C'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice Passage IIA chiral organic compound A (C9H12O2) does not give positive Tollens test or iodoform test. However, A on treatment with 1.0 equivalent of CH3MgBr followed by acid hydrolysis gives B (C10H16O2) which gives positive iodoform test. B on refluxing with aqueous Na2CO3 solution gives the following compound as major product.Q.If compound B is treated with excess of CH3MgBr followed by acid hydrolysis, how many different alcohols would be obtained?a)2b)3c)4d)8Correct answer is option 'C'. Can you explain this answer? tests, examples and also practice JEE tests.