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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
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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.
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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.
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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.