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A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:
  • a)
  • b)
  • c)
  • d)
Correct answer is option 'D'. Can you explain this answer?
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A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:a)b)c)d)Correct answer is option 'D'. Can you explain this answer?
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A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:a)b)c)d)Correct answer is option 'D'. Can you explain this answer? for IIT JAM 2024 is part of IIT JAM preparation. The Question and answers have been prepared according to the IIT JAM exam syllabus. Information about A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:a)b)c)d)Correct answer is option 'D'. Can you explain this answer? covers all topics & solutions for IIT JAM 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:a)b)c)d)Correct answer is option 'D'. Can you explain this answer?.
Solutions for A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:a)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 IIT JAM. Download more important topics, notes, lectures and mock test series for IIT JAM Exam by signing up for free.
Here you can find the meaning of A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:a)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 A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:a)b)c)d)Correct answer is option 'D'. Can you explain this answer?, a detailed solution for A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:a)b)c)d)Correct answer is option 'D'. Can you explain this answer? has been provided alongside types of A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:a)b)c)d)Correct answer is option 'D'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice A ketone on treatment with bromine in methanol gives the corresponding monobromo compound [P] having molecular formula C5H9BrO. The compound [P] when treated with sodium methoxide in methanol produces [Q] as the major product, the 1H NMR spectrum data for compound [P] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound P and Q , respectively is:a)b)c)d)Correct answer is option 'D'. Can you explain this answer? tests, examples and also practice IIT JAM tests.
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