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A ketone on treatment with bromine in methanol gives the corresponding Monobromo compound [X] having molecular formula C5H9BrO. The compound [X] when treated with Sodium methoxide in methanol produces [Y] as the major product, the 1H NMR spectrum data for compound [X] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound X and Y, respectively, are:a)b)c)d)None of themCorrect answer is option 'D'. Can you explain this answer? for Chemistry 2024 is part of Chemistry preparation. The Question and answers have been prepared according to the Chemistry exam syllabus. Information about A ketone on treatment with bromine in methanol gives the corresponding Monobromo compound [X] having molecular formula C5H9BrO. The compound [X] when treated with Sodium methoxide in methanol produces [Y] as the major product, the 1H NMR spectrum data for compound [X] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound X and Y, respectively, are:a)b)c)d)None of themCorrect answer is option 'D'. Can you explain this answer? covers all topics & solutions for Chemistry 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 [X] having molecular formula C5H9BrO. The compound [X] when treated with Sodium methoxide in methanol produces [Y] as the major product, the 1H NMR spectrum data for compound [X] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound X and Y, respectively, are:a)b)c)d)None of themCorrect answer is option 'D'. Can you explain this answer?.

Solutions for A ketone on treatment with bromine in methanol gives the corresponding Monobromo compound [X] having molecular formula C5H9BrO. The compound [X] when treated with Sodium methoxide in methanol produces [Y] as the major product, the 1H NMR spectrum data for compound [X] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound X and Y, respectively, are:a)b)c)d)None of themCorrect answer is option 'D'. Can you explain this answer? in English & in Hindi are available as part of our courses for Chemistry. Download more important topics, notes, lectures and mock test series for Chemistry 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 [X] having molecular formula C5H9BrO. The compound [X] when treated with Sodium methoxide in methanol produces [Y] as the major product, the 1H NMR spectrum data for compound [X] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound X and Y, respectively, are:a)b)c)d)None of themCorrect 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 [X] having molecular formula C5H9BrO. The compound [X] when treated with Sodium methoxide in methanol produces [Y] as the major product, the 1H NMR spectrum data for compound [X] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound X and Y, respectively, are:a)b)c)d)None of themCorrect 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 [X] having molecular formula C5H9BrO. The compound [X] when treated with Sodium methoxide in methanol produces [Y] as the major product, the 1H NMR spectrum data for compound [X] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound X and Y, respectively, are:a)b)c)d)None of themCorrect 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 [X] having molecular formula C5H9BrO. The compound [X] when treated with Sodium methoxide in methanol produces [Y] as the major product, the 1H NMR spectrum data for compound [X] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound X and Y, respectively, are:a)b)c)d)None of themCorrect 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 [X] having molecular formula C5H9BrO. The compound [X] when treated with Sodium methoxide in methanol produces [Y] as the major product, the 1H NMR spectrum data for compound [X] are: 1H NMR:δ 1.17 (d, 6H), 3.02 (m, 1H), 4.10 (s, 2H). The compound X and Y, respectively, are:a)b)c)d)None of themCorrect answer is option 'D'. Can you explain this answer? tests, examples and also practice Chemistry tests.